-
2
-
-
0347022226
-
Intestinal absorption of penclomedine from lipid vehicles in the conscious rat: Contribution of emulsification versus digestibility
-
de Smidt PC, Campanero MA, Troconiz IF. Intestinal absorption of penclomedine from lipid vehicles in the conscious rat: contribution of emulsification versus digestibility. Int J Pharm. 2004;270(1-2):109-118
-
(2004)
Int J Pharm.
, vol.270
, Issue.1-2
, pp. 109-118
-
-
De Smidt, P.C.1
Campanero, M.A.2
Troconiz, I.F.3
-
3
-
-
39149126301
-
Biopharmaceutical challenges associated with drugs with low aqueous solubility--the potential impact of lipidbased formulations
-
ODriscoll CM, Griffin BT. Biopharmaceutical challenges associated with drugs with low aqueous solubility--the potential impact of lipidbased formulations. Adv Drug Deliv Rev. 2008;60(6):617-624
-
(2008)
Adv Drug Deliv Rev.
, vol.60
, Issue.6
, pp. 617-624
-
-
Odriscoll, C.M.1
Griffin, B.T.2
-
4
-
-
33746541075
-
Enhancing mechanism of Labrasol on intestinal membrane permeability of the hydrophilic drug gentamicin sulfate
-
Koga K, Kusawake Y, Ito Y, Sugioka N, Shibata N, Takada K. Enhancing mechanism of Labrasol on intestinal membrane permeability of the hydrophilic drug gentamicin sulfate. Eur J Pharm Biopharm. 2006;64(1):82-91.
-
(2006)
Eur J Pharm Biopharm.
, vol.64
, Issue.1
, pp. 82-91
-
-
Koga, K.1
Kusawake, Y.2
Ito, Y.3
Sugioka, N.4
Shibata, N.5
Takada, K.6
-
5
-
-
15244353232
-
Effect of self-microemulsifying drug delivery systems containing Labrasol on tight junctions in Caco-2 cells
-
Sha X, Yan G, Wu Y, Li J, Fang X. Effect of self-microemulsifying drug delivery systems containing Labrasol on tight junctions in Caco-2 cells. Eur J Pharm Sci. 2005;24(5):477-486
-
(2005)
Eur J Pharm Sci.
, vol.24
, Issue.5
, pp. 477-486
-
-
Sha, X.1
Yan, G.2
Wu, Y.3
Li, J.4
Fang, X.5
-
6
-
-
33644789659
-
Effect of self-microemulsifying system on cell tight junctions
-
Jan
-
Sha XY, Fang XL. Effect of self-microemulsifying system on cell tight junctions. Yao Xue Xue Bao. 2006 Jan;41(1):30-35
-
(2006)
Yao Xue Xue Bao
, vol.41
, Issue.1
, pp. 30-35
-
-
Sha, X.Y.1
Fang, X.L.2
-
7
-
-
1242337284
-
Enhanced oral absorption of paclitaxel in a novel self-microemulsifying drug delivery system with or without concomitant use of P-glycoprotein inhibitors
-
Yang S, Gursoy RN, Lambert G, Benita S. Enhanced oral absorption of paclitaxel in a novel self-microemulsifying drug delivery system with or without concomitant use of P-glycoprotein inhibitors. Pharm Res. 2004;21(2):261-270
-
(2004)
Pharm Res.
, vol.21
, Issue.2
, pp. 261-270
-
-
Yang, S.1
Gursoy, R.N.2
Lambert, G.3
Benita, S.4
-
8
-
-
33847341135
-
Lipid formulation strategies for enhancing intestinal transport and absorption of P-glycoprotein (P-gp) substrate drugs: In vitro/in vivo case studies
-
Constantinides PP, Wasan KM. Lipid formulation strategies for enhancing intestinal transport and absorption of P-glycoprotein (P-gp) substrate drugs: in vitro/in vivo case studies. J Pharm Sci. 2007;96(2):235-248
-
(2007)
J Pharm Sci.
, vol.96
, Issue.2
, pp. 235-248
-
-
Constantinides, P.P.1
Wasan, K.M.2
-
9
-
-
0027287976
-
Effect of food and a monoglyceride emulsion formulation on danazol bioavailability
-
Charman WN, Rogge MC, Boddy AW, Berger BM. Effect of food and a monoglyceride emulsion formulation on danazol bioavailability. J. Clin. Pharmacol. 1993;33:381-386
-
(1993)
J. Clin. Pharmacol.
, vol.33
, pp. 381-386
-
-
Charman, W.N.1
Rogge, M.C.2
Boddy, A.W.3
Berger, B.M.4
-
10
-
-
0029825085
-
Effects of food on drug absorption
-
Welling PG. Effects of food on drug absorption. Ann. Rev. Nutr. 1996;16 383-415.
-
(1996)
Ann. Rev. Nutr.
, vol.16
, pp. 383-415
-
-
Welling, P.G.1
-
11
-
-
27644483201
-
The novel formulation design of O/W microemulsion for improving the gastrointestinal absorption of poorly water soluble compounds
-
Araya H, Tomita M, Hayashi M. The novel formulation design of O/W microemulsion for improving the gastrointestinal absorption of poorly water soluble compounds. Int J Pharm. 2005;305(1-2):61-74.
-
(2005)
Int J Pharm.
, vol.305
, Issue.1-2
, pp. 61-74
-
-
Araya, H.1
Tomita, M.2
Hayashi, M.3
-
12
-
-
34247609989
-
Development and bioavailability assessment of ramipril nanoemulsion formulation
-
DOI 10.1016/j.ejpb.2006.10.014, PII S0939641106002839
-
Shafiq S, Shakeel F, Talegaonkar S, Ahmad FJ, Khar RK, Ali M. Development and bioavailability assessment of ramipril nanoemulsion formulation. Eur J Pharm Biopharm. 2007;66(2):227-243 (Pubitemid 46667230)
-
(2007)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.66
, Issue.2
, pp. 227-243
-
-
Shafiq, S.1
Shakeel, F.2
Talegaonkar, S.3
Ahmad, F.J.4
Khar, R.K.5
Ali, M.6
-
13
-
-
0022999025
-
The oral absorption of cefoxitin from oil and emulsion vehicles in rats
-
Palin KJ, Phillips AJ, Ning A. The oral absorption of cefoxitin from oil and emulsion vehicles in rats. Int J Pharm. 1986;33:99-104.
-
(1986)
Int J Pharm.
, vol.33
, pp. 99-104
-
-
Palin, K.J.1
Phillips, A.J.2
Ning, A.3
-
14
-
-
0002890024
-
Improved oral bioavailability of an HIV protease inhibitor using Gelucire 44/14 and Labrasol vehicles
-
Aungst BJ, Nguyen N, Rogers NJ, Rowe S, Hussain M, Shum L, White SJ. Improved oral bioavailability of an HIV protease inhibitor using Gelucire 44/14 and Labrasol vehicles. SBT Gattefosse. 1994;87:49-54.
-
(1994)
SBT Gattefosse.
, vol.87
, pp. 49-54
-
-
Aungst, B.J.1
Nguyen, N.2
Rogers, N.J.3
Rowe, S.4
Hussain, M.5
Shum, L.6
White, S.J.7
-
15
-
-
0342617694
-
Lipid-based vehicles for the oral delivery of poorly water soluble drugs
-
Humberstone AJ, Charman WN. Lipid-based vehicles for the oral delivery of poorly water soluble drugs. Adv Drug Deliv Rev. 1997;25(1):103-128
-
(1997)
Adv Drug Deliv Rev.
, vol.25
, Issue.1
, pp. 103-128
-
-
Humberstone, A.J.1
Charman, W.N.2
-
16
-
-
0035940057
-
Intestinal lymphatic drug transport: An update
-
Porter CJ, Charman WN. Intestinal lymphatic drug transport: an update. Adv Drug Deliv Rev. 2001;50(1-2):61-80.
-
(2001)
Adv Drug Deliv Rev.
, vol.50
, Issue.1-2
, pp. 61-80
-
-
Porter, C.J.1
Charman, W.N.2
-
17
-
-
0026586447
-
Self-emulsifying drug delivery systems: Formulation and biopharmaceutic evaluation of an investigational lipophilic compound
-
Charman SA, Charman WN, Rogge MC, Wilson TD, Dutko FJ, Pouton CW. Self-emulsifying drug delivery systems: formulation and biopharmaceutic evaluation of an investigational lipophilic compound. Pharm Res. 1992;9(1):87-93.
-
(1992)
Pharm Res.
, vol.9
, Issue.1
, pp. 87-93
-
-
Charman, S.A.1
Charman, W.N.2
Rogge, M.C.3
Wilson, T.D.4
Dutko, F.J.5
Pouton, C.W.6
-
18
-
-
1842684453
-
Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs
-
Gursoy RN, Benita S. Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs. Biomed Pharmacother. 2004;58(3):173-182
-
(2004)
Biomed Pharmacother.
, vol.58
, Issue.3
, pp. 173-182
-
-
Gursoy, R.N.1
Benita, S.2
-
19
-
-
68949135410
-
Self micro-emulsifying drug delivery system: Formulation development and biopharmaceutical evaluation of lipophilic drugs
-
Patel D, Sawant KK. Self micro-emulsifying drug delivery system: formulation development and biopharmaceutical evaluation of lipophilic drugs. Curr Drug Deliv. 2009;6(4):419-424
-
(2009)
Curr Drug Deliv.
, vol.6
, Issue.4
, pp. 419-424
-
-
Patel, D.1
Sawant, K.K.2
-
21
-
-
13844296701
-
Pharmacokinetic characterization of different dose combinations of coadministered tipranavir and ritonavir in healthy volunteers
-
MacGregor TR, Sabo JP, Norris SH, Johnson P, Galitz L, McCallister S. Pharmacokinetic characterization of different dose combinations of coadministered tipranavir and ritonavir in healthy volunteers. HIV Clin Trials. 2004;5(6):371-382
-
(2004)
HIV Clin Trials.
, vol.5
, Issue.6
, pp. 371-382
-
-
MacGregor, T.R.1
Sabo, J.P.2
Norris, S.H.3
Johnson, P.4
Galitz, L.5
McCallister, S.6
-
22
-
-
1542409142
-
A 14-day dose-response study of the efficacy, safety, and pharmacokinetics of the nonpeptidic protease inhibitor tipranavir in treatment-naive HIV-1-infected patients
-
McCallister S, Valdez H, Curry K, MacGregor T, Borin M, Freimuth W, Wang Y, Mayers DL. A 14-day dose-response study of the efficacy, safety, and pharmacokinetics of the nonpeptidic protease inhibitor tipranavir in treatment-naive HIV-1-infected patients. J Acquir Immune Defic Syndr. 2004;35(4):376-382
-
(2004)
J Acquir Immune Defic Syndr.
, vol.35
, Issue.4
, pp. 376-382
-
-
McCallister, S.1
Valdez, H.2
Curry, K.3
MacGregor, T.4
Borin, M.5
Freimuth, W.6
Wang, Y.7
Mayers, D.L.8
-
23
-
-
39149113817
-
Formulation of lipid-based delivery systems for oral administration: Materials, methods and strategies
-
Pouton CW, Porter CJ. Formulation of lipid-based delivery systems for oral administration: materials, methods and strategies. Adv Drug Deliv Rev. 2008;60(6):625-637
-
(2008)
Adv Drug Deliv Rev.
, vol.60
, Issue.6
, pp. 625-637
-
-
Pouton, C.W.1
Porter, C.J.2
-
24
-
-
50549085646
-
Solid microemulsion preconcentrate (NanOsorb) of artemether for effective treatment of malaria
-
Joshi M, Pathak S, Sharma S, Patravale V. Solid microemulsion preconcentrate (NanOsorb) of artemether for effective treatment of malaria. Int J Pharm. 2008;362(1-2):172-178
-
(2008)
Int J Pharm.
, vol.362
, Issue.1-2
, pp. 172-178
-
-
Joshi, M.1
Pathak, S.2
Sharma, S.3
Patravale, V.4
-
25
-
-
0033805858
-
Lipid formulations for oral administration of drugs: Nonemulsifying, self-emulsifying and self-microemulsifying drug delivery systems
-
Pouton CW. Lipid formulations for oral administration of drugs: nonemulsifying, self-emulsifying and self-microemulsifying drug delivery systems. Eur J Pharm Sci. 2000;11(Suppl 2):S93-8.
-
(2000)
Eur J Pharm Sci.
, vol.11
, Issue.SUPPL. 2
-
-
Pouton, C.W.1
-
26
-
-
0343487750
-
Formulation of self-emulsifying drug delivery systems
-
Pouton CW. Formulation of self-emulsifying drug delivery systems. Adv Drug Deliv Rev. 1997;25(1):47-58.
-
(1997)
Adv Drug Deliv Rev.
, vol.25
, Issue.1
, pp. 47-58
-
-
Pouton, C.W.1
-
27
-
-
39149092022
-
Enhancing intestinal drug solubilisation using lipid-based delivery systems
-
Porter CJ, Pouton CW, Cuine JF, Charman WN. Enhancing intestinal drug solubilisation using lipid-based delivery systems. Adv Drug Deliv Rev. 2008;60(6):673-691
-
(2008)
Adv Drug Deliv Rev.
, vol.60
, Issue.6
, pp. 673-691
-
-
Porter, C.J.1
Pouton, C.W.2
Cuine, J.F.3
Charman, W.N.4
-
28
-
-
45849115831
-
Development of solid self-emulsifying drug delivery systems: Preparation techniques and dosage forms
-
Tang B, Cheng G, Gu JC, Xu CH. Development of solid self-emulsifying drug delivery systems: preparation techniques and dosage forms. Drug Discov Today. 2008;13(13-14):606-612
-
(2008)
Drug Discov Today.
, vol.13
, Issue.13-14
, pp. 606-612
-
-
Tang, B.1
Cheng, G.2
Gu, J.C.3
Xu, C.H.4
-
29
-
-
0034601204
-
Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs
-
Gershanik T, Benita S. Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs. Eur J Pharm Biopharm. 2000;50(1):179-188
-
(2000)
Eur J Pharm Biopharm.
, vol.50
, Issue.1
, pp. 179-188
-
-
Gershanik, T.1
Benita, S.2
-
30
-
-
33846822906
-
Microemulsions as carriers for drugs and nutraceuticals
-
Spernath A, Aserin A. Microemulsions as carriers for drugs and nutraceuticals. Adv Colloid Interface Sci. 2006;128-130:47-64.
-
(2006)
Adv Colloid Interface Sci.
, vol.128-130
, pp. 47-64
-
-
Spernath, A.1
Aserin, A.2
-
31
-
-
70449528399
-
Formulateability of ten compounds with different physicochemical profiles in SMEDDS
-
Thi TD, Van Speybroeck M, Barillaro V, Martens J, Annaert P, Augustijns P, Van Humbeeck J, Vermant J, Van den Mooter G. Formulateability of ten compounds with different physicochemical profiles in SMEDDS. Eur J Pharm Sci. 2009 Dec 8;38(5):479-488
-
(2009)
Eur J Pharm Sci.
, vol.8
, Issue.385
, pp. 479-488
-
-
Thi, T.D.1
Van Speybroeck, M.2
Barillaro, V.3
Martens, J.4
Annaert, P.5
Augustijns, P.6
Van Humbeeck, J.7
Vermant, J.8
Van Den Mooter, G.9
-
32
-
-
57449109685
-
Design and optimization of a new self-nanoemulsifying drug delivery system
-
Wang L, Dong J, Chen J, Eastoe J, Li X. Design and optimization of a new self-nanoemulsifying drug delivery system. J Colloid Interface Sci. 2009;330(2):443-448
-
(2009)
J Colloid Interface Sci.
, vol.330
, Issue.2
, pp. 443-448
-
-
Wang, L.1
Dong, J.2
Chen, J.3
Eastoe, J.4
Li, X.5
-
33
-
-
54049096692
-
Self-emulsifying drug delivery systems for improving oral absorption of ginkgo biloba extracts
-
Tang J, Sun J, Cui F, Zhang T, Liu X, He Z. Self-emulsifying drug delivery systems for improving oral absorption of ginkgo biloba extracts. Drug Deliv. 2008;15(8):477-484
-
(2008)
Drug Deliv.
, vol.15
, Issue.8
, pp. 477-484
-
-
Tang, J.1
Sun, J.2
Cui, F.3
Zhang, T.4
Liu, X.5
He, Z.6
-
34
-
-
37549031769
-
Oral bioavailability enhancement of acyclovir by self-microemulsifying drug delivery systems (SMEDDS
-
Patel D, Sawant KK. Oral bioavailability enhancement of acyclovir by self-microemulsifying drug delivery systems (SMEDDS). Drug Dev Ind Pharm. 2007;33(12):1318-1326
-
(2007)
Drug Dev Ind Pharm.
, vol.33
, Issue.12
, pp. 1318-1326
-
-
Patel, D.1
Sawant, K.K.2
-
35
-
-
0034601204
-
Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs
-
Gershanik T, Benita S. Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs. Eur J Pharm Biopharm. 2000;50(1):179-188
-
(2000)
Eur J Pharm Biopharm.
, vol.50
, Issue.1
, pp. 179-188
-
-
Gershanik, T.1
Benita, S.2
-
36
-
-
33847394968
-
Lipids and lipid-based formulations: Optimizing the oral delivery of lipophilic drugs
-
Porter CJH, Trevaskis NL, Charman WN. Lipids and lipid-based formulations: optimizing the oral delivery of lipophilic drugs. Nat Rev Drug Discov. 2007;6:231-248
-
(2007)
Nat Rev Drug Discov.
, vol.6
, pp. 231-248
-
-
Porter, C.J.H.1
Trevaskis, N.L.2
Charman, W.N.3
-
37
-
-
39149124830
-
Lipid excipients and delivery systems for pharmaceutical development: A regulatory perspective
-
Chen ML. Lipid excipients and delivery systems for pharmaceutical development: A regulatory perspective. Adv Drug Deliv Rev. 2008;60(6):768-777
-
(2008)
Adv Drug Deliv Rev.
, vol.60
, Issue.6
, pp. 768-777
-
-
Chen, M.L.1
-
38
-
-
84875438226
-
-
AHFS Drug Information. Bethesda, MD
-
McEvoy GK, Snow EK, Miller J, Kester L, Welsh OH. AHFS Drug Information. Bethesda, MD: American Society of Health-System Pharmacists, 2009.
-
(2009)
American Society of Health-System Pharmacists
-
-
McEvoy, G.K.1
Snow, E.K.2
Miller, J.3
Kester, L.4
-
40
-
-
0004074875
-
-
Sweetman SC 36th ed. London: Pharmaceutical Press
-
Sweetman SC, ed. Martindale: the complete drug reference. 36th ed. London: Pharmaceutical Press, 2009.
-
(2009)
Martindale: The Complete Drug Reference
-
-
-
41
-
-
33751014029
-
Formulation of poorly water-soluble drugs for oral administration: Physicochemical and physiological issues and the lipid formulation classification system
-
Pouton CW. Formulation of poorly water-soluble drugs for oral administration: Physicochemical and physiological issues and the lipid formulation classification system. Eur J Pharm Sci. 2006;29(3-4): 278-287
-
(2006)
Eur J Pharm Sci.
, vol.29
, Issue.3-4
, pp. 278-287
-
-
Pouton, C.W.1
-
42
-
-
34248152851
-
Self-emulsifying drug delivery systems: Strategy for improving oral delivery of poorly soluble drugs
-
Tang JL, Sun J, He ZG. Self-emulsifying drug delivery systems: strategy for improving oral delivery of poorly soluble drugs. Curr Drug Ther. 2007;2:85-93.
-
(2007)
Curr Drug Ther.
, vol.2
, pp. 85-93
-
-
Tang, J.L.1
Sun, J.2
He, Z.G.3
-
43
-
-
34848863347
-
Clinical studies with oral lipid based formulations of poorly soluble compounds
-
Fatouros DG, Karpf DM, Nielsen FS, Mullertz A. Clinical studies with oral lipid based formulations of poorly soluble compounds. Ther Clin Risk Manag. 2007;3(4):591-604.
-
(2007)
Ther Clin Risk Manag.
, vol.3
, Issue.4
, pp. 591-604
-
-
Fatouros, D.G.1
Karpf, D.M.2
Nielsen, F.S.3
Mullertz, A.4
-
44
-
-
34548049221
-
Oral lipid-based formulations
-
Hauss DJ. Oral lipid-based formulations. Adv Drug Deliv Rev. 2007 Jul 30;59(7):667-676
-
(2007)
Adv Drug Deliv Rev
, vol.30
, Issue.59
, pp. 667-676
-
-
Hauss, D.J.1
-
45
-
-
0029562489
-
Lipid microemulsions for improving drug dissolution and oral absorption: Physical and biopharmaceutical aspects
-
Constantinides PP. Lipid microemulsions for improving drug dissolution and oral absorption: physical and biopharmaceutical aspects. Pharm Res. 1995;12(11):1561-1572
-
(1995)
Pharm Res.
, vol.12
, Issue.11
, pp. 1561-1572
-
-
Constantinides1
-
46
-
-
24644482608
-
Interest of multifunctional lipid excipients: Case of Gelucire 44/14
-
Chambin O, Jannin V. Interest of multifunctional lipid excipients: case of Gelucire 44/14. Drug Dev Ind Pharm. 2005;31(6):527-534
-
(2005)
Drug Dev Ind Pharm.
, vol.31
, Issue.6
, pp. 527-534
-
-
Chambin, O.1
Jannin, V.2
-
47
-
-
0031914282
-
Lipid-based delivery systems for improving the bioavailability and lymphatic transport of a poorly water-soluble LTB4 inhibitor
-
Hauss DJ, Fogal SE, Ficorilli JV, Price CA, Roy T, Jayaraj AA, Keirns JJ. Lipid-based delivery systems for improving the bioavailability and lymphatic transport of a poorly water-soluble LTB4 inhibitor. J Pharm Sci. 1998;87(2):164-169
-
(1998)
J Pharm Sci.
, vol.87
, Issue.2
, pp. 164-169
-
-
Hauss, D.J.1
Fogal, S.E.2
Ficorilli, J.V.3
Price, C.A.4
Roy, T.5
Jayaraj, A.A.6
Keirns, J.J.7
-
48
-
-
34548049221
-
Oral lipid-based formulations
-
Hauss DJ. Oral lipid-based formulations. Adv Drug Deliv Rev. 2007;59(7):667-676
-
(2007)
Adv Drug Deliv Rev.
, vol.59
, Issue.7
, pp. 667-676
-
-
Hauss, D.J.1
-
49
-
-
0343418424
-
A study of self-emulsifying oil/surfactant mixtures [PhD thesis]
-
Pouton CW. A study of self-emulsifying oil/surfactant mixtures [PhD thesis]. London: University of London, 1982.
-
(1982)
London: University of London
-
-
Pouton, C.W.1
-
50
-
-
1642376495
-
The emulsification and solubilisation properties of polyglycolysed oils in self-emulsifying formulations
-
Devani M, Ashford M, Craig DQ. The emulsification and solubilisation properties of polyglycolysed oils in self-emulsifying formulations. J Pharm Pharmacol. 2004;56(3):307-316
-
(2004)
J Pharm Pharmacol.
, vol.56
, Issue.3
, pp. 307-316
-
-
Devani, M.1
Ashford, M.2
Craig, D.Q.3
-
51
-
-
0022366625
-
Self-emulsifying drug delivery systems: Assessment of the efficiency of emulsification
-
Pouton CW. Self-emulsifying drug delivery systems: assessment of the efficiency of emulsification. Int J Pharm. 1985;27(2-3):335-348
-
(1985)
Int J Pharm.
, vol.27
, Issue.2-3
, pp. 335-348
-
-
Pouton, C.W.1
-
52
-
-
0024218073
-
Effect of vehicle amphiphilicity on the dissolution and bioavailability of a poorly water-soluble drug from solid dispersions
-
Serajuddin AT, Sheen PC, Mufson D, Bernstein DF, Augustine MA. Effect of vehicle amphiphilicity on the dissolution and bioavailability of a poorly water-soluble drug from solid dispersions. J Pharm Sci. 1988;77(5):414-417
-
(1988)
J Pharm Sci.
, vol.77
, Issue.5
, pp. 414-417
-
-
Serajuddin, A.T.1
Sheen, P.C.2
Mufson, D.3
Bernstein, D.F.4
Augustine, M.A.5
-
53
-
-
0028194817
-
Self-emulsifying drug delivery systems (SEDDS) with polyglycolyzed glycerides for improving in vitro dissolution and oral absorption of lipophilic drugs
-
Shah NH, Carvajal MT, Patel CI, Infeld MH, Malick AW. Self-emulsifying drug delivery systems (SEDDS) with polyglycolyzed glycerides for improving in vitro dissolution and oral absorption of lipophilic drugs. Int J Pharm. 1994;106(1):15-23.
-
(1994)
Int J Pharm.
, vol.106
, Issue.1
, pp. 15-23
-
-
Shah, N.H.1
Carvajal, M.T.2
Patel, C.I.3
Infeld, M.H.4
Malick, A.W.5
-
54
-
-
60749119779
-
The use of liquid selfmicroemulsifying drug delivery systems based on peanut oil/tween 80 in the delivery of griseofulvin
-
Ofokansi KC, Chukwu KI, Ugwuanyi SI. The use of liquid selfmicroemulsifying drug delivery systems based on peanut oil/tween 80 in the delivery of griseofulvin. Drug Dev Ind Pharm. 2009;35(2): 185-191
-
(2009)
Drug Dev Ind Pharm.
, vol.35
, Issue.2
, pp. 185-191
-
-
Ofokansi, K.C.1
Chukwu, K.I.2
Ugwuanyi, S.I.3
-
56
-
-
51449089455
-
Pluronic and tetronic copolymers with polyglycolyzed oils as self-emulsifying drug delivery systems
-
Fernandez-Tarrio M, Yanez F, Immesoete K, Alvarez-Lorenzo C, Concheiro A. Pluronic and tetronic copolymers with polyglycolyzed oils as self-emulsifying drug delivery systems. AAPS PharmSciTech. 2008;9(2):471-479
-
(2008)
AAPS PharmSciTech.
, vol.9
, Issue.2
, pp. 471-479
-
-
Fernandez-Tarrio, M.1
Yanez, F.2
Immesoete, K.3
Alvarez-Lorenzo, C.4
Concheiro, A.5
-
58
-
-
10644257823
-
Effect of combined use of nonionic surfactant on formation of oil-in-water microemulsions
-
Li P, Ghosh A, Wagner RF, Krill S, Joshi YM, Serajuddin ATM. Effect of combined use of nonionic surfactant on formation of oil-in-water microemulsions. Int J Pharm. 2005;288(1):27-34.
-
(2005)
Int J Pharm.
, vol.288
, Issue.1
, pp. 27-34
-
-
Li, P.1
Ghosh, A.2
Wagner, R.F.3
Krill, S.4
Joshi, Y.M.5
Serajuddin, A.T.M.6
-
59
-
-
50449093858
-
Intestinal lymphatic transport of halofantrine in rats assessed using a chylomicron flow blocking approach: The influence of polysorbate 60 and 80
-
Lind ML, Jacobsen J, Holm R, Mullertz A. Intestinal lymphatic transport of halofantrine in rats assessed using a chylomicron flow blocking approach: the influence of polysorbate 60 and 80. Eur J Pharm Sci. 2008;35(3):211-218
-
(2008)
Eur J Pharm Sci.
, vol.35
, Issue.3
, pp. 211-218
-
-
Lind, M.L.1
Jacobsen, J.2
Holm, R.3
Mullertz, A.4
-
60
-
-
0032764767
-
Spontaneous emulsification of oils containing hydrocarbon, nonionic surfactant, and oleyl alcohol
-
Rang MJ, Miller CA. Spontaneous emulsification of oils containing hydrocarbon, nonionic surfactant, and oleyl alcohol. J Colloid Interface Sci. 1999;209(1):179-192
-
(1999)
J Colloid Interface Sci.
, vol.209
, Issue.1
, pp. 179-192
-
-
Rang, M.J.1
Miller, C.A.2
-
61
-
-
43249122851
-
Bioavailability of probucol from lipid and surfactant based formulations in minipigs: Influence of droplet size and dietary state
-
Nielsen FS, Petersen KB, Müllertz A. Bioavailability of probucol from lipid and surfactant based formulations in minipigs: Influence of droplet size and dietary state. Eur J Pharm Biopharm. 2008;69(2):553-562
-
(2008)
Eur J Pharm Biopharm.
, vol.69
, Issue.2
, pp. 553-562
-
-
Nielsen, F.S.1
Petersen, K.B.2
Müllertz, A.3
-
62
-
-
3543106201
-
Influence of lipolysis and droplet size on tocotrienol absorption from self-emulsifying formulations
-
Yap SP, Yuen KH. Influence of lipolysis and droplet size on tocotrienol absorption from self-emulsifying formulations. Int J Pharm. 2004;281(1-2):67-78.
-
(2004)
Int J Pharm.
, vol.281
, Issue.1-2
, pp. 67-78
-
-
Yap, S.P.1
Yuen, K.H.2
-
63
-
-
0031780652
-
Interaction of a self-emulsifying lipid drug delivery system with the everted rat intestinal mucosa as a function of droplet size and surface charge
-
Gershanik T, Benzeno S, Benita S. Interaction of a self-emulsifying lipid drug delivery system with the everted rat intestinal mucosa as a function of droplet size and surface charge. Pharm Res. 1998;15(6): 863-869
-
(1998)
Pharm Res.
, vol.15
, Issue.6
, pp. 863-869
-
-
Gershanik, T.1
Benzeno, S.2
Benita, S.3
-
64
-
-
0028949717
-
An investigation into the mechanisms of self-emulsification using particle size analysis and low frequency dielectric spectroscopy
-
Craig DQM, Barker SA, Banning D, Booth SW. An investigation into the mechanisms of self-emulsification using particle size analysis and low frequency dielectric spectroscopy. Int J Pharm. 1995;114(1):103-110
-
(1995)
Int J Pharm.
, vol.114
, Issue.1
, pp. 103-110
-
-
Craig, D.Q.M.1
Barker, S.A.2
Banning, D.3
Booth, S.W.4
-
65
-
-
0035895309
-
Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10: Formulation development and bioavailability assessment
-
Kommuru TR, Gurley B, Khan MA, Reddy IK. Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10: formulation development and bioavailability assessment. Int J Pharm. 2001;212(2):233-246
-
(2001)
Int J Pharm.
, vol.212
, Issue.2
, pp. 233-246
-
-
Kommuru, T.R.1
Gurley, B.2
Khan, M.A.3
Reddy, I.K.4
-
66
-
-
0028000096
-
Rationale for the development of Sandimmune Neoral
-
Vonderscher J, Meinzer A. Rationale for the development of Sandimmune Neoral. Transplant Proc. 1994;26(5):2925-2927
-
(1994)
Transplant Proc.
, vol.26
, Issue.5
, pp. 2925-2927
-
-
Vonderscher, J.1
Meinzer, A.2
-
67
-
-
44849119532
-
Design and evaluation of self-emulsifying drug delivery systems (SEDDS) of nimodipine
-
Kale AA, Patravale VB. Design and evaluation of self-emulsifying drug delivery systems (SEDDS) of nimodipine. AAPS PharmSciTech. 2008;9(1):191-196
-
(2008)
AAPS PharmSciTech.
, vol.9
, Issue.1
, pp. 191-196
-
-
Kale, A.A.1
Patravale, V.B.2
-
68
-
-
67049096635
-
Development and characterization of self-microemulsifying drug delivery system of tacrolimus for intravenous administration
-
Borhade VB, Nair HA, Hegde DD. Development and characterization of self-microemulsifying drug delivery system of tacrolimus for intravenous administration. Drug Dev Ind Pharm. 2009;35(5):619-630
-
(2009)
Drug Dev Ind Pharm.
, vol.35
, Issue.5
, pp. 619-630
-
-
Borhade, V.B.1
Nair, H.A.2
Hegde, D.D.3
-
69
-
-
0011379669
-
Entropy-induced dispersion of bulk liquids
-
Reiss H. Entropy-induced dispersion of bulk liquids. J Colloid Interface Sci. 1975;53(1):61-70.
-
(1975)
J Colloid Interface Sci.
, vol.53
, Issue.1
, pp. 61-70
-
-
Reiss, H.1
-
70
-
-
0037139412
-
Preparation and in vitro characterization of a eutectic based semisolid self-nanoemulsified drug delivery system (SNEDDS) of ubiquinone: Mechanism and progress of emulsion formation
-
Nazzal S, Smalyukh II, Lavrentovich OD, Khan MA. Preparation and in vitro characterization of a eutectic based semisolid self-nanoemulsified drug delivery system (SNEDDS) of ubiquinone: mechanism and progress of emulsion formation. Int J Pharm. 2002;235(1-2):247-265
-
(2002)
Int J Pharm.
, vol.235
, Issue.1-2
, pp. 247-265
-
-
Nazzal, S.1
Smalyukh, I.I.2
Lavrentovich, O.D.3
Khan, M.A.4
-
71
-
-
0033080454
-
Emulsification through area contraction
-
Dabros T, Yeung A, Masliyah J, Czarnecki J. Emulsification through area contraction. J Colloid Interface Sci. 1999;210(1):222-224
-
(1999)
J Colloid Interface Sci.
, vol.210
, Issue.1
, pp. 222-224
-
-
Dabros, T.1
Yeung, A.2
Masliyah, J.3
Czarnecki, J.4
-
72
-
-
0027301116
-
An investigation into the physico-chemical properties of self-emulsifying systems using low frequency dielectric spectroscopy, surface tension measurements and particle size analysis
-
Craig DQM, Lievens HSR, Pitt KG, Storey DE. An investigation into the physico-chemical properties of self-emulsifying systems using low frequency dielectric spectroscopy, surface tension measurements and particle size analysis. Int J Pharm. 1993;96(1-3):147-155
-
(1993)
Int J Pharm.
, vol.96
, Issue.1-3
, pp. 147-155
-
-
Craig, D.Q.M.1
Lievens, H.S.R.2
Pitt, K.G.3
Storey, D.E.4
-
73
-
-
0344944850
-
Spontaneous formation of lipid structures at oil/water/lipid interfaces
-
Pautot S, Frisken BJ, Cheng J-X, Xie XS, Weitz DA. Spontaneous formation of lipid structures at oil/water/lipid interfaces. Langmuir. 2003;19 (24):10281-10287
-
(2003)
Langmuir.
, vol.19
, Issue.24
, pp. 10281-10287
-
-
Pautot, S.1
Frisken, B.J.2
Cheng, J.-X.3
Xie, X.S.4
Weitz, D.A.5
-
74
-
-
30344456981
-
Development of supersaturatable self-emulsifying drug delivery system formulations for improving the oral absorption of poorly soluble drugs
-
Gao P, Morozowich W. Development of supersaturatable self-emulsifying drug delivery system formulations for improving the oral absorption of poorly soluble drugs. Expert Opin Drug Deliv. 2006;3(1):97-110.
-
(2006)
Expert Opin Drug Deliv.
, vol.3
, Issue.1
, pp. 97-110
-
-
Gao, P.1
Morozowich, W.2
-
75
-
-
0344012523
-
Development of a supersaturable SEDDS (S-SEDDS) formulation of paclitaxel with improved oral bioavailability
-
Gao P, Rush BD, Pfund WP, Huang T, Bauer JM, Morozowich W, Kuo MS, Hageman MJ. Development of a supersaturable SEDDS (S-SEDDS) formulation of paclitaxel with improved oral bioavailability. J Pharm Sci. 2003;92(12):2386- 2398
-
(2003)
J Pharm Sci.
, vol.92
, Issue.12
, pp. 2386-2398
-
-
Gao, P.1
Rush, B.D.2
Pfund, W.P.3
Huang, T.4
Bauer, J.M.5
Morozowich, W.6
Kuo, M.S.7
Hageman, M.J.8
-
76
-
-
0025727540
-
Intestinal absorption of drugs: The influence of mixed micelles on on the disappearance kinetics of drugs from the small intestine of the rat
-
Poelma FG, Breas R, Tukker JJ, Crommelin DJ. Intestinal absorption of drugs: the influence of mixed micelles on on the disappearance kinetics of drugs from the small intestine of the rat. J Pharm Pharmacol. 1991;43(5):317-324
-
(1991)
J Pharm Pharmacol.
, vol.43
, Issue.5
, pp. 317-324
-
-
Poelma, F.G.1
Breas, R.2
Tukker, J.J.3
Crommelin, D.J.4
-
77
-
-
1842589355
-
Enhanced oral bioavailability of a poorly water soluble drug PNU-91325 by supersaturatable formulations
-
Gao P, Guyton ME, Huang T, Bauer JM, Stefanski KJ, Lu Q. Enhanced oral bioavailability of a poorly water soluble drug PNU-91325 by supersaturatable formulations. Drug Dev Ind Pharm. 2004;30(2):221-229
-
(2004)
Drug Dev Ind Pharm.
, vol.30
, Issue.2
, pp. 221-229
-
-
Gao, P.1
Guyton, M.E.2
Huang, T.3
Bauer, J.M.4
Stefanski, K.J.5
Lu, Q.6
-
78
-
-
44649133855
-
Rationalizing the selection of oral lipid based drug delivery systems by an in vitro dynamic lipolysis model for improved oral bioavailability of poorly water soluble drugs
-
Dahan A, Hoffman A. Rationalizing the selection of oral lipid based drug delivery systems by an in vitro dynamic lipolysis model for improved oral bioavailability of poorly water soluble drugs. J Control Release. 2008;129(1):1-10.
-
(2008)
J Control Release.
, vol.129
, Issue.1
, pp. 1-10
-
-
Dahan, A.1
Hoffman, A.2
-
79
-
-
55749086418
-
Speeding the development of poorly soluble/poorly permeable drugs by SEDDS/S-SEDDS formulations and prodrugs, Part 1
-
Morozowich W, Gao P, Charton M. Speeding the development of poorly soluble/poorly permeable drugs by SEDDS/S-SEDDS formulations and prodrugs, Part 1. Am Pharm Rev. 2006;9:110-114
-
(2006)
Am Pharm Rev.
, vol.9
, pp. 110-114
-
-
Morozowich, W.1
Gao, P.2
-
80
-
-
55749086418
-
Speeding the development of poorly soluble/poorly permeable drugs by SEDDS/S-SEDDS formulations and prodrugs, Part 2
-
Gao P, Charton M, Morozowich W. Speeding the development of poorly soluble/poorly permeable drugs by SEDDS/S-SEDDS formulations and prodrugs, Part 2. Am Pharm Rev. 2006;9:16-23.
-
(2006)
Am Pharm Rev.
, vol.9
, pp. 16-23
-
-
Gao, P.1
Charton, M.2
Morozowich, W.3
-
81
-
-
0027956965
-
Effect of supersaturation on membrane transport
-
Pellett MA, Davis AF, Hadgraft J. Effect of supersaturation on membrane transport: 2. Piroxicam. Int J Pharm. 1994;111(1):1-6.
-
(1994)
Int J Pharm.
, vol.2
, Issue.111
, pp. 1-6
-
-
Pellett, M.A.1
Davis, A.F.2
Hadgraft, J.3
-
82
-
-
0030920786
-
Supersaturated solutions evaluated with an in vitro stratum corneum tape stripping technique
-
Pellett MA, Roberts MS, Hadgraft J. Supersaturated solutions evaluated with an in vitro stratum corneum tape stripping technique. Int J Pharm. 1997;151(1):91-98
-
(1997)
Int J Pharm.
, vol.151
, Issue.1
, pp. 91-98
-
-
Pellett, M.A.1
Roberts, M.S.2
Hadgraft, J.3
-
83
-
-
0033986929
-
Effect of cellulose polymers on supersaturation and in vitro membrane transport of hydrocortisone acetate
-
Raghavan SL, Trividic A, Davis AF, Hadgraft J. Effect of cellulose polymers on supersaturation and in vitro membrane transport of hydrocortisone acetate. Int J Pharm. 2000;193(2):231-237
-
(2000)
Int J Pharm.
, vol.193
, Issue.2
, pp. 231-237
-
-
Raghavan, S.L.1
Trividic, A.2
Davis, A.F.3
Hadgraft, J.4
-
84
-
-
48149088784
-
Self-microemulsifying drug delivery system (SMEDDS) improves anticancer effect of oral 9-nitrocamptothecin on human cancer xenografts in nude mice
-
Lu J-L, Wang J-C, Zhao S-X, Liu X-Y, Zhao H, Zhang X, Zhou S-F, Zhang Q. Self-microemulsifying drug delivery system (SMEDDS) improves anticancer effect of oral 9-nitrocamptothecin on human cancer xenografts in nude mice. Eur J Pharm Biopharm. 2008;69(3):899-907.
-
(2008)
Eur J Pharm Biopharm.
, vol.69
, Issue.3
, pp. 899-907
-
-
Lu, J.-L.1
Wang, J.-C.2
Zhao, S.-X.3
Liu, X.-Y.4
Zhao, H.5
Zhang, X.6
Zhou, S.-F.7
Zhang, Q.8
-
85
-
-
5444247353
-
Preparation and in vitro characterization of self-nanoemulsified drug delivery system (SNEDDS) of all-trans-retinol acetate
-
Taha EI, Al-Saidan S, Samy AM, Khan MA. Preparation and in vitro characterization of self-nanoemulsified drug delivery system (SNEDDS) of all-trans-retinol acetate. Int J Pharm. 2004;285(1-2):109-119
-
(2004)
Int J Pharm.
, vol.285
, Issue.1-2
, pp. 109-119
-
-
Taha, E.I.1
Al-Saidan, S.2
Samy, A.M.3
Khan, M.A.4
-
86
-
-
33847247476
-
Development of self-microemulsifying drug delivery systems for oral bioavailability enhancement of alpha-Asarone in beagle dogs
-
Wang DK, Shi ZH, Liu L, Wang XY, Zhang CX, Zhao P. Development of self-microemulsifying drug delivery systems for oral bioavailability enhancement of alpha-Asarone in beagle dogs. PDA J Pharm Sci Technol. 2006;60(6):343-349
-
(2006)
PDA J Pharm Sci Technol.
, vol.60
, Issue.6
, pp. 343-349
-
-
Wang, D.K.1
Shi, Z.H.2
Liu, L.3
Wang, X.Y.4
Zhang, C.X.5
Zhao, P.6
-
87
-
-
64149117052
-
Development and characterization of oral lipid-based Amphotericin B formulations with enhanced drug solubility, stability and antifungal activity in rats infected with Aspergillus fumigatus or Candida albicans
-
Wasan EK, Bartlett K, Gershkovich P, Sivak O, Banno B, Wong Z, Gagnon J, Gates B, Leon CG, Wasan KM. Development and characterization of oral lipid-based Amphotericin B formulations with enhanced drug solubility, stability and antifungal activity in rats infected with Aspergillus fumigatus or Candida albicans. Int J Pharm. 2009;372(1-2):76-84.
-
(2009)
Int J Pharm.
, vol.372
, Issue.1-2
, pp. 76-84
-
-
Wasan, E.K.1
Bartlett, K.2
Gershkovich, P.3
Sivak, O.4
Banno, B.5
Wong, Z.6
Gagnon, J.7
Gates, B.8
Leon, C.G.9
Wasan, K.M.10
-
88
-
-
33748290093
-
Preparation and evaluation of self-microemulsifying drug delivery systems (SMEDDS) containing atorvastatin
-
Shen H, Zhong M. Preparation and evaluation of self-microemulsifying drug delivery systems (SMEDDS) containing atorvastatin. J Pharm Pharmacol. 2006;58(9):1183-1191
-
(2006)
J Pharm Pharmacol.
, vol.58
, Issue.9
, pp. 1183-1191
-
-
Shen, H.1
Zhong, M.2
-
89
-
-
23944475628
-
Enhancement of the stability of BCNU using self-emulsifying drug delivery systems (SEDDS) and in vitro antitumor activity of self-emulsified BCNU-loaded PLGA wafer
-
Chae GS, Lee JS, Kim SH, Seo KS, Kim MS, Lee HB, Khang G. Enhancement of the stability of BCNU using self-emulsifying drug delivery systems (SEDDS) and in vitro antitumor activity of self-emulsified BCNU-loaded PLGA wafer. Int J Pharm. 2005;301(1-2):6-14.
-
(2005)
Int J Pharm.
, vol.301
, Issue.1-2
, pp. 6-14
-
-
Chae, G.S.1
Lee, J.S.2
Kim, S.H.3
Seo, K.S.4
Kim, M.S.5
Lee, H.B.6
Khang, G.7
-
90
-
-
50249132541
-
Self-nanoemulsifying drug delivery systems (SNEDDS) for oral delivery of protein drugs
-
Rao SV, Shao J. Self-nanoemulsifying drug delivery systems (SNEDDS) for oral delivery of protein drugs: I. Formulation development. Int J Pharm. 2008;362(1-2):2-9.
-
(2008)
Int J Pharm.
, vol.1
, Issue.362
, pp. 2-9
-
-
Rao, S.V.1
Shao, J.2
-
91
-
-
50249090401
-
Self-nanoemulsifying drug delivery systems (SNEDDS) for oral delivery of protein drugs: II
-
Rao SVR, Agarwal P, Shao J. Self-nanoemulsifying drug delivery systems (SNEDDS) for oral delivery of protein drugs: II. In vitro transport study. Int J Pharm. 2008;362(1-2):10-15
-
(2008)
In Vitro Transport Study. Int J Pharm.
, vol.362
, Issue.1-2
, pp. 10-15
-
-
Rao, S.V.R.1
Agarwal, P.2
Shao, J.3
-
92
-
-
25144440877
-
Preparation and evaluation of SEDDS and SMEDDS containing carvedilol
-
Wei L, Sun P, Nie S, Pan W. Preparation and evaluation of SEDDS and SMEDDS containing carvedilol. Drug Dev Ind Pharm. 2005;31(8):785-794
-
(2005)
Drug Dev Ind Pharm.
, vol.31
, Issue.8
, pp. 785-794
-
-
Wei, L.1
Sun, P.2
Nie, S.3
Pan, W.4
-
93
-
-
76849110818
-
Self nano emulsifying drug delivery systems (snedds) of carvedilol: Design, optimization, characterization and evaluation
-
College of Pharmacy, Moga, Punjab, India, October
-
Singh B, Singh R, Bandyopadhyay S, Mohapatra A. Self nano emulsifying drug delivery systems (snedds) of carvedilol: design, optimization, characterization and evaluation. Proceedings of the AICTE-Sponsored National Conference on Nano-Colloidal Carrier: Site Specific & Controlled Drug Delivery, I.S.F. College of Pharmacy, Moga, Punjab, India, October 10-11, 2008.
-
(2008)
Proceedings of the AICTE-Sponsored National Conference on Nano-Colloidal Carrier: Site Specific & Controlled Drug Delivery, I.S.F
, pp. 10-11
-
-
Singh, B.1
Singh, R.2
Bandyopadhyay, S.3
Mohapatra, A.4
-
94
-
-
67549143093
-
Preparation and evaluation of self-nanoemulsifying tablets of carvedilol
-
Mahmoud EA, Bendas ER, Mohamed MI. Preparation and evaluation of self-nanoemulsifying tablets of carvedilol. AAPS PharmSciTech. 2009;10(1):183-192
-
(2009)
AAPS PharmSciTech.
, vol.10
, Issue.1
, pp. 183-192
-
-
Mahmoud, E.A.1
Bendas, E.R.2
Mohamed, M.I.3
-
95
-
-
34347376910
-
Application of a statistical method to the absorption of a new model drug from micellar and lipid formulations--evaluation of qualitative excipient effects
-
Kuentz M, Wyttenbach N, Kuhlmann O. Application of a statistical method to the absorption of a new model drug from micellar and lipid formulations--evaluation of qualitative excipient effects. Pharm Dev Technol. 2007;12(3):275-283
-
(2007)
Pharm Dev Technol.
, vol.12
, Issue.3
, pp. 275-283
-
-
Kuentz, M.1
Wyttenbach, N.2
Kuhlmann, O.3
-
96
-
-
33845576641
-
Design and evaluation of self-nanoemulsifying drug delivery systems (SNEDDS) for cefpodoxime proxetil
-
Date AA, Nagarsenker MS. Design and evaluation of self-nanoemulsifying drug delivery systems (SNEDDS) for cefpodoxime proxetil. Int J Pharm. 2007;329(1-2):166-172
-
(2007)
Int J Pharm.
, vol.329
, Issue.1-2
, pp. 166-172
-
-
Date, A.A.1
Nagarsenker, M.S.2
-
97
-
-
21644461482
-
Formulation design of self-microemulsifying drug delivery systems for improved oral bioavailability of celecoxib
-
Subramanian N, Ray S, Ghosal SK, Bhadra R, Moulik SP. Formulation design of self-microemulsifying drug delivery systems for improved oral bioavailability of celecoxib. Biol Pharm Bull. 2004;27(12):1993-1999
-
(2004)
Biol Pharm Bull.
, vol.27
, Issue.12
, pp. 1993-1999
-
-
Subramanian, N.1
Ray, S.2
Ghosal, S.K.3
Bhadra, R.4
Moulik, S.P.5
-
98
-
-
1542358756
-
Evaluation of cytotoxicity of oils used in coenzyme Q10 self-emulsifying drug delivery systems (SEDDS
-
Palamakula A, Khan MA. Evaluation of cytotoxicity of oils used in coenzyme Q10 self-emulsifying drug delivery systems (SEDDS). Int J Pharm. 2004;273(1-2):63-73.
-
(2004)
Int J Pharm.
, vol.273
, Issue.1-2
, pp. 63-73
-
-
Palamakula, A.1
Khan, M.A.2
-
99
-
-
67349166936
-
Enhanced oral bioavailability of coenzyme Q10 by self-emulsifying drug delivery systems
-
Balakrishnan P, Lee BJ, Oh DH, Kim JO, Lee YI, Kim DD, Jee JP, Lee YB, Woo JS, Yong CS, Choi HG. Enhanced oral bioavailability of coenzyme Q10 by self-emulsifying drug delivery systems. Int J Pharm. 2009;374(1-2):66-72.
-
(2009)
Int J Pharm.
, vol.374
, Issue.1-2
, pp. 66-72
-
-
Balakrishnan, P.1
Lee, B.J.2
Oh, D.H.3
Kim, J.O.4
Lee, Y.I.5
Kim, D.D.6
Jee, J.P.7
Lee, Y.B.8
Woo, J.S.9
Yong, C.S.10
Choi, H.G.11
-
100
-
-
73449127250
-
Self-microemulsifying formulationbased oral solution of coenzyme Q10
-
Seo DW, Kang MJ, Sohn Y, Lee J. Self-microemulsifying formulationbased oral solution of coenzyme Q10. Yakugaku Zasshi. 2009;129(12):1559-1563
-
(2009)
Yakugaku Zasshi.
, vol.129
, Issue.12
, pp. 1559-1563
-
-
Seo, D.W.1
Kang, M.J.2
Sohn, Y.3
Lee, J.4
-
101
-
-
33846852628
-
Quality by design: Understanding the formulation variables of a cyclosporine A self-nanoemulsified drug delivery systems by BoxBehnken design and desirability function
-
Zidan AS, Sammour OA, Hammad MA, Megrab NA, Habib MJ, Khan MA. Quality by design: understanding the formulation variables of a cyclosporine A self-nanoemulsified drug delivery systems by BoxBehnken design and desirability function. Int J Pharm. 2007;332(1- 2):55-63.
-
(2007)
Int J Pharm.
, vol.332
, Issue.1-2
, pp. 55-63
-
-
Zidan, A.S.1
Sammour, O.A.2
Hammad, M.A.3
Megrab, N.A.4
Habib, M.J.5
Khan, M.A.6
-
102
-
-
0344514705
-
Lipid drug delivery and rational formulation design for lipophilic drugs with low oral bioavailability, applied to cyclosporine
-
Odeberg JM, Kaufmann P, Kroon KG, Hoglund P. Lipid drug delivery and rational formulation design for lipophilic drugs with low oral bioavailability, applied to cyclosporine. Eur J Pharm Sci. 2003;20(4-5):375-382
-
(2003)
Eur J Pharm Sci.
, vol.20
, Issue.4-5
, pp. 375-382
-
-
Odeberg, J.M.1
Kaufmann, P.2
Kroon, K.G.3
Hoglund, P.4
-
103
-
-
75549090471
-
Porous magnesium aluminometasilicate tablets as carrier of a cyclosporine self-emulsifying formulation
-
Nov 20. [Epub ahead of print]
-
Sander C, Holm P. Porous magnesium aluminometasilicate tablets as carrier of a cyclosporine self-emulsifying formulation. AAPS PharmSciTech. 2009 Nov 20. [Epub ahead of print]
-
(2009)
AAPS PharmSciTech.
-
-
Sander, C.1
Holm, P.2
-
104
-
-
33847364354
-
Increasing the proportional content of surfactant (Cremophor EL) relative to lipid in self-emulsifying lipid-based formulations of danazol reduces oral bioavailability in beagle dogs
-
Cuine JF, Charman WN, Pouton CW, Edwards GA, Porter CJ. Increasing the proportional content of surfactant (Cremophor EL) relative to lipid in self-emulsifying lipid-based formulations of danazol reduces oral bioavailability in beagle dogs. Pharm Res. 2007;24(4):748-757
-
(2007)
Pharm Res.
, vol.24
, Issue.4
, pp. 748-757
-
-
Cuine, J.F.1
Charman, W.N.2
Pouton, C.W.3
Edwards, G.A.4
Porter, C.J.5
-
105
-
-
34247472175
-
Characterization of prototype self-nanoemulsifying formulations of lipophilic compounds
-
Nielsen FS, Gibault E, Ljusberg-Wahren H, Arleth L, Pedersen JS, Mullertz A. Characterization of prototype self-nanoemulsifying formulations of lipophilic compounds. J Pharm Sci. 2007;96(4):876-892
-
(2007)
J Pharm Sci.
, vol.96
, Issue.4
, pp. 876-892
-
-
Nielsen, F.S.1
Gibault, E.2
Ljusberg-Wahren, H.3
Arleth, L.4
Pedersen, J.S.5
Mullertz, A.6
-
106
-
-
47149099427
-
Self-nanoemulsifying drug delivery system for enhanced bioavailability and improved hepatoprotective activity of biphenyl dimethyl dicarboxylate
-
El-Laithy HM. Self-nanoemulsifying drug delivery system for enhanced bioavailability and improved hepatoprotective activity of biphenyl dimethyl dicarboxylate. Curr Drug Deliv. 2008;5(3):170-176
-
(2008)
Curr Drug Deliv.
, vol.5
, Issue.3
, pp. 170-176
-
-
El-Laithy, H.M.1
-
107
-
-
67449116319
-
Enhanced oral bioavailability of dexibuprofen by a novel solid self-emulsifying drug delivery system (SEDDS
-
Balakrishnan P, Lee BJ, Oh DH, Kim JO, Hong MJ, Jee JP, Kim JA, Yoo BK, Woo JS, Yong CS, Choi HG. Enhanced oral bioavailability of dexibuprofen by a novel solid self-emulsifying drug delivery system (SEDDS). Eur J Pharm Biopharm. 2009;72(3):539-545
-
(2009)
Eur J Pharm Biopharm.
, vol.72
, Issue.3
, pp. 539-545
-
-
Balakrishnan, P.1
Lee, B.J.2
Oh, D.H.3
Kim, J.O.4
Hong, M.J.5
Jee, J.P.6
Kim, J.A.7
Yoo, B.K.8
Woo, J.S.9
Yong, C.S.10
Choi, H.G.11
-
108
-
-
34247536269
-
Preparation and characterization of a self-emulsifying pellet formulation
-
Abdalla A, Mader K. Preparation and characterization of a self-emulsifying pellet formulation. Eur J Pharm Biopharm. 2007;66(2):220-226
-
(2007)
Eur J Pharm Biopharm.
, vol.66
, Issue.2
, pp. 220-226
-
-
Abdalla, A.1
Mader, K.2
-
109
-
-
0042634183
-
The use of solid self-emulsifying systems in the delivery of diclofenac
-
Attama AA, Nzekwe IT, Nnamani PO, Adikwu MU, Onugu CO. The use of solid self-emulsifying systems in the delivery of diclofenac. Int J Pharm. 2003;262(1-2):23-28
-
(2003)
Int J Pharm.
, vol.262
, Issue.1-2
, pp. 23-28
-
-
Attama, A.A.1
Nzekwe, I.T.2
Nnamani, P.O.3
Adikwu, M.U.4
Onugu, C.O.5
-
110
-
-
67549127535
-
Extended release felodipine selfnanoemulsifying system
-
Patil PR, Biradar SV, Paradkar AR. Extended release felodipine selfnanoemulsifying system. AAPS PharmSciTech. 2009;10(2):515-523
-
(2009)
AAPS PharmSciTech.
, vol.10
, Issue.2
, pp. 515-523
-
-
Patil, P.R.1
Biradar, S.V.2
Paradkar, A.R.3
-
111
-
-
38849151208
-
Preparation and in vivo evaluation of SMEDDS (self-microemulsifying drug delivery system) containing fenofibrate
-
Patel AR, Vavia PR. Preparation and in vivo evaluation of SMEDDS (self-microemulsifying drug delivery system) containing fenofibrate. AAPS J. 2007;9(3):E344-52.
-
(2007)
AAPS J.
, vol.9
, Issue.3
-
-
Patel, A.R.1
Vavia, P.R.2
-
112
-
-
70349238697
-
Design of lipid-based formulations for oral administration of poorly water-soluble drugs: Precipitation of drug after dispersion of formulations in aqueous solution
-
Mohsin K, Long MA, Pouton CW. Design of lipid-based formulations for oral administration of poorly water-soluble drugs: precipitation of drug after dispersion of formulations in aqueous solution. J Pharm Sci. 2009;98(10):3582-3595
-
(2009)
J Pharm Sci.
, vol.98
, Issue.10
, pp. 3582-3595
-
-
Mohsin, K.1
Long, M.A.2
Pouton, C.W.3
-
113
-
-
70049093306
-
Preparation of the oral selfmicroemulsifying drug delivery system of GBE50
-
Xiong Y, Liu QD, Lai L, Chen JH. Preparation of the oral selfmicroemulsifying drug delivery system of GBE50. Yao Xue Xue Bao. 2009;44(7):803-808
-
(2009)
Yao Xue Xue Bao.
, vol.44
, Issue.7
, pp. 803-808
-
-
Xiong, Y.1
Liu, Q.D.2
Lai, L.3
Chen, J.H.4
-
114
-
-
20444508016
-
Oral solid gentamicin preparation using emulsifier and adsorbent
-
Ito Y, Kusawake T, Ishida M, Tawa R, Shibata N, Takada K. Oral solid gentamicin preparation using emulsifier and adsorbent. J Control Release. 2005;105(1-2):23-31.
-
(2005)
J Control Release.
, vol.105
, Issue.1-2
, pp. 23-31
-
-
Ito, Y.1
Kusawake, T.2
Ishida, M.3
Tawa, R.4
Shibata, N.5
Takada, K.6
-
115
-
-
67549135972
-
SMEDDS of glyburide: Formulation, in vitro evaluation, and stability studies
-
Bachhav YG, Patravale VB. SMEDDS of glyburide: formulation, in vitro evaluation, and stability studies. AAPS PharmSciTech. 2009;10(2):482-487
-
(2009)
AAPS PharmSciTech.
, vol.10
, Issue.2
, pp. 482-487
-
-
Bachhav, Y.G.1
Patravale, V.B.2
-
116
-
-
0041331755
-
Examination of oral absorption and lymphatic transport of halofantrine in a triple-cannulated canine model after administration in self-microemulsifying drug delivery systems (SMEDDS) containing structured triglycerides
-
Holm R, Porter CJ, Edwards GA, Mullertz A, Kristensen HG, Charman WN. Examination of oral absorption and lymphatic transport of halofantrine in a triple-cannulated canine model after administration in self-microemulsifying drug delivery systems (SMEDDS) containing structured triglycerides. Eur J Pharm Sci. 2003;20(1):91-97
-
(2003)
Eur J Pharm Sci.
, vol.20
, Issue.1
, pp. 91-97
-
-
Holm, R.1
Porter, C.J.2
Edwards, G.A.3
Mullertz, A.4
Kristensen, H.G.5
Charman, W.N.6
-
117
-
-
62949143077
-
Studies on self-microemulsifying drug preparations of total flavones of Hippophae rhamnoides
-
Xie Y, Rong R, Li G, Yuan X, Wang J. Studies on self-microemulsifying drug preparations of total flavones of Hippophae rhamnoides. Zhongguo Zhong Yao Za Zhi. 2009;34(1):43-46
-
(2009)
Zhongguo Zhong Yao Za Zhi.
, vol.34
, Issue.1
, pp. 43-46
-
-
Xie, Y.1
Rong, R.2
Li, G.3
Yuan, X.4
Wang, J.5
-
118
-
-
33645986146
-
The novel formulation design of selfemulsifying drug delivery systems (SEDDS) type O/W microemulsion III: The permeation mechanism of a poorly water soluble drug entrapped O/W microemulsion in rat isolated intestinal membrane by the Ussing chamber method
-
Araya H, Tomita M, Hayashi M. The novel formulation design of selfemulsifying drug delivery systems (SEDDS) type O/W microemulsion III: the permeation mechanism of a poorly water soluble drug entrapped O/W microemulsion in rat isolated intestinal membrane by the Ussing chamber method. Drug Metab Pharmacokinet. 2006;21(1):45-53.
-
(2006)
Drug Metab Pharmacokinet.
, vol.21
, Issue.1
, pp. 45-53
-
-
Araya, H.1
Tomita, M.2
Hayashi, M.3
-
119
-
-
0343673791
-
Preparation and in vitro evaluation of self-microemulsifying drug delivery systems containing idebenone
-
Kim HJ, Yoon KA, Hahn M, Park ES, Chi SC. Preparation and in vitro evaluation of self-microemulsifying drug delivery systems containing idebenone. Drug Dev Ind Pharm. 2000;26(5):523-529
-
(2000)
Drug Dev Ind Pharm.
, vol.26
, Issue.5
, pp. 523-529
-
-
Kim, H.J.1
Yoon, K.A.2
Hahn, M.3
Park, E.S.4
Chi, S.C.5
-
120
-
-
0033992180
-
Enhanced absorption of indomethacin after oral or rectal administration of a self-emulsifying system containing indomethacin to rats
-
Kim JY, Ku YS. Enhanced absorption of indomethacin after oral or rectal administration of a self-emulsifying system containing indomethacin to rats. Int J Pharm. 2000;194(1):81-89
-
(2000)
Int J Pharm.
, vol.194
, Issue.1
, pp. 81-89
-
-
Kim, J.Y.1
Ku, Y.S.2
-
121
-
-
67149087355
-
Development and characterization of new indomethacin selfnanoemulsifying formulations
-
Taha EI. Development and characterization of new indomethacin selfnanoemulsifying formulations. Sci Pharm. 2009;77(2):443-451
-
(2009)
Sci Pharm.
, vol.77
, Issue.2
, pp. 443-451
-
-
Taha, E.I.1
-
122
-
-
70549086881
-
Self-microemulsifying and microemulsion systems for transdermal delivery of indomethacin: Effect of phase transition
-
El Maghraby GM. Self-microemulsifying and microemulsion systems for transdermal delivery of indomethacin: effect of phase transition. Colloids Surf B Biointerfaces. 2010;75(2):595-600.
-
(2010)
Colloids Surf B Biointerfaces.
, vol.75
, Issue.2
, pp. 595-600
-
-
El Maghraby, G.M.1
-
123
-
-
29244485443
-
A new self-emulsifying formulation of itraconazole with improved dissolution and oral absorption
-
Hong J-Y, Kim J-K, Song Y-K, Park J-S, Kim C-K. A new self-emulsifying formulation of itraconazole with improved dissolution and oral absorption. J Control Release. 2006;110(2):332-338
-
(2006)
J Control Release.
, vol.110
, Issue.2
, pp. 332-338
-
-
Hong, J.-Y.1
Kim, J.-K.2
Song, Y.-K.3
Park, J.-S.4
Kim, C.-K.5
-
124
-
-
2442698649
-
Influence of cryogenic grinding on properties of a self-emulsifying formulation
-
Chambin O, Jannin V, Champion D, Chevalier C, Rochat-Gonthier MH, Pourcelot Y. Influence of cryogenic grinding on properties of a self-emulsifying formulation. Int J Pharm. 2004;278(1):79-89.
-
(2004)
Int J Pharm.
, vol.278
, Issue.1
, pp. 79-89
-
-
Chambin, O.1
Jannin, V.2
Champion, D.3
Chevalier, C.4
Rochat-Gonthier, M.H.5
Pourcelot, Y.6
-
125
-
-
76849108463
-
Solid self-nanoemulsifying drug delivery systems (SNEDDS) of Lovastatin: Formulation development, optimization, characterization and pharmacodynamic evaluation
-
Singh B, Batra R, Bandyopadhyay S, Katare OP. Solid self-nanoemulsifying drug delivery systems (SNEDDS) of Lovastatin: formulation development, optimization, characterization and pharmacodynamic evaluation. Proceedings of the 60th Indian Pharmaceutical Congress, Delhi, India, December 12-14, 2008.
-
(2008)
Proceedings of the 60th Indian Pharmaceutical Congress, Delhi, India, December
, pp. 12-14
-
-
Singh, B.1
Batra, R.2
Bandyopadhyay, S.3
Katare, O.P.4
-
127
-
-
67349140974
-
Influence of drug polarity upon the solid-state structure and release properties of self-emulsifying drug delivery systems in relation with water affinity
-
Chambin O, Karbowiak T, Djebili L, Jannin V, Champion D, Pourcelot Y, Cayot P. Influence of drug polarity upon the solid-state structure and release properties of self-emulsifying drug delivery systems in relation with water affinity. Colloids Surf B Biointerfaces. 2009;71(1):73-78
-
(2009)
Colloids Surf B Biointerfaces.
, vol.71
, Issue.1
, pp. 73-78
-
-
Chambin, O.1
Karbowiak, T.2
Djebili, L.3
Jannin, V.4
Champion, D.5
Pourcelot, Y.6
Cayot, P.7
-
128
-
-
70350597672
-
High-throughput formulation screening system for self-microemulsifying drug delivery
-
Sakai K, Maeda H, Yoshimori T, Obata K, Ogawa Y. High-throughput formulation screening system for self-microemulsifying drug delivery. Drug Dev Ind Pharm. 2009;35(6):746-755
-
(2009)
Drug Dev Ind Pharm.
, vol.35
, Issue.6
, pp. 746-755
-
-
Sakai, K.1
Maeda, H.2
Yoshimori, T.3
Obata, K.4
Ogawa, Y.5
-
129
-
-
13544270954
-
Self-emulsifying pellets prepared by wet granulation in high-shear mixer: Influence of formulation variables and preliminary study on the in vitro absorption
-
Franceschinis E, Voinovich D, Grassi M, Perissutti B, Filipovic-Grcic J, Martinac A, Meriani-Merlo F. Self-emulsifying pellets prepared by wet granulation in high-shear mixer: influence of formulation variables and preliminary study on the in vitro absorption. Int J Pharm. 2005;291(1-2):87-97.
-
(2005)
Int J Pharm.
, vol.291
, Issue.1-2
, pp. 87-97
-
-
Franceschinis, E.1
Voinovich, D.2
Grassi, M.3
Perissutti, B.4
Filipovic-Grcic, J.5
Martinac, A.6
Meriani-Merlo, F.7
-
130
-
-
0344443710
-
Excipient effects on in vitro cytotoxicity of a novel paclitaxel self-emulsifying drug delivery system
-
Gursoy N, Garrigue JS, Razafindratsita A, Lambert G, Benita S. Excipient effects on in vitro cytotoxicity of a novel paclitaxel self-emulsifying drug delivery system. J Pharm Sci. 2003;92(12):2411-2418
-
(2003)
J Pharm Sci.
, vol.92
, Issue.12
, pp. 2411-2418
-
-
Gursoy, N.1
Garrigue, J.S.2
Razafindratsita, A.3
Lambert, G.4
Benita, S.5
-
131
-
-
20744447950
-
Enhanced oral paclitaxel absorption with vitamin E-TPGS: Effect on solubility and permeability in vitro, in situ and in vivo
-
Varma MVS, Panchagnula R. Enhanced oral paclitaxel absorption with vitamin E-TPGS: Effect on solubility and permeability in vitro, in situ and in vivo. Eur J Pharm Sci. 2005;25(4-5):445-453
-
(2005)
Eur J Pharm Sci.
, vol.25
, Issue.4-5
, pp. 445-453
-
-
Varma, M.V.S.1
Panchagnula, R.2
-
132
-
-
33748528105
-
A novel self-microemulsifying formulation of paclitaxel for oral administration to patients with advanced cancer
-
Veltkamp SA, Thijssen B, Garrigue JS, Lambert G, Lallemand F, Binlich F, Huitema AD, Nuijen B, Nol A, Beijnen JH, Schellens JH. A novel self-microemulsifying formulation of paclitaxel for oral administration to patients with advanced cancer. Br J Cancer. 2006;95(6): 729-734
-
(2006)
Br J Cancer.
, vol.95
, Issue.6
, pp. 729-734
-
-
Veltkamp, S.A.1
Thijssen, B.2
Garrigue, J.S.3
Lambert, G.4
Lallemand, F.5
Binlich, F.6
Huitema, A.D.7
Nuijen, B.8
Nol, A.9
Beijnen, J.H.10
Schellens, J.H.11
-
133
-
-
6944249393
-
Controlled release of paclitaxel from microemulsion containing PLGA and evaluation of anti-tumor activity in vitro and in vivo
-
Kang BK, Chon SK, Kim SH, Jeong SY, Kim MS, Cho SH, Lee HB, Khang G. Controlled release of paclitaxel from microemulsion containing PLGA and evaluation of anti-tumor activity in vitro and in vivo. Int J Pharm. 2004;286(1-2):147-156
-
(2004)
Int J Pharm.
, vol.286
, Issue.1-2
, pp. 147-156
-
-
Kang, B.K.1
Chon, S.K.2
Kim, S.H.3
Jeong, S.Y.4
Kim, M.S.5
Cho, S.H.6
Lee, H.B.7
Khang, G.8
-
134
-
-
77951278963
-
Self-emulsifying O/W formulations of paclitaxel prepared from mixed nonionic surfactants
-
Lo JT, Chen BH, Lee TM, Han J, Li JL. Self-emulsifying O/W formulations of paclitaxel prepared from mixed nonionic surfactants. J Pharm Sci. 2009 Nov 5. [Epub ahead of print]
-
(2009)
J Pharm Sci.
, vol.5
-
-
Lo, J.T.1
Chen, B.H.2
Lee, T.M.3
Han, J.4
Li, J.L.5
-
135
-
-
31544477756
-
Pharmacodynamics of piroxicam from self-emulsifying lipospheres formulated with homolipids extracted from Capra hircus
-
Attama AA, Mpamaugo VE. Pharmacodynamics of piroxicam from self-emulsifying lipospheres formulated with homolipids extracted from Capra hircus. Drug Deliv. 2006;13(2):133-137
-
(2006)
Drug Deliv.
, vol.13
, Issue.2
, pp. 133-137
-
-
Attama, A.A.1
Mpamaugo, V.E.2
-
136
-
-
44649084933
-
Design and in vitro evaluation of self-microemulsifying drug delivery systems for piroxicam
-
Zhou XT, Wang J, Wang Y, Sun JY, Nie SF, Pan WS. Design and in vitro evaluation of self-microemulsifying drug delivery systems for piroxicam. Yao Xue Xue Bao. 2008;43(4):415-420
-
(2008)
Yao Xue Xue Bao.
, vol.43
, Issue.4
, pp. 415-420
-
-
Zhou, X.T.1
Wang, J.2
Wang, Y.3
Sun, J.Y.4
Nie, S.F.5
Pan, W.S.6
-
137
-
-
21344438401
-
Enzymatic characterization of lipid-based drug delivery systems
-
Ljusberg-Wahren H, Seier Nielsen F, Brogård M, Troedsson E, Müllertz A. Enzymatic characterization of lipid-based drug delivery systems. Int J Pharm. 2005;298(2):328-332
-
(2005)
Int J Pharm.
, vol.298
, Issue.2
, pp. 328-332
-
-
Ljusberg-Wahren, H.1
Seier Nielsen, F.2
Brogård, M.3
Troedsson, E.4
Müllertz, A.5
-
138
-
-
0030298897
-
Positively charged self-emulsifying oil formulation for improving oral bioavailability of progesterone
-
Gershanik T, Benita S. Positively charged self-emulsifying oil formulation for improving oral bioavailability of progesterone. Pharm Dev Technol. 1996;1(2):147-157
-
(1996)
Pharm Dev Technol.
, vol.1
, Issue.2
, pp. 147-157
-
-
Gershanik, T.1
Benita, S.2
-
139
-
-
2642540226
-
Comparative bioavailability study in dogs of a self-emulsifying formulation of progesterone presented in a pellet and liquid form compared with an aqueous suspension of progesterone
-
Tuleu C, Newton M, Rose J, Euler D, Saklatvala R, Clarke A, Booth S. Comparative bioavailability study in dogs of a self-emulsifying formulation of progesterone presented in a pellet and liquid form compared with an aqueous suspension of progesterone. J Pharm Sci. 2004;93(6):1495-1502
-
(2004)
J Pharm Sci.
, vol.93
, Issue.6
, pp. 1495-1502
-
-
Tuleu, C.1
Newton, M.2
Rose, J.3
Euler, D.4
Saklatvala, R.5
Clarke, A.6
Booth, S.7
-
140
-
-
42149188225
-
Formulation optimization of self-emulsifying preparations of puerarin through self-emulsifying performances evaluation in vitro and pharmacokinetic studies in vivo
-
Quan DQ, Xu GX. Formulation optimization of self-emulsifying preparations of puerarin through self-emulsifying performances evaluation in vitro and pharmacokinetic studies in vivo. Yao Xue Xue Bao. 2007;42(8):886-891
-
(2007)
Yao Xue Xue Bao.
, vol.42
, Issue.8
, pp. 886-891
-
-
Quan, D.Q.1
Xu, G.X.2
-
141
-
-
39049194064
-
Preparation of puerarin solid selfmicroemulsion
-
Yu AH, Zhai GX, Cui J, Liu H. Preparation of puerarin solid selfmicroemulsion. Zhong Yao Cai. 2006;29(8):834-838
-
(2006)
Zhong Yao Cai.
, vol.29
, Issue.8
, pp. 834-838
-
-
Yu, A.H.1
Zhai, G.X.2
Cui, J.3
Liu, H.4
-
142
-
-
76849117001
-
Self nano-emulsifying drug delivery systems (SNEDDS) of raloxifene hydrochloride: Formulation, evaluation and optimization [abstract 42]
-
Ahuja N, Kataria A, Bandyopadhyay S, Singh B. Self nano-emulsifying drug delivery systems (SNEDDS) of raloxifene hydrochloride: formulation, evaluation and optimization [abstract 42]. Proceedings of the 3rd Chandigarh Science Congress (CHASCON), Panjab University, Chandigarh, India, February 26-28, 2009.
-
(2009)
Proceedings of the 3rd Chandigarh Science Congress (CHASCON), Panjab University, Chandigarh, India, February
, pp. 26-28
-
-
Ahuja, N.1
Kataria, A.2
Bandyopadhyay, S.3
Singh, B.4
-
143
-
-
33646813333
-
Bioavailability of seocalcitol II: Development and characterisation of self-microemulsifying drug delivery systems (SMEDDS) for oral administration containing medium and long chain triglycerides
-
Grove M, Mullertz A, Nielsen JL, Pedersen GP. Bioavailability of seocalcitol II: development and characterisation of self-microemulsifying drug delivery systems (SMEDDS) for oral administration containing medium and long chain triglycerides. Eur J Pharm Sci. 2006;28(3):233-242
-
(2006)
Eur J Pharm Sci.
, vol.28
, Issue.3
, pp. 233-242
-
-
Grove, M.1
Mullertz, A.2
Nielsen, J.L.3
Pedersen, G.P.4
-
144
-
-
34247137899
-
Bioavailability of seocalcitol III: Administration of lipid-based formulations to minipigs in the fasted and fed state
-
Grove M, Mullertz A, Pedersen GP, Nielsen JL. Bioavailability of seocalcitol III: administration of lipid-based formulations to minipigs in the fasted and fed state. Eur J Pharm Sci. 2007;31(1):8-15.
-
(2007)
Eur J Pharm Sci.
, vol.31
, Issue.1
, pp. 8-15
-
-
Grove, M.1
Mullertz, A.2
Pedersen, G.P.3
Nielsen, J.L.4
-
145
-
-
1842609789
-
Development of self-microemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogs
-
Kang BK, Lee JS, Chon SK, Jeong SY, Yuk SH, Khang G, Lee HB, Cho SH. Development of self-microemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogs. Int J Pharm. 2004;274(1-2):65-73.
-
(2004)
Int J Pharm.
, vol.274
, Issue.1-2
, pp. 65-73
-
-
Kang, B.K.1
Lee, J.S.2
Chon, S.K.3
Jeong, S.Y.4
Yuk, S.H.5
Khang, G.6
Lee, H.B.7
Cho, S.H.8
-
146
-
-
69749105594
-
Self-nanoemulsifying drug delivery systems of tamoxifen citrate: Design and optimization
-
Elnaggar YS, El-Massik MA, Abdallah OY. Self-nanoemulsifying drug delivery systems of tamoxifen citrate: design and optimization. Int J Pharm. 2009;380(1-2):133-141
-
(2009)
Int J Pharm.
, vol.380
, Issue.1-2
, pp. 133-141
-
-
Elnaggar, Y.S.1
El-Massik, M.A.2
Abdallah, O.Y.3
-
147
-
-
0037142237
-
Optimization of a self-nanoemulsified tablet dosage form of Ubiquinone using response surface methodology: Effect of formulation ingredients
-
Nazzal S, Nutan M, Palamakula A, Shah R, Zaghloul AA, Khan MA. Optimization of a self-nanoemulsified tablet dosage form of Ubiquinone using response surface methodology: effect of formulation ingredients. Int J Pharm. 2002;240(1-2):103-114
-
(2002)
Int J Pharm.
, vol.240
, Issue.1-2
, pp. 103-114
-
-
Nazzal, S.1
Nutan, M.2
Palamakula, A.3
Shah, R.4
Zaghloul, A.A.5
Khan, M.A.6
-
148
-
-
34247489694
-
Correlation between digestion of the lipid phase of smedds and release of the anti-HIV drug UC 781 and the anti-mycotic drug enilconazole from smedds
-
Goddeeris C, Coacci J, Van den Mooter G. Correlation between digestion of the lipid phase of smedds and release of the anti-HIV drug UC 781 and the anti-mycotic drug enilconazole from smedds. Eur J Pharm Biopharm. 2007;66(2):173-181
-
(2007)
Eur J Pharm Biopharm.
, vol.66
, Issue.2
, pp. 173-181
-
-
Goddeeris, C.1
Coacci, J.2
Van Den Mooter, G.3
-
149
-
-
37849030987
-
Selfmicroemulsifying drug delivery system (SMEDDS) of vinpocetine: Formulation development and in vivo assessment
-
Chen Y, Li G, Wu X, Chen Z, Hang J, Qin B, Chen S, Wang R. Selfmicroemulsifying drug delivery system (SMEDDS) of vinpocetine: formulation development and in vivo assessment. Biol Pharm Bull. 2008;31(1):118-125
-
(2008)
Biol Pharm Bull.
, vol.31
, Issue.1
, pp. 118-125
-
-
Chen, Y.1
Li, G.2
Wu, X.3
Chen, Z.4
Hang, J.5
Qin, B.6
Chen, S.7
Wang, R.8
-
150
-
-
0343963156
-
Improved bioavailability of vitamin e with a self emulsifying formulation
-
Julianto T, Yuen KH, Noor AM. Improved bioavailability of vitamin E with a self emulsifying formulation. Int J Pharm. 2000;200(1):53-57
-
(2000)
Int J Pharm.
, vol.200
, Issue.1
, pp. 53-57
-
-
Julianto, T.1
Yuen, K.H.2
Noor, A.M.3
-
151
-
-
39549095134
-
Comparison between lipolysis and compendial dissolution as alternative techniques for the in vitro characterization of alpha-tocopherol self-emulsified drug delivery systems (SEDDS
-
Ali H, Nazzal M, Zaghloul AA, Nazzal S. Comparison between lipolysis and compendial dissolution as alternative techniques for the in vitro characterization of alpha-tocopherol self-emulsified drug delivery systems (SEDDS). Int J Pharm. 2008;352(1-2):104-114
-
(2008)
Int J Pharm.
, vol.352
, Issue.1-2
, pp. 104-114
-
-
Ali, H.1
Nazzal, M.2
Zaghloul, A.A.3
Nazzal, S.4
-
152
-
-
34447333390
-
Liquid spray formulations of xibornol by using self-microemulsifying drug delivery systems
-
Cirri M, Mura P, Mora PC. Liquid spray formulations of xibornol by using self-microemulsifying drug delivery systems. Int J Pharm. 2007;340(1-2):84-91.
-
(2007)
Int J Pharm.
, vol.340
, Issue.1-2
, pp. 84-91
-
-
Cirri, M.1
Mura, P.2
Mora, P.C.3
-
153
-
-
59849110173
-
Characterization and optimization of AMG 517 supersaturatable self-emulsifying drug delivery system (S-SEDDS) for improved oral absorption
-
Gao P, Akrami A, Alvarez F, Hu J, Li L, Ma C, Surapaneni S. Characterization and optimization of AMG 517 supersaturatable self-emulsifying drug delivery system (S-SEDDS) for improved oral absorption. J Pharm Sci. 2009;98(2):516-528
-
(2009)
J Pharm Sci.
, vol.98
, Issue.2
, pp. 516-528
-
-
Gao, P.1
Akrami, A.2
Alvarez, F.3
Hu, J.4
Li, L.5
Ma, C.6
Surapaneni, S.7
-
154
-
-
0024266630
-
Supersaturation mechanism of drugs from solid dispersions with enteric coating agents
-
Hasegawa A, Taguchi M, Suzuki R, Miyata T, Nakagawa H, Sugimoto I. Supersaturation mechanism of drugs from solid dispersions with enteric coating agents. Chem Pharm Bull (Tokyo). 1988;36(12):4941-4950
-
(1988)
Chem Pharm Bull (Tokyo
, vol.36
, Issue.12
, pp. 4941-4950
-
-
Hasegawa, A.1
Taguchi, M.2
Suzuki, R.3
Miyata, T.4
Nakagawa, H.5
Sugimoto, I.6
-
155
-
-
0030899727
-
The penetration of supersaturated solutions of piroxicam across silicone membranes and human skin in vitro
-
Pellett MA, Castellano S, Hadgraft J, Davis AF. The penetration of supersaturated solutions of piroxicam across silicone membranes and human skin in vitro. J Control Release. 1997;46(3):205-214
-
(1997)
J Control Release.
, vol.46
, Issue.3
, pp. 205-214
-
-
Pellett, M.A.1
Castellano, S.2
Hadgraft, J.3
Davis, A.F.4
-
156
-
-
0035912915
-
Membrane transport of hydrocortisone acetate from supersaturated solutions; The role of polymers
-
Raghavan SL, Kiepfer B, Davis AF, Kazarian SG, Hadgraft J. Membrane transport of hydrocortisone acetate from supersaturated solutions; the role of polymers. Int J Pharm. 2001;221(1-2):95-105.
-
(2001)
Int J Pharm.
, vol.221
, Issue.1-2
, pp. 95-105
-
-
Raghavan, S.L.1
Kiepfer, B.2
Davis, A.F.3
Kazarian, S.G.4
Hadgraft, J.5
-
157
-
-
45849150105
-
Conventional and alternative pharmaceutical methods to improve oral bioavailability of lipophilic drugs
-
Prajapati BG, Patel MM. Conventional and alternative pharmaceutical methods to improve oral bioavailability of lipophilic drugs. Asian J Pharm. 2007;1:1-8.
-
(2007)
Asian J Pharm.
, vol.1
, pp. 1-8
-
-
Prajapati, B.G.1
Patel, M.M.2
-
158
-
-
55949089032
-
A new self-emulsifying drug delivery system (SEDDS) for poorly soluble drugs: Characterization, dissolution, in vitro digestion and incorporation into solid pellets
-
Abdalla A, Klein S, Mader K. A new self-emulsifying drug delivery system (SEDDS) for poorly soluble drugs: characterization, dissolution, in vitro digestion and incorporation into solid pellets. Eur J Pharm Sci. 2008;35(5):457-464
-
(2008)
Eur J Pharm Sci.
, vol.35
, Issue.5
, pp. 457-464
-
-
Abdalla, A.1
Klein, S.2
Mader, K.3
-
159
-
-
52949125231
-
A new solid self-microemulsifying formulation prepared by spray-drying to improve the oral bioavailability of poorly water soluble drugs
-
Yi T, Wan J, Xu H, Yang X. A new solid self-microemulsifying formulation prepared by spray-drying to improve the oral bioavailability of poorly water soluble drugs. Eur J Pharm Biopharm. 2008;70(2):439-444
-
(2008)
Eur J Pharm Biopharm.
, vol.70
, Issue.2
, pp. 439-444
-
-
Yi, T.1
Wan, J.2
Xu, H.3
Yang, X.4
-
160
-
-
0035667509
-
Enhanced drug dissolution and bulk properties of solid dispersions granulated with a surface adsorbent
-
Gupta MK, Goldman D, Bogner RH, Tseng YC. Enhanced drug dissolution and bulk properties of solid dispersions granulated with a surface adsorbent. Pharm Dev Technol. 2001;6(4):563-572
-
(2001)
Pharm Dev Technol.
, vol.6
, Issue.4
, pp. 563-572
-
-
Gupta, M.K.1
Goldman, D.2
Bogner, R.H.3
Tseng, Y.C.4
-
161
-
-
0036844753
-
Hydrogen bonding with adsorbent during storage governs drug dissolution from solid-dispersion granules
-
DOI 10.1023/A:1020905412654
-
Gupta MK, Tseng YC, Goldman D, Bogner RH. Hydrogen bonding with adsorbent during storage governs drug dissolution from solid-dispersion granules. Pharm Res. 2002;19(11):1663-1672 (Pubitemid 35305518)
-
(2002)
Pharmaceutical Research
, vol.19
, Issue.11
, pp. 1663-1672
-
-
Gupta, M.K.1
Tseng, Y.-C.2
Goldman, D.3
Bogner, R.H.4
-
162
-
-
33847148114
-
The preparation of pellets containing a surfactant or a mixture of mono- and di-glycerides by extrusion/ spheronization
-
Newton JM, Pinto MR, Podczeck F. The preparation of pellets containing a surfactant or a mixture of mono- and di-glycerides by extrusion/ spheronization. Eur J Pharm Sci. 2007;30(3-4):333-342
-
(2007)
Eur J Pharm Sci.
, vol.30
, Issue.3-4
, pp. 333-342
-
-
Newton, J.M.1
Pinto, M.R.2
Podczeck, F.3
-
163
-
-
43249131737
-
Bi-layered self-emulsifying pellets prepared by co-extrusion and spheronization: Influence of formulation variables and preliminary study on the in vivo absorption
-
Iosio T, Voinovich D, Grassi M, Pinto JF, Perissutti B, Zacchigna M, Quintavalle U, Serdoz F. Bi-layered self-emulsifying pellets prepared by co-extrusion and spheronization: influence of formulation variables and preliminary study on the in vivo absorption. Eur J Pharm Biopharm. 2008;69(2):686-697
-
(2008)
Eur J Pharm Biopharm.
, vol.69
, Issue.2
, pp. 686-697
-
-
Iosio, T.1
Voinovich, D.2
Grassi, M.3
Pinto, J.F.4
Perissutti, B.5
Zacchigna, M.6
Quintavalle, U.7
Serdoz, F.8
-
164
-
-
38949117575
-
Approaches for the development of solid and semi-solid lipid-based formulations
-
Jannin V, Musakhanian J, Marchaud D. Approaches for the development of solid and semi-solid lipid-based formulations. Adv Drug Deliv Rev. 2008;60(6):734-746
-
(2008)
Adv Drug Deliv Rev.
, vol.60
, Issue.6
, pp. 734-746
-
-
Jannin, V.1
Musakhanian, J.2
Marchaud, D.3
-
165
-
-
33646383855
-
Controlled release of a self-emulsifying formulation from a tablet dosage form: Stability assessment and optimization of some processing parameters
-
Nazzal S, Khan MA. Controlled release of a self-emulsifying formulation
-
(2006)
Int J Pharm.
, vol.315
, Issue.1-2
, pp. 110-121
-
-
Nazzal, S.1
Khan, M.A.2
-
166
-
-
13544270954
-
Self-emulsifying pellets prepared by wet granulation in high-shear mixer: Influence of formulation variables and preliminary study on the in vitro absorption
-
Franceschinis E, Voinovich D, Grassi M, Perissutti B, Filipovic-Grcic J, Martinac A, Meriani-Merlo F. Self-emulsifying pellets prepared by wet granulation in high-shear mixer: influence of formulation variables and preliminary study on the in vitro absorption. Int J Pharm. 2005;291(1-2):87-97.
-
(2005)
Int J Pharm.
, vol.291
, Issue.1-2
, pp. 87-97
-
-
Franceschinis, E.1
Voinovich, D.2
Grassi, M.3
Perissutti, B.4
Filipovic-Grcic, J.5
Martinac, A.6
Meriani-Merlo, F.7
-
167
-
-
50449091497
-
Self-nanoemulsifying granules of ezetimibe: Design, optimization and evaluation
-
Dixit RP, Nagarsenker MS. Self-nanoemulsifying granules of ezetimibe: design, optimization and evaluation. Eur J Pharm Sci. 2008;35(3):183-192
-
(2008)
Eur J Pharm Sci.
, vol.35
, Issue.3
, pp. 183-192
-
-
Dixit, R.P.1
Nagarsenker, M.S.2
-
168
-
-
0031399482
-
Enhancement and modification of etoposide release from crospovidone particles loaded with oil-surfactant blends
-
Boltri L, Coceani N, De Curto D, Dobetti L, Esposito P. Enhancement and modification of etoposide release from crospovidone particles loaded with oil-surfactant blends. Pharm Dev Technol. 1997;2(4):373-381
-
(1997)
Pharm Dev Technol.
, vol.2
, Issue.4
, pp. 373-381
-
-
Boltri, L.1
Coceani, N.2
De Curto, D.3
Dobetti, L.4
Esposito, P.5
-
169
-
-
47249128905
-
Controlled poorly soluble drug release from solid self-microemulsifying formulations with high viscosity hydroxypropylmethylcellulose
-
Yi T, Wan J, Xu H, Yang X. Controlled poorly soluble drug release from solid self-microemulsifying formulations with high viscosity hydroxypropylmethylcellulose. Eur J Pharm Sci. 2008;34(4-5):274-280
-
(2008)
Eur J Pharm Sci.
, vol.34
, Issue.4-5
, pp. 274-280
-
-
Yi, T.1
Wan, J.2
Xu, H.3
Yang, X.4
-
170
-
-
84896445903
-
Improving Bioavailability of simvastatin using various types of Self emulsifying formulations
-
Dehal S, Bandyopadhyay S, Singh B. Improving Bioavailability of simvastatin using various types of Self emulsifying formulations. Proceedings of the 30th Annual Conference of Indian Association of Biomedical Scientists, Defence Institute of High Altitude Research, Chandigarh, India, November 18-20, 2009.
-
(2009)
Proceedings of the 30th Annual Conference of Indian Association of Biomedical Scientists, Defence Institute of High Altitude Research, Chandigarh, India, November
, pp. 18-20
-
-
Dehal, S.1
Bandyopadhyay, S.2
Singh, B.3
-
171
-
-
0034889914
-
The influence of formulation variables on the properties of pellets containing a selfemulsifying mixture
-
Newton M, Petersson J, Podczeck F, Clarke A, Booth S. The influence of formulation variables on the properties of pellets containing a selfemulsifying mixture. J Pharm Sci. 2001;90(8):987-995
-
(2001)
J Pharm Sci.
, vol.90
, Issue.8
, pp. 987-995
-
-
Newton, M.1
Petersson, J.2
Podczeck, F.3
Clarke, A.4
Booth, S.5
-
172
-
-
40549142737
-
Solid self-nanoemulsifying delivery systems as a platform technology for formulation of poorly soluble drugs
-
Bansal T, Mustafa G, Khan ZI, Ahmad FJ, Khar RK, Talegaonkar S. Solid self-nanoemulsifying delivery systems as a platform technology for formulation of poorly soluble drugs. Crit Rev Ther Drug Carrier Syst. 2008;25(1):63-116.
-
(2008)
Crit Rev Ther Drug Carrier Syst.
, vol.25
, Issue.1
, pp. 63-116
-
-
Bansal, T.1
Mustafa, G.2
Khan, Z.I.3
Ahmad, F.J.4
Khar, R.K.5
Talegaonkar, S.6
-
174
-
-
27944493214
-
Integrated approaches towards drug development from Ayurveda and other Indian system of medicines
-
Mukherjee PK, Wahile A. Integrated approaches towards drug development from Ayurveda and other Indian system of medicines. J Ethnopharmacol. 2006;103(1):25-35.
-
(2006)
J Ethnopharmacol.
, vol.103
, Issue.1
, pp. 25-35
-
-
Mukherjee, P.K.1
Wahile, A.2
-
177
-
-
0015444348
-
Membrane potentials of epithelial cells in rat small intestine
-
Barry RJ, Eggenton J. Membrane potentials of epithelial cells in rat small intestine. J Physiol. 1972;227(1):201-216
-
(1972)
J Physiol.
, vol.227
, Issue.1
, pp. 201-216
-
-
Barry, R.J.1
Eggenton, J.2
-
178
-
-
0025253424
-
Characterization of the barrier properties of mucosal membranes
-
Corbo DC, Liu JC, Chien YW. Characterization of the barrier properties of mucosal membranes. J Pharm Sci. 1990;79(3):202-206
-
(1990)
J Pharm Sci.
, vol.79
, Issue.3
, pp. 202-206
-
-
Corbo, D.C.1
Liu, J.C.2
Chien, Y.W.3
-
179
-
-
0026666843
-
The transport barrier of epithelia: A comparative study on membrane permeability and charge selectivity in the rabbit
-
Rojanasakul Y, Wang LY, Bhat M, Glover DD, Malanga CJ, Ma JK. The transport barrier of epithelia: a comparative study on membrane permeability and charge selectivity in the rabbit. Pharm Res. 1992;9(8):1029-1034
-
(1992)
Pharm Res.
, vol.9
, Issue.8
, pp. 1029-1034
-
-
Rojanasakul, Y.1
Wang, L.Y.2
Bhat, M.3
Glover, D.D.4
Malanga, C.J.5
Ma, J.K.6
-
181
-
-
21644477111
-
Classification of loratadine based on the biopharmaceutics drug classification concept and possible in vitro-in vivo correlation
-
Khan MZI, Rasul D, Zanoski Rea. Classification of loratadine based on the biopharmaceutics drug classification concept and possible in vitro-in vivo correlation. Biol Pharm Bull. 2004;27:1630-1635
-
(2004)
Biol Pharm Bull.
, vol.27
, pp. 1630-1635
-
-
Khan, M.Z.I.1
Rasul, D.2
Zanoski, Rea.3
-
182
-
-
33751518550
-
Controlled drug release from pellets containing water-insoluble drugs dissolved in a self-emulsifying system
-
Serratoni M, Newton M, Booth S, Clarke A. Controlled drug release from pellets containing water-insoluble drugs dissolved in a self-emulsifying system. Eur J Pharm Biopharm. 2007;65(1):94-98
-
(2007)
Eur J Pharm Biopharm.
, vol.65
, Issue.1
, pp. 94-98
-
-
Serratoni, M.1
Newton, M.2
Booth, S.3
Clarke, A.4
-
183
-
-
70449532105
-
Solid self-emulsifying nitrendipine pellets: Preparation and in vitro/in vivo evaluation
-
Wang Z, Sun J, Wang Y, Liu X, Liu Y, Fu Q, Meng P, He Z. Solid self-emulsifying nitrendipine pellets: preparation and in vitro/in vivo evaluation. Int J Pharm. 2010;383(1-2):1-6.
-
(2010)
Int J Pharm.
, vol.383
, Issue.1-2
, pp. 1-6
-
-
Wang, Z.1
Sun, J.2
Wang, Y.3
Liu, X.4
Liu, Y.5
Fu, Q.6
Meng, P.7
He, Z.8
-
184
-
-
69449090008
-
Preparation, in vitro and in vivo evaluation of solid-state self-nanoemulsifying drug delivery system (SNEDDS) of vitamin A acetate
-
Taha EI, Al-Suwayeh SA, Anwer MK. Preparation, in vitro and in vivo evaluation of solid-state self-nanoemulsifying drug delivery system (SNEDDS) of vitamin A acetate. J Drug Target. 2009;17(6):468-473
-
(2009)
J Drug Target.
, vol.17
, Issue.6
, pp. 468-473
-
-
Taha, E.I.1
Al-Suwayeh, S.A.2
Anwer, M.K.3
-
186
-
-
62749095208
-
Enhancement of oral absorption of curcumin by self-microemulsifying drug delivery systems
-
Cui J, Yu B, Zhao Y, Zhu W, Li H, Lou H, Zhai G. Enhancement of oral absorption of curcumin by self-microemulsifying drug delivery systems. Int J Pharm. 2009;371(1-2):148-155
-
(2009)
Int J Pharm.
, vol.371
, Issue.1-2
, pp. 148-155
-
-
Cui, J.1
Yu, B.2
Zhao, Y.3
Zhu, W.4
Li, H.5
Lou, H.6
Zhai, G.7
-
187
-
-
70449786950
-
Study on self-microemulsifying drug delivery system of Jiaotai Pill active components
-
Zhang BE, Lu WB, Chen WW. Study on self-microemulsifying drug delivery system of Jiaotai Pill active components. Zhong Yao Cai. 2008;31(7):1068-1071
-
(2008)
Zhong Yao Cai.
, vol.31
, Issue.7
, pp. 1068-1071
-
-
Zhang, B.E.1
Lu, W.B.2
Chen, W.W.3
-
188
-
-
36948999846
-
-
Cai Q, Liang L, Huang YP, Hou SX. In vitro evaluation of self-emulsifying drug delivery system of volatile oil from rhizome of Ligusticum chuanxiong. Zhongguo Zhong Yao Za Zhi. 2007;32(19):2003-2007
-
(2007)
In Vitro Evaluation of Self-emulsifying Drug Delivery System of Volatile Oil from Rhizome of Ligusticum Chuanxiong. Zhongguo Zhong Yao Za Zhi
, vol.32
, Issue.19
, pp. 2003-2007
-
-
Cai, Q.1
Liang, L.2
Huang, Y.P.3
Hou, S.X.4
-
189
-
-
41449094532
-
Preparation of self-microemusifying drug delivery system for volatile oil from rhizome of ligusticum Chuanxiong
-
Mar
-
Cai Q, Liang L, Hou SX, Huang YP. Preparation of self-microemusifying drug delivery system for volatile oil from rhizome of ligusticum Chuanxiong. Sichuan Da Xue Xue Bao Yi Xue Ban. 2008 Mar;39(2):312-314
-
(2008)
Sichuan da Xue Xue Bao Yi Xue Ban
, vol.39
, Issue.2
, pp. 312-314
-
-
Cai, Q.1
Liang, L.2
Hou, S.X.3
Huang, Y.P.4
-
190
-
-
58149125516
-
Preparation of nobiletin in self-microemulsifying systems and its intestinal permeability in rats
-
Yao J, Lu Y, Zhou JP. Preparation of nobiletin in self-microemulsifying systems and its intestinal permeability in rats. J Pharm Pharm Sci. 2008;11(3):22-29
-
(2008)
J Pharm Pharm Sci.
, vol.11
, Issue.3
, pp. 22-29
-
-
Yao, J.1
Lu, Y.2
Zhou, J.P.3
-
191
-
-
41349096647
-
Preparation and evaluation of selfmicroemulsifying drug delivery system of oridonin
-
Zhang P, Liu Y, Feng N, Xu J. Preparation and evaluation of selfmicroemulsifying drug delivery system of oridonin. Int J Pharm. 2008;355(1-2):269-276
-
(2008)
Int J Pharm.
, vol.355
, Issue.1-2
, pp. 269-276
-
-
Zhang, P.1
Liu, Y.2
Feng, N.3
Xu, J.4
-
192
-
-
24744442330
-
Self-microemulsifying drug delivery systems (SMEDDS) for improving in vitro dissolution and oral absorption of Pueraria lobata isoflavone
-
Cui S, Zhao C, Chen D, He Z. Self-microemulsifying drug delivery systems (SMEDDS) for improving in vitro dissolution and oral absorption of Pueraria lobata isoflavone. Drug Dev Ind Pharm. 2005;31(4-5): 349-356
-
(2005)
Drug Dev Ind Pharm.
, vol.31
, Issue.4-5
, pp. 349-356
-
-
Cui, S.1
Zhao, C.2
Chen, D.3
He, Z.4
-
193
-
-
33847642532
-
Formulation development and pharmacokinetics of puerarin self-emulsifying drug delivery systems
-
Dong-Qin Q, Gui-Xia X, Xiang-Gen W. Formulation development and pharmacokinetics of puerarin self-emulsifying drug delivery systems. PDA J Pharm Sci Technol. 2007;61(1):37-43.
-
(2007)
PDA J Pharm Sci Technol.
, vol.61
, Issue.1
, pp. 37-43
-
-
Dong-Qin, Q.1
Gui-Xia, X.2
Xiang-Gen, W.3
-
194
-
-
34248169123
-
Studies on preparation and absolute bioavailability of a self-emulsifying system containing puerarin
-
Quan DQ, Xu GX, Wu XG. Studies on preparation and absolute bioavailability of a self-emulsifying system containing puerarin. Chem Pharm Bull (Tokyo). 2007;55(5):800-803
-
(2007)
Chem Pharm Bull (Tokyo
, vol.55
, Issue.5
, pp. 800-803
-
-
Quan, D.Q.1
Xu, G.X.2
Wu, X.G.3
-
195
-
-
33646854907
-
Enhanced bioavailability of silymarin by self-microemulsifying drug delivery system
-
Wu W, Wang Y, Que L. Enhanced bioavailability of silymarin by self-microemulsifying drug delivery system. Eur J Pharm Biopharm. 2006;63(3):288-294
-
(2006)
Eur J Pharm Biopharm.
, vol.63
, Issue.3
, pp. 288-294
-
-
Wu, W.1
Wang, Y.2
Que, L.3
-
196
-
-
33846839082
-
Formulation and biopharmaceutical evaluation of silymarin using SMEDDS
-
Woo JS, Kim TS, Park JH, Chi SC. Formulation and biopharmaceutical evaluation of silymarin using SMEDDS. Arch Pharm Res. 2007;30(1):82-89
-
(2007)
Arch Pharm Res.
, vol.30
, Issue.1
, pp. 82-89
-
-
Woo, J.S.1
Kim, T.S.2
Park, J.H.3
Chi, S.C.4
-
197
-
-
11144249850
-
A novel formulation design about water-insoluble oily drug: Preparation of zedoary turmeric oil microspheres with self-emulsifying ability and evaluation in rabbits
-
You J, Cui F-D, Li Q-P, Han X, Yu Y-W, Yang M-S. A novel formulation design about water-insoluble oily drug: preparation of zedoary turmeric oil microspheres with self-emulsifying ability and evaluation in rabbits. Int J Pharm. 2005;288(2):315-323
-
(2005)
Int J Pharm.
, vol.288
, Issue.2
, pp. 315-323
-
-
You, J.1
Cui, F.-D.2
Li, Q.-P.3
Han, X.4
Yu, Y.-W.5
Yang, M.-S.6
-
198
-
-
50549097100
-
Development of SMEDDS using natural lipophile: Application to beta-artemether delivery
-
Mandawgade SD, Sharma S, Pathak S, Patravale VB. Development of SMEDDS using natural lipophile: application to beta-artemether delivery. Int J Pharm. 2008;362(1-2):179-183
-
(2008)
Int J Pharm.
, vol.362
, Issue.1-2
, pp. 179-183
-
-
Mandawgade, S.D.1
Sharma, S.2
Pathak, S.3
Patravale, V.B.4
-
199
-
-
72449150202
-
Development and characterization of a carvedilol-loaded self-microemulsifying delivery system
-
Singh SK, Verma PRP, Razdan B. Development and characterization of a carvedilol-loaded self-microemulsifying delivery system. Clin Res Regulat Affairs. 2009;26(3):50-64.
-
(2009)
Clin Res Regulat Affairs.
, vol.26
, Issue.3
, pp. 50-64
-
-
Singh, S.K.1
Verma, P.R.P.2
Razdan, B.3
-
200
-
-
76849116015
-
Development and characterization of a lovastatin-loaded self-microemulsifying drug delivery system
-
Oct 1. [Epub ahead of print]
-
Singh SK, Verma PR, Razdan B. Development and characterization of a lovastatin-loaded self-microemulsifying drug delivery system. Pharm Dev Technol. 2009 Oct 1. [Epub ahead of print]
-
(2009)
Pharm Dev Technol.
-
-
Singh, S.K.1
Verma, P.R.2
Razdan, B.3
-
201
-
-
0034671698
-
Charge-dependent interaction of self-emulsifying oil formulations with Caco-2 cells monolayers: Binding, effects on barrier function and cytotoxicity
-
Gershanik T, Haltner E, Lehr CM, Benita S. Charge-dependent interaction of self-emulsifying oil formulations with Caco-2 cells monolayers: binding, effects on barrier function and cytotoxicity. Int J Pharm. 2000;211(1-2):29-36.
-
(2000)
Int J Pharm.
, vol.211
, Issue.1-2
, pp. 29-36
-
-
Gershanik, T.1
Haltner, E.2
Lehr, C.M.3
Benita, S.4
-
202
-
-
0016213586
-
Fusion of mouse fibroblasts with oleylamine
-
Bruckdorfer KR, Cramp FC, Goodall AH, Verrinder M, Lucy JA. Fusion of mouse fibroblasts with oleylamine. J Cell Sci. 1974;15(1): 185-199
-
(1974)
J Cell Sci.
, vol.15
, Issue.1
, pp. 185-199
-
-
Bruckdorfer, K.R.1
Cramp, F.C.2
Goodall, A.H.3
Verrinder, M.4
Lucy, J.A.5
-
203
-
-
70349562924
-
Preparation and performance evaluation of saquinavir laden cationic submicron emulsions
-
Jain V, Prasad V, Jadhav P, Mishra PR. Preparation and performance evaluation of saquinavir laden cationic submicron emulsions. Drug Deliv. 2009;16(1):37-44.
-
(2009)
Drug Deliv.
, vol.16
, Issue.1
, pp. 37-44
-
-
Jain, V.1
Prasad, V.2
Jadhav, P.3
Mishra, P.R.4
-
204
-
-
76849087325
-
-
J. Swarbrick, J.C. Boylan, Editors.
-
Lewis GA, Optmization methods, in Encyclopedia of pharmaceutical technology, J. Swarbrick, J.C. Boylan, Editors. 2002, Marcel Dekker, Inc.: New York. p. 1922-1937
-
(2002)
Optmization Methods, in Encyclopedia of Pharmaceutical Technology
, pp. 1922-1937
-
-
Lewis, G.A.1
-
206
-
-
20044377802
-
Optimizing drug delivery systems using systematic "design of experiments." Part I: Fundamental aspects
-
Singh B, Kumar R, Ahuja N. Optimizing drug delivery systems using systematic "design of experiments." Part I: fundamental aspects. Crit Rev Ther Drug Carrier Syst. 2005;22(1):27-105.
-
(2005)
Crit Rev Ther Drug Carrier Syst.
, vol.22
, Issue.1
, pp. 27-105
-
-
Singh, B.1
Kumar, R.2
Ahuja, N.3
-
207
-
-
23844484653
-
Optimizing drug delivery systems using systematic "design of experiments." Part II: Retrospect and prospects
-
Singh B, Dahiya M, Saharan V, Ahuja N. Optimizing drug delivery systems using systematic "design of experiments." Part II: retrospect and prospects. Crit Rev Ther Drug Carrier Syst. 2005;22(3): 215-294
-
(2005)
Crit Rev Ther Drug Carrier Syst.
, vol.22
, Issue.3
, pp. 215-294
-
-
Singh, B.1
Dahiya, M.2
Saharan, V.3
Ahuja, N.4
-
208
-
-
51449124269
-
Exemestane loaded self-microemulsifying drug delivery system (SMEDDS): Development and optimization
-
Singh AK, Chaurasiya A, Singh M, Upadhyay SC, Mukherjee R, Khar RK. Exemestane loaded self-microemulsifying drug delivery system (SMEDDS): development and optimization. AAPS PharmSciTech. 2008;9(2):628-634
-
(2008)
AAPS PharmSciTech.
, vol.9
, Issue.2
, pp. 628-634
-
-
Singh, A.K.1
Chaurasiya, A.2
Singh, M.3
Upadhyay, S.C.4
Mukherjee, R.5
Khar, R.K.6
-
209
-
-
24744444477
-
Response surface methodology for the development of self-nanoemulsified drug delivery system (SNEDDS) of all-trans-retinol acetate
-
Taha EI, Samy AM, Kassem AA, Khan MA. Response surface methodology for the development of self-nanoemulsified drug delivery system (SNEDDS) of all-trans-retinol acetate. Pharm Dev Technol. 2005;10(3):363-370
-
(2005)
Pharm Dev Technol.
, vol.10
, Issue.3
, pp. 363-370
-
-
Taha, E.I.1
Samy, A.M.2
Kassem, A.A.3
Khan, M.A.4
-
210
-
-
23144438952
-
Response surface methodology for optimization and characterization of limonene-based coenzyme Q10 self-nanoemulsified capsule dosage form
-
Palamakula A, Nutan MT, Khan MA. Response surface methodology for optimization and characterization of limonene-based coenzyme Q10 self-nanoemulsified capsule dosage form. AAPS PharmSciTech. 2004;5(4):e66.
-
(2004)
AAPS PharmSciTech.
, vol.5
, Issue.4
-
-
Palamakula, A.1
Nutan, M.T.2
Khan, M.A.3
-
211
-
-
70449450409
-
Application of Box-Behnken design in understanding the quality of genistein self-nanoemulsified drug delivery systems and optimizing its formulation
-
Zhu S, Hong M, Liu C, Pei Y. Application of Box-Behnken design in understanding the quality of genistein self-nanoemulsified drug delivery systems and optimizing its formulation. Pharm Dev Technol. 2009;14(6):642-649
-
(2009)
Pharm Dev Technol.
, vol.14
, Issue.6
, pp. 642-649
-
-
Zhu, S.1
Hong, M.2
Liu, C.3
Pei, Y.4
-
212
-
-
23144432623
-
Effect of formulation variables on preparation and evaluation of gelled self-emulsifying drug delivery system (SEDDS) of ketoprofen
-
Patil P, Joshi P, Paradkar A. Effect of formulation variables on preparation and evaluation of gelled self-emulsifying drug delivery system (SEDDS) of ketoprofen. AAPS PharmSciTech. 2004;5(3):e42.
-
(2004)
AAPS PharmSciTech.
, vol.5
, Issue.3
-
-
Patil, P.1
Joshi, P.2
Paradkar, A.3
-
213
-
-
33749454734
-
Optimization of self-microemulsifying drug delivery systems (SMEDDS) using a D-optimal design and the desirability function
-
Holm R, Jensen IH, Sonnergaard J. Optimization of self-microemulsifying drug delivery systems (SMEDDS) using a D-optimal design and the desirability function. Drug Dev Ind Pharm. 2006;32(9):1025-1032
-
(2006)
Drug Dev Ind Pharm.
, vol.32
, Issue.9
, pp. 1025-1032
-
-
Holm, R.1
Jensen, I.H.2
Sonnergaard, J.3
-
214
-
-
4444273107
-
Application of a mixture experimental design in the optimization of a self-emulsifying formulation with a high drug load
-
Gao P, Witt MJ, Haskell RJ, Zamora KM, Shifflett JR. Application of a mixture experimental design in the optimization of a self-emulsifying formulation with a high drug load. Pharm Dev Technol. 2004;9(3): 301-309
-
(2004)
Pharm Dev Technol.
, vol.9
, Issue.3
, pp. 301-309
-
-
Gao, P.1
Witt, M.J.2
Haskell, R.J.3
Zamora, K.M.4
Shifflett, J.R.5
-
215
-
-
57049152323
-
Optimization and in situ intestinal absorption of self-microemulsifying drug delivery system of oridonin
-
Liu Y, Zhang P, Feng N, Zhang X, Wu S, Zhao J. Optimization and in situ intestinal absorption of self-microemulsifying drug delivery system of oridonin. Int J Pharm. 2009;365(1-2):136-142
-
(2009)
Int J Pharm.
, vol.365
, Issue.1-2
, pp. 136-142
-
-
Liu, Y.1
Zhang, P.2
Feng, N.3
Zhang, X.4
Wu, S.5
Zhao, J.6
-
216
-
-
34648812681
-
Application of mixture experimental design to simvastatin apparent solubility predictions in the microemulsifion formed by self-microemulsifying
-
Meng J, Zheng L. Application of mixture experimental design to simvastatin apparent solubility predictions in the microemulsifion formed by self-microemulsifying. Drug Dev Ind Pharm. 2007;33(9):927-931
-
(2007)
Drug Dev Ind Pharm.
, vol.33
, Issue.9
, pp. 927-931
-
-
Meng, J.1
Zheng, L.2
-
217
-
-
0141798535
-
Response surface methodology for the optimization of ubiquinone self-nanoemulsified drug delivery system
-
Nazzal S, Khan MA. Response surface methodology for the optimization of ubiquinone self-nanoemulsified drug delivery system. AAPS PharmSciTech. 2002;3(1):E3.
-
(2002)
AAPS PharmSciTech.
, vol.3
, Issue.1
-
-
Nazzal, S.1
Khan, M.A.2
-
218
-
-
0037142237
-
Optimization of a self-nanoemulsified tablet dosage form of Ubiquinone using response surface methodology: Effect of formulation ingredients
-
Nazzal S, Nutan M, Palamakula A, Shah R, Zaghloul AA and Khan MA. Optimization of a self-nanoemulsified tablet dosage form of Ubiquinone using response surface methodology: effect of formulation ingredients. Int J Pharm. 2002;240(1-2):103-114
-
(2002)
Int J Pharm.
, vol.240
, Issue.1-2
, pp. 103-114
-
-
Nazzal, S.1
Nutan, M.2
Palamakula, A.3
Shah, R.4
Zaghloul, A.A.5
Khan, M.A.6
-
219
-
-
33645468795
-
Porous polystyrene beads as carriers for selfemulsifying system containing loratadine
-
Patil P, Paradkar A. Porous polystyrene beads as carriers for selfemulsifying system containing loratadine. AAPS PharmSciTech. 2006;7(1):E28.
-
(2006)
AAPS PharmSciTech.
, vol.7
, Issue.1
-
-
Patil, P.1
Paradkar, A.2
-
220
-
-
33645020126
-
Light scattering measurements on microemulsions: Estimation of droplet sizes
-
Goddeeris C, Cuppo F, Reynaers H, Bouwman WG, Van den Mooter G. Light scattering measurements on microemulsions: estimation of droplet sizes. Int J Pharm. 2006;312(1-2):187-195
-
(2006)
Int J Pharm.
, vol.312
, Issue.1-2
, pp. 187-195
-
-
Goddeeris, C.1
Cuppo, F.2
Reynaers, H.3
Bouwman, W.G.4
Van Den Mooter, G.5
-
221
-
-
60749084743
-
A systematic dilution study of self-microemulsifying drug delivery systems in artificial intestinal fluid using dynamic laser light backscattering
-
Ditner C, Bravo R, Imanidis G, Kuentz M. A systematic dilution study of self-microemulsifying drug delivery systems in artificial intestinal fluid using dynamic laser light backscattering. Drug Dev Ind Pharm. 2009;35(2):199-208.
-
(2009)
Drug Dev Ind Pharm.
, vol.35
, Issue.2
, pp. 199-208
-
-
Ditner, C.1
Bravo, R.2
Imanidis, G.3
Kuentz, M.4
-
222
-
-
0026926486
-
CONTIN analysis of colloidal aggregates
-
Ju RTC, Frank CW, Gast AP. CONTIN analysis of colloidal aggregates. Langmuir. 1992;8(9):2165-2171
-
(1992)
Langmuir.
, vol.8
, Issue.9
, pp. 2165-2171
-
-
Ju, R.T.C.1
Frank, C.W.2
Gast, A.P.3
-
223
-
-
0032099078
-
-
Laia CAT, López-Cornejo P, Costa SMB, dOliveira J, Martinho JMG. Dynamic light scattering study of AOT microemulsions with nonaqueous polar additives in an oil continuous phase. Langmuir. 1998;14(13):3531-3537
-
(1998)
Martinho JMG. Dynamic Light Scattering Study of AOT Microemulsions with Nonaqueous Polar Additives in An Oil Continuous Phase. Langmuir
, vol.14
, Issue.13
, pp. 3531-3537
-
-
Laia, C.A.T.1
López-Cornejo, P.2
Costa, S.M.B.3
-
224
-
-
76849112546
-
Critical concentrations in the dilution of oral self-microemulsifying drug delivery systems
-
Oct 30. [Epub ahead of print]
-
Kuentz M, Cavegn M. Critical concentrations in the dilution of oral self-microemulsifying drug delivery systems. Drug Dev Ind Pharm. 2009 Oct 30. [Epub ahead of print]
-
(2009)
Drug Dev Ind Pharm.
-
-
Kuentz, M.1
Cavegn, M.2
-
225
-
-
34548567075
-
Structural development of self nano emulsifying drug delivery systems (SNEDDS) during in vitro lipid digestion monitored by small-angle x-ray scattering
-
Fatouros D, Deen G, Arleth L, Bergenstahl B, Nielsen F, Pedersen J, Mullertz A. structural development of self nano emulsifying drug delivery systems (SNEDDS) during in vitro lipid digestion monitored by small-angle x-ray scattering. Pharm Res. 2007;24(10):1844-1853
-
(2007)
Pharm Res.
, vol.24
, Issue.10
, pp. 1844-1853
-
-
Fatouros, D.1
Deen, G.2
Arleth, L.3
Bergenstahl, B.4
Nielsen, F.5
Pedersen, J.6
Mullertz, A.7
-
226
-
-
34548567075
-
Structural development of self nano emulsifying drug delivery systems (SNEDDS) during in vitro lipid digestion monitored by small-angle X-ray scattering
-
Fatouros DG, Deen GR, Arleth L, Bergenstahl B, Nielsen FS, Pedersen JS, Mullertz A. Structural development of self nano emulsifying drug delivery systems (SNEDDS) during in vitro lipid digestion monitored by small-angle X-ray scattering. Pharm Res. 2007;24(10):1844-1853
-
(2007)
Pharm Res.
, vol.24
, Issue.10
, pp. 1844-1853
-
-
Fatouros, D.G.1
Deen, G.R.2
Arleth, L.3
Bergenstahl, B.4
Nielsen, F.S.5
Pedersen, J.S.6
Mullertz, A.7
-
227
-
-
84979947632
-
Scanning electron microscopy and x-ray microanalysis
-
Goldstein GI, Newbury DE, Echlin P, Joy DC, Fiori C, Lifshin E. Scanning electron microscopy and x-ray microanalysis. New York: Plenum Press, 1981.
-
(1981)
New York: Plenum Press
-
-
Goldstein, G.I.1
Newbury, D.E.2
Echlin, P.3
Joy, D.C.4
Fiori, C.5
Lifshin, E.6
-
228
-
-
76849086436
-
Transmission electron microscopy: Physics of image formation
-
Reimer L, Kohl H. Transmission electron microscopy: physics of image formation. Berlin: Axel-Springer, 2008.
-
(2008)
Berlin: Axel-Springer
-
-
Reimer, L.1
Kohl, H.2
-
229
-
-
84888073048
-
Three-dimensional electron microscopy of macromolecular assemblies
-
Frank J. Three-dimensional electron microscopy of macromolecular assemblies. New York: Oxford University Press, 2006.
-
(2006)
New York: Oxford University Press
-
-
Frank, J.1
-
230
-
-
34247536339
-
Morphological observations on a lipid-based drug delivery system during in vitro digestion
-
Fatouros DG, Bergenstahl B, Mullertz A. Morphological observations on a lipid-based drug delivery system during in vitro digestion. Eur J Pharm Sci. 2007;31(2):85-94.
-
(2007)
Eur J Pharm Sci.
, vol.31
, Issue.2
, pp. 85-94
-
-
Fatouros, D.G.1
Bergenstahl, B.2
Mullertz, A.3
-
231
-
-
34547106058
-
Quality by design: Characterization of self-nano-emulsified drug delivery systems (SNEDDs) using ultrasonic resonator technology
-
Shah RB, Zidan AS, Funck T, Tawakkul MA, Nguyenpho A, Khan MA. Quality by design: characterization of self-nano-emulsified drug delivery systems (SNEDDs) using ultrasonic resonator technology. Int J Pharm. 2007;341(1-2):189-194
-
(2007)
Int J Pharm.
, vol.341
, Issue.1-2
, pp. 189-194
-
-
Shah, R.B.1
Zidan, A.S.2
Funck, T.3
Tawakkul, M.A.4
Nguyenpho, A.5
Khan, M.A.6
-
232
-
-
0017200358
-
Rheological characterisation of self-emulsifying oil/surfactant systems
-
Groves MJ, de Galindez DA. Rheological characterisation of self-emulsifying oil/surfactant systems. Acta Pharm Suec. 1976;13(4):353-360
-
(1976)
Acta Pharm Suec.
, vol.13
, Issue.4
, pp. 353-360
-
-
Groves, M.J.1
De Galindez, D.A.2
-
233
-
-
70349335526
-
Rheological investigation of selfemulsification process
-
Biradar SV, Dhumal RS, Paradkar A. Rheological investigation of selfemulsification process. J Pharm Pharm Sci. 2009;12(1):17-31.
-
(2009)
J Pharm Pharm Sci.
, vol.12
, Issue.1
, pp. 17-31
-
-
Biradar, S.V.1
Dhumal, R.S.2
Paradkar, A.3
-
234
-
-
23844471635
-
The rheological properties of self-emulsifying systems, water and microcrystalline cellulose
-
Newton JM, Bazzigialuppi M, Podczeck F, Booth S, Clarke A. The rheological properties of self-emulsifying systems, water and microcrystalline cellulose. Eur J Pharm Sci. 2005;26(2):176-183
-
(2005)
Eur J Pharm Sci.
, vol.26
, Issue.2
, pp. 176-183
-
-
Newton, J.M.1
Bazzigialuppi, M.2
Podczeck, F.3
Booth, S.4
Clarke, A.5
-
235
-
-
41849143050
-
Design and evaluation of prostaglandin E1 (PGE1) intraurethral liquid formulation employing self-microemulsifying drug delivery system (SMEDDS) for erectile dysfunction treatment
-
Lee S, Lee J, Choi YW. Design and evaluation of prostaglandin E1 (PGE1) intraurethral liquid formulation employing self-microemulsifying drug delivery system (SMEDDS) for erectile dysfunction treatment. Biol Pharm Bull. 2008;31(4):668-672
-
(2008)
Biol Pharm Bull.
, vol.31
, Issue.4
, pp. 668-672
-
-
Lee, S.1
Lee, J.2
Choi, Y.W.3
-
236
-
-
34247205833
-
Formulation development and optimization using nanoemulsion technique: A technical note
-
Shafiq-un-Nabi S, Shakeel F, Talegaonkar S, Ali J, Baboota S, Ahuja A, Khar RK, Ali M. Formulation development and optimization using nanoemulsion technique: a technical note. AAPS PharmSciTech. 2007;8(2):E1-E6.
-
(2007)
AAPS PharmSciTech.
, vol.8
, Issue.2
-
-
Shafiq-Un-Nabi, S.1
Shakeel, F.2
Talegaonkar, S.3
Ali, J.4
Baboota, S.5
Ahuja, A.6
Khar, R.K.7
Ali, M.8
-
237
-
-
44849087456
-
Design and evaluation of self-microemulsifying drug delivery system (SMEDDS) of tacrolimus
-
Borhade V, Nair H, Hegde D. Design and evaluation of self- microemulsifying drug delivery system (SMEDDS) of tacrolimus. AAPS PharmSciTech. 2008;9(1):13-21.
-
(2008)
AAPS PharmSciTech.
, vol.9
, Issue.1
, pp. 13-21
-
-
Borhade, V.1
Nair, H.2
Hegde, D.3
-
238
-
-
0035055279
-
Small-intestine absorption during continuous intraduodenal infusion of nutrients in dogs
-
Defilippi C, Cumsille F. Small-intestine absorption during continuous intraduodenal infusion of nutrients in dogs. Nutrition. 2001;17(3):254-8
-
(2001)
Nutrition
, vol.17
, Issue.3
, pp. 254-258
-
-
Defilippi, C.1
Cumsille, F.2
-
239
-
-
0345275777
-
The small intestine as a xenobiotic-metabolizing organ
-
238. Kaminsky LS, Zhang QY. The small intestine as a xenobiotic- metabolizing organ. Drug Metab Dispos. 2003;31(12):1520-1525
-
(2003)
Drug Metab Dispos.
, vol.31
, Issue.12
, pp. 1520-1525
-
-
Kaminsky, L.S.1
Zhang, Q.Y.2
-
240
-
-
0033278620
-
Gastrointestinal absorption of drugs: Methods and studies
-
Barthe L, Woodley J, Houin G. Gastrointestinal absorption of drugs: methods and studies. Fundam Clin Pharmacol. 1999;13(2):154-168
-
(1999)
Fundam Clin Pharmacol.
, vol.13
, Issue.2
, pp. 154-168
-
-
Barthe, L.1
Woodley, J.2
Houin, G.3
-
241
-
-
0029972886
-
Estimation of oral drug absorption in man based on intestine permeability in rats
-
Levet-Trafit B, Gruyer MS, Marjanovic M, Chou RC. Estimation of oral drug absorption in man based on intestine permeability in rats. Life Sci. 1996;58(24):PL359-63.
-
(1996)
Life Sci.
, vol.58
, pp. 24
-
-
Levet-Trafit, B.1
Gruyer, M.S.2
Marjanovic, M.3
Chou, R.C.4
-
242
-
-
27744605985
-
-
Sharma P, Varma MV, Chawla HP, Panchagnula R. In situ and in vivo efficacy of peroral absorption enhancers in rats and correlation to in vitro mechanistic studies. Farmaco. 2005;60(11-12):874-883
-
(2005)
In Situ and in Vivo Efficacy of Peroral Absorption Enhancers in Rats and Correlation to in Vitro Mechanistic Studies. Farmaco.
, vol.60
, Issue.11-12
, pp. 874-883
-
-
Sharma, P.1
Varma, M.V.2
Chawla, H.P.3
Panchagnula, R.4
-
243
-
-
39549101971
-
Application of rat in situ single-pass intestinal perfusion in the evaluation of presystemic extraction of indinavir under different perfusion rates
-
Ho YF, Lai MY, Yu HY, Huang DK, Hsueh WC, Tsai TH, Lin CC. Application of rat in situ single-pass intestinal perfusion in the evaluation of presystemic extraction of indinavir under different perfusion rates. J Formos Med Assoc. 2008;107(1):37-45.
-
(2008)
J Formos Med Assoc.
, vol.107
, Issue.1
, pp. 37-45
-
-
Ho, Y.F.1
Lai, M.Y.2
Yu, H.Y.3
Huang, D.K.4
Hsueh, W.C.5
Tsai, T.H.6
Lin, C.C.7
-
244
-
-
31144465037
-
Effect of intestinal fluid flux on ibuprofen absorption in the rat intestine
-
Lane ME, Levis KA, Corrigan OI. Effect of intestinal fluid flux on ibuprofen absorption in the rat intestine. Int J Pharm. 2006;309(1-2): 60-66
-
(2006)
Int J Pharm.
, vol.309
, Issue.1-2
, pp. 60-66
-
-
Lane, M.E.1
Levis, K.A.2
Corrigan, O.I.3
-
245
-
-
0031659639
-
An improved everted gut sac as a simple and accurate technique to measure paracellular transport across the small intestine
-
Barthe L, Woodley JF, Kenworthy S, Houin G. An improved everted gut sac as a simple and accurate technique to measure paracellular transport across the small intestine. Eur J Drug Metab Pharmacokinet. 1998;23(2):313-323
-
(1998)
Eur J Drug Metab Pharmacokinet.
, vol.23
, Issue.2
, pp. 313-323
-
-
Barthe, L.1
Woodley, J.F.2
Kenworthy, S.3
Houin, G.4
-
246
-
-
0028243664
-
Use of everted intestinal rings for in vitro examination of oral absorption potential
-
Leppert PS, Fix JA. Use of everted intestinal rings for in vitro examination of oral absorption potential. J Pharm Sci. 1994;83(7):976-981
-
(1994)
J Pharm Sci.
, vol.83
, Issue.7
, pp. 976-981
-
-
Leppert, P.S.1
Fix, J.A.2
-
247
-
-
0017683008
-
Everted rat intestinal sacs as an in vitro model for assessing absorptivity of new drugs
-
Chowhan ZT, Amaro AA. Everted rat intestinal sacs as an in vitro model for assessing absorptivity of new drugs. J Pharm Sci. 1977;66(9): 1249-1253
-
(1977)
J Pharm Sci.
, vol.66
, Issue.9
, pp. 1249-1253
-
-
Chowhan, Z.T.1
Amaro, A.A.2
-
248
-
-
76849115805
-
Impact of emulsion-based drug delivery systems on intestinal permeability and drug release kinetics
-
Oct 20. [Epub ahead of print]
-
Buyukozturk F, Benneyan JC, Carrier RL. Impact of emulsion-based drug delivery systems on intestinal permeability and drug release kinetics. J Control Release. 2009 Oct 20. [Epub ahead of print]
-
(2009)
J Control Release
-
-
Buyukozturk, F.1
Benneyan, J.C.2
Carrier, R.L.3
-
249
-
-
0022351065
-
In vitro drug absorption models. I. Brush border membrane vesicles, isolated mucosal cells and everted intestinal rings: Characterization and salicylate accumulation
-
Osiecka I, Porter PA, Borchardt RT, Fix JA, Gardner CR. In vitro drug absorption models. I. Brush border membrane vesicles, isolated mucosal cells and everted intestinal rings: characterization and salicylate accumulation. Pharm Res. 1985;2(10):284-293
-
(1985)
Pharm Res.
, vol.2
, Issue.10
, pp. 284-293
-
-
Osiecka, I.1
Porter, P.A.2
Borchardt, R.T.3
Fix, J.A.4
Gardner, C.R.5
-
250
-
-
84934435626
-
In vitro systems for studying epithelial transport of macromolecules
-
Daum N, Neumeyer A, Wahl B, Bur M, Lehr CM. In vitro systems for studying epithelial transport of macromolecules. Methods Mol Biol. 2009;480:151-164
-
(2009)
Methods Mol Biol.
, vol.480
, pp. 151-164
-
-
Daum, N.1
Neumeyer, A.2
Wahl, B.3
Bur, M.4
Lehr, C.M.5
-
251
-
-
0018361195
-
Method of preparing isolated colonic epithelial cells (colonocytes) for metabolic studies
-
Roediger WE, Truelove SC. Method of preparing isolated colonic epithelial cells (colonocytes) for metabolic studies. Gut. 1979;20(6):484-488
-
(1979)
Gut.
, vol.20
, Issue.6
, pp. 484-488
-
-
Roediger, W.E.1
Truelove, S.C.2
-
252
-
-
0019351130
-
Isolation and characterization of epithelial cell types from the normal rat colon
-
Chopra DP, Yeh K, Brockman RW. Isolation and characterization of epithelial cell types from the normal rat colon. Cancer Res. 1981;41(1):168-175 (Pubitemid 11218812)
-
(1981)
Cancer Research
, vol.41
, Issue.1
, pp. 168-175
-
-
Chopra, D.P.1
Yeh, K.2
Brockman, R.W.3
-
253
-
-
0023269297
-
Synthesis of glycosaminoglycans by undifferentiated and differentiated HT29 human colonic cancer cells
-
Simon-Assmann P, Bouziges F, Daviaud D, Haffen K, Kedinger M. Synthesis of glycosaminoglycans by undifferentiated and differentiated HT29 human colonic cancer cells. Cancer Res. 1987;47(16):4478-4484
-
(1987)
Cancer Res.
, vol.47
, Issue.16
, pp. 4478-4484
-
-
Simon-Assmann, P.1
Bouziges, F.2
Daviaud, D.3
Haffen, K.4
Kedinger, M.5
-
254
-
-
0000569766
-
Established kidney cell lines of normal adult bovine and ovine origin
-
Madin SH, Darby NB, Jr. Established kidney cell lines of normal adult bovine and ovine origin. Proc Soc Exp Biol Med. 1958;98(3):574-576
-
(1958)
Proc Soc Exp Biol Med.
, vol.98
, Issue.3
, pp. 574-576
-
-
Madin, S.H.1
Darby Jr., N.B.2
-
255
-
-
24944564503
-
The in vitro cultivation of tissues of domestic and laboratory animals
-
Madin SH, Andriese PC, Darby NB. The in vitro cultivation of tissues of domestic and laboratory animals. Am J Vet Res. 1957;18(69):932-941
-
(1957)
Am J Vet Res.
, vol.18
, Issue.69
, pp. 932-941
-
-
Madin, S.H.1
Andriese, P.C.2
Darby, N.B.3
-
256
-
-
49049113267
-
Advances in the MDCK-MDR1 cell model and its applications to screen drug permeability
-
Liu Y, Zeng S. Advances in the MDCK-MDR1 cell model and its applications to screen drug permeability. Yao Xue Xue Bao. 2008;43(6):559-564
-
(2008)
Yao Xue Xue Bao.
, vol.43
, Issue.6
, pp. 559-564
-
-
Liu, Y.1
Zeng, S.2
-
257
-
-
0030845195
-
Low permeabilities of MDCK cell monolayers: A model barrier epithelium
-
Pt 2
-
Lavelle JP, Negrete HO, Poland PA, Kinlough CL, Meyers SD, Hughey RP, Zeidel ML. Low permeabilities of MDCK cell monolayers: a model barrier epithelium. Am J Physiol. 1997;273(1 Pt 2):F67-75.
-
(1997)
Am J Physiol.
, vol.273
, Issue.1
-
-
Lavelle, J.P.1
Negrete, H.O.2
Poland, P.A.3
Kinlough, C.L.4
Meyers, S.D.5
Hughey, R.P.6
Zeidel, M.L.7
-
258
-
-
70449109156
-
Remodeling of the tight junction during recovery from exposure to hydrogen peroxide in kidney epithelial cells
-
Gonzalez JE, Digeronimo RJ, Arthur DE, King JM. Remodeling of the tight junction during recovery from exposure to hydrogen peroxide in kidney epithelial cells. Free Radic Biol Med. 2009.
-
(2009)
Free Radic Biol Med.
-
-
Gonzalez, J.E.1
Digeronimo, R.J.2
Arthur, D.E.3
King, J.M.4
-
259
-
-
0028948839
-
A theoretical basis for a biopharmaceutic drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability
-
Amidon GL, Lennernas H, Shah VP, Crison JR. A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm Res. 1995;12(3):413-420
-
(1995)
Pharm Res.
, vol.12
, Issue.3
, pp. 413-420
-
-
Amidon, G.L.1
Lennernas, H.2
Shah, V.P.3
Crison, J.R.4
-
263
-
-
37849030370
-
Dissolution enhancement of fenofibrate by micronization, cogrinding and spray-drying: Comparison with commercial preparations
-
Vogt M, Kunath K, Dressman JB. Dissolution enhancement of fenofibrate by micronization, cogrinding and spray-drying: comparison with commercial preparations. Eur J Pharm Biopharm. 2008;68(2):283-288
-
(2008)
Eur J Pharm Biopharm.
, vol.68
, Issue.2
, pp. 283-288
-
-
Vogt, M.1
Kunath, K.2
Dressman, J.B.3
-
264
-
-
67349277384
-
Solubility-enhanced electrokinetic movement of hexachlorobenzene in sediments: A comparison of cosolvent and cyclodextrin
-
Wan J, Yuan S, Chen J, Li T, Lin L, Lu X. Solubility-enhanced electrokinetic movement of hexachlorobenzene in sediments: a comparison of cosolvent and cyclodextrin. J Hazard Mater. 2009;166(1):221-226
-
(2009)
J Hazard Mater.
, vol.166
, Issue.1
, pp. 221-226
-
-
Wan, J.1
Yuan, S.2
Chen, J.3
Li, T.4
Lin, L.5
Lu, X.6
-
265
-
-
0026785430
-
Solubilization and dissolution properties of a leukotriene-D4 antagonist in micellar solutions
-
Kararli TT, Gupta VW. Solubilization and dissolution properties of a leukotriene-D4 antagonist in micellar solutions. J Pharm Sci. 1992;81(5):483-485
-
(1992)
J Pharm Sci.
, vol.81
, Issue.5
, pp. 483-485
-
-
Kararli, T.T.1
Gupta, V.W.2
-
266
-
-
68349157666
-
Strongly enhanced dissolution rate of fenofibrate solid dispersion tablets by incorporation of superdisintegrants
-
Srinarong P, Faber JH, Visser MR, Hinrichs WL, Frijlink HW. Strongly enhanced dissolution rate of fenofibrate solid dispersion tablets by incorporation of superdisintegrants. Eur J Pharm Biopharm. 2009;73(1):154-161
-
(2009)
Eur J Pharm Biopharm.
, vol.73
, Issue.1
, pp. 154-161
-
-
Srinarong, P.1
Faber, J.H.2
Visser, M.R.3
Hinrichs, W.L.4
Frijlink, H.W.5
-
267
-
-
70350668808
-
Dissolution rate enhancement of the poorly water-soluble drug Tibolone using PVP SiO2 and their nanocomposites as appropriate drug carriers
-
Papadimitriou S, Bikiaris D. Dissolution rate enhancement of the poorly water-soluble drug Tibolone using PVP, SiO2, and their nanocomposites as appropriate drug carriers. Drug Dev Ind Pharm. 2009;35(9):1128-1138
-
(2009)
Drug Dev Ind Pharm.
, vol.35
, Issue.9
, pp. 1128-1138
-
-
Papadimitriou, S.1
Bikiaris, D.2
-
268
-
-
48149100781
-
Vitro-in vivo correlations of self-emulsifying drug delivery systems combining the dynamic lipolysis model and neuro-fuzzy networks
-
Fatouros DG, Nielsen FS, Douroumis D, Hadjileontiadis LJ, Mullertz A. In vitro-in vivo correlations of self-emulsifying drug delivery systems combining the dynamic lipolysis model and neuro-fuzzy networks. Eur J Pharm Biopharm. 2008;69(3):887-898
-
(2008)
Eur J Pharm Biopharm.
, vol.69
, Issue.3
, pp. 887-898
-
-
Fatouros, D.G.1
Nielsen, F.S.2
Douroumis, D.3
Hadjileontiadis, L.J.4
Mullertz, A.5
-
270
-
-
0035478436
-
In vitro assessment of oral lipid based formulations
-
Porter CJ, Charman WN. In vitro assessment of oral lipid based formulations. Adv Drug Deliv Rev. 2001;50(Suppl 1):S127-47.
-
(2001)
Adv Drug Deliv Rev.
, vol.50
, Issue.SUPPL 1
-
-
Porter, C.J.1
Charman, W.N.2
-
271
-
-
0025264030
-
Physical-chemical behavior of dietary and biliary lipids during intestinal digestion and absorption
-
Hernell O, Staggers JE, Carey MC. Physical-chemical behavior of dietary and biliary lipids during intestinal digestion and absorption. Biochemistry. 1990;29(8):2041-2056
-
(1990)
Biochemistry
, vol.29
, Issue.8
, pp. 2041-2056
-
-
Hernell, O.1
Staggers, J.E.2
Carey, M.C.3
-
272
-
-
0024244050
-
Uptake of fatty acids by jejunal mucosal cells is mediated by a fatty acid binding membrane protein
-
Stremmel W. Uptake of fatty acids by jejunal mucosal cells is mediated by a fatty acid binding membrane protein. J Clin Invest. 1988;82(6):2001-2010
-
(1988)
J Clin Invest.
, vol.82
, Issue.6
, pp. 2001-2010
-
-
Stremmel, W.1
-
273
-
-
0343408485
-
Lipophilic prodrugs designed for intestinal lymphatic transport
-
Charman WN, Porter CJH. Lipophilic prodrugs designed for intestinal lymphatic transport. Adv Drug Deliv Rev. 1996;19(2):149-169
-
(1996)
Adv Drug Deliv Rev.
, vol.19
, Issue.2
, pp. 149-169
-
-
Charman, W.N.1
Porter, C.J.H.2
-
274
-
-
0017069413
-
The structure of lymphatic capillaries in lymph formation
-
Leak LV. The structure of lymphatic capillaries in lymph formation. Fed Proc. 1976;35(8):1863-1871
-
(1976)
Fed Proc.
, vol.35
, Issue.8
, pp. 1863-1871
-
-
Leak, L.V.1
-
275
-
-
39149108776
-
Lipid-based delivery systems and intestinal lymphatic drug transport: A mechanistic update
-
Trevaskis NL, Charman WN, Porter CJH. Lipid-based delivery systems and intestinal lymphatic drug transport: a mechanistic update. Adv Drug Deliv Rev. 2008;60(6):702-716
-
(2008)
Adv Drug Deliv Rev.
, vol.60
, Issue.6
, pp. 702-716
-
-
Trevaskis, N.L.1
Charman, W.N.2
Porter, C.J.H.3
-
276
-
-
0035984949
-
Lipid-based formulations for intestinal lymphatic delivery
-
ODriscoll CM. Lipid-based formulations for intestinal lymphatic delivery. Eur J Pharm Sci. 2002;15(5):405-415
-
(2002)
Eur J Pharm Sci.
, vol.15
, Issue.5
, pp. 405-415
-
-
Odriscoll, C.M.1
-
277
-
-
0035940071
-
The physiology of the lymphatic system
-
Swartz MA. The physiology of the lymphatic system. Adv Drug Deliv Rev. 2001;50(1-2):3-20.
-
(2001)
Adv Drug Deliv Rev.
, vol.50
, Issue.1-2
, pp. 3-20
-
-
Swartz, M.A.1
-
278
-
-
0035940059
-
Recent advances in the understanding of uptake of microparticulates across the gastrointestinal lymphatics
-
Hussain N, Jaitley V, Florence AT. Recent advances in the understanding of uptake of microparticulates across the gastrointestinal lymphatics. Adv Drug Deliv Rev. 2001;50(1-2):107-142
-
(2001)
Adv Drug Deliv Rev.
, vol.50
, Issue.1-2
, pp. 107-142
-
-
Hussain, N.1
Jaitley, V.2
Florence, A.T.3
-
279
-
-
34247638077
-
Comparative study on digestive lipase activities on the self emulsifying excipient Labrasol, medium chain glycerides and PEG esters
-
Fernandez S, Jannin V, Rodier JD, Ritter N, Mahler B, Carriere F. Comparative study on digestive lipase activities on the self emulsifying excipient Labrasol, medium chain glycerides and PEG esters. Biochim Biophys Acta. 2007;1771(5):633-640
-
(2007)
Biochim Biophys Acta.
, vol.1771
, Issue.5
, pp. 633-640
-
-
Fernandez, S.1
Jannin, V.2
Rodier, J.D.3
Ritter, N.4
Mahler, B.5
Carriere, F.6
-
280
-
-
33847260132
-
A new standardized lipolysis approach for characterization of emulsions and dispersions
-
Brogard M, Troedsson E, Thuresson K, Ljusberg-Wahren H. A new standardized lipolysis approach for characterization of emulsions and dispersions. J Colloid Interface Sci. 2007;308(2):500-507
-
(2007)
J Colloid Interface Sci.
, vol.308
, Issue.2
, pp. 500-507
-
-
Brogard, M.1
Troedsson, E.2
Thuresson, K.3
Ljusberg-Wahren, H.4
-
281
-
-
0025239461
-
-
Staggers JE, Hernell O, Stafford RJ, Carey MC. Physical-chemical behavior of dietary and biliary lipids during intestinal digestion and absorption. 1. Phase behavior and aggregation states of model lipid systems patterned after aqueous duodenal contents of healthy adult human beings. Biochemistry. 1990;29(8):2028-2040
-
(1990)
Physical-chemical Behavior of Dietary and Biliary Lipids during Intestinal Digestion and Absorption
, vol.1
, Issue.29
, pp. 2028-2040
-
-
Staggers, J.E.1
Hernell, O.2
Stafford, R.J.3
Carey, M.C.4
-
283
-
-
0033818432
-
Effect of short-, medium-, and long-chain fatty acid-based vehicles on the absolute oral bioavailability and intestinal lymphatic transport of halofantrine and assessment of mass balance in lymph-cannulated and non-cannulated rats
-
Caliph SM, Charman WN, Porter CJ. Effect of short-, medium-, and long-chain fatty acid-based vehicles on the absolute oral bioavailability and intestinal lymphatic transport of halofantrine and assessment of mass balance in lymph-cannulated and non-cannulated rats. J Pharm Sci. 2000;89(8):1073-1084
-
(2000)
J Pharm Sci.
, vol.89
, Issue.8
, pp. 1073-1084
-
-
Caliph, S.M.1
Charman, W.N.2
Porter, C.J.3
-
284
-
-
0019413849
-
Bifunctional delivery system for selective transfer of bleomycin into lymphatics via enteral route
-
Hiroshi Y, Shozo M, Chiharu K, Hitoshi S. Bifunctional delivery system for selective transfer of bleomycin into lymphatics via enteral route. Int J Pharm. 1981;8(4):291-302.
-
(1981)
Int J Pharm.
, vol.8
, Issue.4
, pp. 291-302
-
-
Hiroshi, Y.1
Shozo, M.2
Chiharu, K.3
Hitoshi, S.4
-
285
-
-
0029379703
-
Targeting of colloids to lymph nodes: Influence of lymphatic physiology and colloidal characteristics
-
Hawley AE, Davis SS, Illum L. Targeting of colloids to lymph nodes: influence of lymphatic physiology and colloidal characteristics. Adv Drug Deliv Rev. 1995;17(1):129-48
-
(1995)
Adv Drug Deliv Rev.
, vol.17
, Issue.1
, pp. 129-148
-
-
Hawley, A.E.1
Davis, S.S.2
Illum, L.3
-
286
-
-
70449528399
-
Formulateability of ten compounds with different physicochemical profiles in SMEDDS
-
Thi TD, Van Speybroeck M, Barillaro V, Martens J, Annaert P, Augustijns P, Van Humbeeck J, Vermant J, Van den Mooter G. Formulateability of ten compounds with different physicochemical profiles in SMEDDS. Eur J Pharm Sci. 2009;38(5):479-88.
-
(2009)
Eur J Pharm Sci.
, vol.38
, Issue.5
, pp. 479-488
-
-
Thi, T.D.1
Van Speybroeck, M.2
Barillaro, V.3
Martens, J.4
Annaert, P.5
Augustijns, P.6
Van Humbeeck, J.7
Vermant, J.8
Van Den Mooter, G.9
-
287
-
-
0032714228
-
Inhibition of P-glycoprotein by D-alphatocopheryl polyethylene glycol 1000 succinate (TPGS)
-
Dintaman JM, Silverman JA. Inhibition of P-glycoprotein by D-alphatocopheryl polyethylene glycol 1000 succinate (TPGS). Pharm Res. 1999;16(10):1550-6
-
(1999)
Pharm Res.
, vol.16
, Issue.10
, pp. 1550-1556
-
-
Dintaman, J.M.1
Silverman, J.A.2
-
288
-
-
0027363774
-
Reversal of C1300 murine neuroblastoma multidrug resistance by cremophorEL, a solvent for cyclosporin A
-
Chervinsky DS, Brecher ML, Baker RM, Hoelcle MJ, Tebbi CK. Reversal of C1300 murine neuroblastoma multidrug resistance by cremophorEL, a solvent for cyclosporin A. Cancer Biother. 1993;8(1):67-75
-
(1993)
Cancer Biother.
, vol.8
, Issue.1
, pp. 67-75
-
-
Chervinsky, D.S.1
Brecher, M.L.2
Baker, R.M.3
Hoelcle, M.J.4
Tebbi, C.K.5
-
289
-
-
33749057113
-
Design and development of microemulsion drug delivery system of acyclovir for improvement of oral bioavailability
-
Ghosh PK, Majithiya RJ, Umrethia ML, Murthy RS. Design and development of microemulsion drug delivery system of acyclovir for improvement of oral bioavailability. AAPS PharmSciTech. 2006;7(3):77
-
(2006)
AAPS PharmSciTech.
, vol.7
, Issue.3
, pp. 77
-
-
Ghosh, P.K.1
Majithiya, R.J.2
Umrethia, M.L.3
Murthy, R.S.4
-
290
-
-
33750292120
-
HPLC determination of anethole trithione and its application to pharmacokinetics in rabbits
-
Jing Q, Shen Y, Ren F, Chen J, Jiang Z, Peng B, Leng Y, Dong J. HPLC determination of anethole trithione and its application to pharmacokinetics in rabbits. J Pharm Biomed Anal. 2006;42(5):613-7
-
(2006)
J Pharm Biomed Anal.
, vol.42
, Issue.5
, pp. 613-617
-
-
Jing, Q.1
Shen, Y.2
Ren, F.3
Chen, J.4
Jiang, Z.5
Peng, B.6
Leng, Y.7
Dong, J.8
-
291
-
-
0042168660
-
Oral bioavailability of the antioxidant astaxanthin in humans is enhanced by incorporation of lipid based formulations
-
Mercke Odeberg J, Lignell A, Pettersson A, Hoglund P. Oral bioavailability of the antioxidant astaxanthin in humans is enhanced by incorporation of lipid based formulations. Eur J Pharm Sci. 2003;19(4):299-304
-
(2003)
Eur J Pharm Sci.
, vol.19
, Issue.4
, pp. 299-304
-
-
Mercke Odeberg, J.1
Lignell, A.2
Pettersson, A.3
Hoglund, P.4
-
292
-
-
29744439280
-
Preparation and evaluation of selfmicroemulsifying drug delivery systems containing atorvastatin
-
Shen HR, Li ZD, Zhong MK. Preparation and evaluation of selfmicroemulsifying drug delivery systems containing atorvastatin. Yao Xue Xue Bao. 2005;40(11):982-7
-
(2005)
Yao Xue Xue Bao.
, vol.40
, Issue.11
, pp. 982-987
-
-
Shen, H.R.1
Li, Z.D.2
Zhong, M.K.3
-
293
-
-
64149103691
-
High performance liquid chromatography method for the pharmacokinetic study of bicalutamide SMEDDS and suspension formulations after oral administration to rats
-
Singh AK, Chaurasiya A, Jain GK, Awasthi A, Asati D, Mishra G, Khar RK, Mukherjee R. High performance liquid chromatography method for the pharmacokinetic study of bicalutamide SMEDDS and suspension formulations after oral administration to rats. Talanta. 2009;78(4-5):1310-4
-
(2009)
Talanta.
, vol.78
, Issue.4-5
, pp. 1310-1314
-
-
Singh, A.K.1
Chaurasiya, A.2
Jain, G.K.3
Awasthi, A.4
Asati, D.5
Mishra, G.6
Khar, R.K.7
Mukherjee, R.8
-
294
-
-
34648814989
-
Investigations of a novel self-emulsifying osmotic pump tablet containing carvedilol
-
Wei L, Li J, Guo L, Nie S, Pan W, Sun P, Liu H. Investigations of a novel self-emulsifying osmotic pump tablet containing carvedilol. Drug Dev Ind Pharm. 2007;33(9):990-8
-
(2007)
Drug Dev Ind Pharm.
, vol.33
, Issue.9
, pp. 990-998
-
-
Wei, L.1
Li, J.2
Guo, L.3
Nie, S.4
Pan, W.5
Sun, P.6
Liu, H.7
-
295
-
-
57349084177
-
Formulation and in vivo evaluation of chlorpropham (CIPC) oral formulations
-
Kuehl PJ, Brenner T, Jain PK, Karlage K, Sepassi K, Yang G, Mayersohn M, Yalkowsky SH, Myrdal PB. Formulation and in vivo evaluation of chlorpropham (CIPC) oral formulations. J Pharm Sci. 2008;97(12):5222-8
-
(2008)
J Pharm Sci.
, vol.97
, Issue.12
, pp. 5222-5228
-
-
Kuehl, P.J.1
Brenner, T.2
Jain, P.K.3
Karlage, K.4
Sepassi, K.5
Yang, G.6
Mayersohn, M.7
Yalkowsky, S.H.8
Myrdal, P.B.9
-
296
-
-
0030572634
-
Evaluation of emulsifiable glasses for the oral administration of cyclosporin in beagle dogs
-
Porter CJH, Charman SA, Williams RD, Bakalova MV, Charman WN. Evaluation of emulsifiable glasses for the oral administration of cyclosporin in beagle dogs. Int J Pharm. 1996;141(1-2):227-37
-
(1996)
Int J Pharm.
, vol.141
, Issue.1-2
, pp. 227-237
-
-
Porter, C.J.H.1
Charman, S.A.2
Williams, R.D.3
Bakalova, M.V.4
Charman, W.N.5
-
297
-
-
4344578729
-
Susceptibility to lipase-mediated digestion reduces the oral bioavailability of danazol after administration as a medium-chain lipid-based microemulsion formulation
-
Porter CJ, Kaukonen AM, Boyd BJ, Edwards GA, Charman WN. Susceptibility to lipase-mediated digestion reduces the oral bioavailability of danazol after administration as a medium-chain lipid-based microemulsion formulation. Pharm Res. 2004;21(8):1405-12
-
(2004)
Pharm Res.
, vol.21
, Issue.8
, pp. 1405-1412
-
-
Porter, C.J.1
Kaukonen, A.M.2
Boyd, B.J.3
Edwards, G.A.4
Charman, W.N.5
-
298
-
-
39149091886
-
Evaluation of the impact of surfactant digestion on the bioavailability of danazol after oral administration of lipidic selfemulsifying formulations to dogs
-
Cuine JF, McEvoy CL, Charman WN, Pouton CW, Edwards GA, Benameur H, Porter CJ. Evaluation of the impact of surfactant digestion on the bioavailability of danazol after oral administration of lipidic selfemulsifying formulations to dogs. J Pharm Sci. 2008;97(2):995-1012
-
(2008)
J Pharm Sci.
, vol.97
, Issue.2
, pp. 995-1012
-
-
Cuine, J.F.1
McEvoy, C.L.2
Charman, W.N.3
Pouton, C.W.4
Edwards, G.A.5
Benameur, H.6
Porter, C.J.7
-
299
-
-
33746006873
-
The novel formulation design of selfemulsifying drug delivery systems (SEDDS) type O/W microemulsion II: Stable gastrointestinal absorption of a poorly water soluble new compound, ER-1258 in bile-fistula rats
-
Araya H, Tomita M, Hayashi M. The novel formulation design of selfemulsifying drug delivery systems (SEDDS) type O/W microemulsion II: stable gastrointestinal absorption of a poorly water soluble new compound, ER-1258 in bile-fistula rats. Drug Metab Pharmacokinet. 2005;20(4):257-67
-
(2005)
Drug Metab Pharmacokinet.
, vol.20
, Issue.4
, pp. 257-267
-
-
Araya, H.1
Tomita, M.2
Hayashi, M.3
-
300
-
-
33745976753
-
The novel formulation design of self-emulsifying drug delivery systems (SEDDS) type O/W microemulsion I: Enhancing effects on oral bioavailability of poorly water soluble compounds in rats and beagle dogs
-
Araya H, Nagao S, Tomita M, Hayashi M. The novel formulation design of self-emulsifying drug delivery systems (SEDDS) type O/W microemulsion I: enhancing effects on oral bioavailability of poorly water soluble compounds in rats and beagle dogs. Drug Metab Pharmacokinet. 2005;20(4):244-56
-
(2005)
Drug Metab Pharmacokinet.
, vol.20
, Issue.4
, pp. 244-256
-
-
Araya, H.1
Nagao, S.2
Tomita, M.3
Hayashi, M.4
-
301
-
-
70449526521
-
Oral bioavailability enhancement of exemestane from self-microemulsifying drug delivery system (SMEDDS)
-
Singh AK, Chaurasiya A, Awasthi A, Mishra G, Asati D, Khar RK, Mukherjee R. Oral bioavailability enhancement of exemestane from self-microemulsifying drug delivery system (SMEDDS). AAPS PharmSciTech. 2009;10(3):906-16
-
(2009)
AAPS PharmSciTech.
, vol.10
, Issue.3
, pp. 906-916
-
-
Singh, A.K.1
Chaurasiya, A.2
Awasthi, A.3
Mishra, G.4
Asati, D.5
Khar, R.K.6
Mukherjee, R.7
-
302
-
-
41349115243
-
A high-throughput approach towards a novel formulation of fenofibrate in omega-3 oil
-
Ratanabanangkoon P, Guzman H, Almarsson O, Berkovitz D, Tokarcyzk S, Straughn AB, Chen H. A high-throughput approach towards a novel formulation of fenofibrate in omega-3 oil. Eur J Pharm Sci. 2008;33(4-5):351-60
-
(2008)
Eur J Pharm Sci.
, vol.33
, Issue.4-5
, pp. 351-360
-
-
Ratanabanangkoon, P.1
Guzman, H.2
Almarsson, O.3
Berkovitz, D.4
Tokarcyzk, S.5
Straughn, A.B.6
Chen, H.7
-
303
-
-
0032103706
-
Formulation design and bioavailability assessment of lipidic selfemulsifying formulations of halofantrine
-
Khoo S-M, Humberstone AJ, Porter CJH, Edwards GA, Charman WN. Formulation design and bioavailability assessment of lipidic selfemulsifying formulations of halofantrine. Int J Pharm. 1998;167(1-2):155-64
-
(1998)
Int J Pharm.
, vol.167
, Issue.1-2
, pp. 155-164
-
-
Khoo, S.-M.1
Humberstone, A.J.2
Porter, C.J.H.3
Edwards, G.A.4
Charman, W.N.5
-
304
-
-
33748960636
-
In vitro and in vivo evaluation of a novel oral insulin formulation
-
Ma EL, Ma H, Liu Z, Zheng GX, Duan MX. In vitro and in vivo evaluation of a novel oral insulin formulation. Acta Pharmacol Sin. 2006;27(10):1382-8
-
(2006)
Acta Pharmacol Sin.
, vol.27
, Issue.10
, pp. 1382-1388
-
-
Ma, E.L.1
Ma, H.2
Liu, Z.3
Zheng, G.X.4
Duan, M.X.5
-
305
-
-
34249690584
-
In vitro and in vivo comparative study of itraconazole bioavailability when formulated in highly soluble selfemulsifying system and in solid dispersion
-
Park MJ, Ren S, Lee BJ. In vitro and in vivo comparative study of itraconazole bioavailability when formulated in highly soluble selfemulsifying system and in solid dispersion. Biopharm Drug Dispos. 2007;28(4):199-207
-
(2007)
Biopharm Drug Dispos.
, vol.28
, Issue.4
, pp. 199-207
-
-
Park, M.J.1
Ren, S.2
Lee, B.J.3
-
306
-
-
38749146264
-
Reduced food-effect and enhanced bioavailability of a self-microemulsifying formulation of itraconazole in healthy volunteers
-
Woo JS, Song Y-K, Hong J-Y, Lim S-J, Kim C-K. Reduced food-effect and enhanced bioavailability of a self-microemulsifying formulation of itraconazole in healthy volunteers. Eur J Pharm Sci. 2008;33(2):159-65
-
(2008)
Eur J Pharm Sci.
, vol.33
, Issue.2
, pp. 159-165
-
-
Woo, J.S.1
Song, Y.-K.2
Hong, J.-Y.3
Lim, S.-J.4
Kim, C.-K.5
-
307
-
-
23844542459
-
Effect of solubilizing and microemulsifying excipients in polyethylene glycol 6000 solid dispersion on enhanced dissolution and bioavailability of ketoconazole
-
Heo MY, Piao ZZ, Kim TW, Cao QR, Kim A, Lee BJ. Effect of solubilizing and microemulsifying excipients in polyethylene glycol 6000 solid dispersion on enhanced dissolution and bioavailability of ketoconazole. Arch Pharm Res. 2005;28(5):604-11
-
(2005)
Arch Pharm Res.
, vol.28
, Issue.5
, pp. 604-611
-
-
Heo, M.Y.1
Piao, Z.Z.2
Kim, T.W.3
Cao, Q.R.4
Kim, A.5
Lee, B.J.6
-
308
-
-
33644813455
-
Bioavailability assessment of ketoprofen incorporated in gelled self-emulsifying formulation: A technical note
-
Patil PR, Praveen S, Shobha Rani RH, Paradkar AR. Bioavailability assessment of ketoprofen incorporated in gelled self-emulsifying formulation: a technical note. AAPS PharmSciTech. 2005;6(1): E9-13
-
(2005)
AAPS PharmSciTech.
, vol.6
, Issue.1
-
-
Patil, P.R.1
Praveen, S.2
Shobha Rani, R.H.3
Paradkar, A.R.4
-
309
-
-
0029895433
-
Comparative bioavailability of L-683,453, a 5alpha-reductase inhibitor, from a self-emulsifying drug delivery system in beagle dogs
-
Matuszewska B, Hettrick L, Bondi JV, Storey DE. Comparative bioavailability of L-683,453, a 5alpha-reductase inhibitor, from a self-emulsifying drug delivery system in beagle dogs. Int J Pharm. 1996;136(1-2):147-54
-
(1996)
Int J Pharm.
, vol.136
, Issue.1-2
, pp. 147-154
-
-
Matuszewska, B.1
Hettrick, L.2
Bondi, J.V.3
Storey, D.E.4
-
310
-
-
76849084336
-
Preparation and evaluation of self-nanoemulsified drug delivery systems (SNEDDSs) of matrine based on drug-phospholipid complex technique
-
Dec 2. [Epub ahead of print]
-
Ruan J, Liu J, Zhu D, Gong T, Yang F, Hao X, Zhang Z. Preparation and evaluation of self-nanoemulsified drug delivery systems (SNEDDSs) of matrine based on drug-phospholipid complex technique. Int J Pharm. 2009 Dec 2. [Epub ahead of print]
-
(2009)
Int J Pharm.
-
-
Ruan, J.1
Liu, J.2
Zhu, D.3
Gong, T.4
Yang, F.5
Hao, X.6
Zhang, Z.7
-
311
-
-
76849097637
-
Development of microemulsion of mitotane for improvement of oral bioavailability
-
Sep 24. [Epub ahead of print]
-
Attivi D, Ajana I, Astier A, Demore B, Gibaud S. Development of microemulsion of mitotane for improvement of oral bioavailability. Drug Dev Ind Pharm. 2009 Sep 24. [Epub ahead of print]
-
(2009)
Drug Dev Ind Pharm.
-
-
Attivi, D.1
Ajana, I.2
Astier, A.3
Demore, B.4
Gibaud, S.5
-
312
-
-
70449532105
-
Solid self-emulsifying nitrendipine pellets: Preparation and in vitro/in vivo evaluation
-
Jan 4
-
Wang Z, Sun J, Wang Y, Liu X, Liu Y, Fu Q, Meng P, He Z. Solid self-emulsifying nitrendipine pellets: preparation and in vitro/in vivo evaluation. Int J Pharm. 2010 Jan 4;383(1-2):1-6
-
(2010)
Int J Pharm.
, vol.383
, Issue.1-2
, pp. 1-6
-
-
Wang, Z.1
Sun, J.2
Wang, Y.3
Liu, X.4
Liu, Y.5
Fu, Q.6
Meng, P.7
He, Z.8
-
313
-
-
67549123935
-
Formulation development and bioavailability evaluation of a self-nanoemulsified drug delivery system of oleanolic acid
-
Xi J, Chang Q, Chan CK, Meng ZY, Wang GN, Sun JB, Wang YT, Tong HH, Zheng Y. Formulation development and bioavailability evaluation of a self-nanoemulsified drug delivery system of oleanolic acid. AAPS PharmSciTech. 2009;10(1):172-82
-
(2009)
AAPS PharmSciTech.
, vol.10
, Issue.1
, pp. 172-182
-
-
Xi, J.1
Chang, Q.2
Chan, C.K.3
Meng, Z.Y.4
Wang, G.N.5
Sun, J.B.6
Wang, Y.T.7
Tong, H.H.8
Zheng, Y.9
-
314
-
-
33646227652
-
An alternative paclitaxel self-emulsifying microemulsion formulation: Preparation, pharmacokinetic profile, and hypersensitivity evaluation
-
Zhang XN, Tang LH, Gong JH, Yan XY, Zhang Q. An alternative paclitaxel self-emulsifying microemulsion formulation: preparation, pharmacokinetic profile, and hypersensitivity evaluation. PDA J Pharm Sci Technol. 2006;60(2):89-94
-
(2006)
PDA J Pharm Sci Technol.
, vol.60
, Issue.2
, pp. 89-94
-
-
Zhang, X.N.1
Tang, L.H.2
Gong, J.H.3
Yan, X.Y.4
Zhang, Q.5
-
315
-
-
53849089890
-
Formulation and in vitro and in vivo characterization of a phenytoin self-emulsifying drug delivery system (SEDDS)
-
Atef E, Belmonte AA. Formulation and in vitro and in vivo characterization of a phenytoin self-emulsifying drug delivery system (SEDDS). Eur J Pharm Sci. 2008;35(4):257-63
-
(2008)
Eur J Pharm Sci.
, vol.35
, Issue.4
, pp. 257-263
-
-
Atef, E.1
Belmonte, A.A.2
-
316
-
-
50249175117
-
Self-nanoemulsifying drug delivery system (SNEDDS) for oral delivery of protein drugs: III. in vivo oral absorption study
-
Rao SVR, Yajurvedi K, Shao J. Self-nanoemulsifying drug delivery system (SNEDDS) for oral delivery of protein drugs: III. In vivo oral absorption study. Int J Pharm. 2008;362(1-2):16-9
-
(2008)
Int J Pharm.
, vol.362
, Issue.1-2
, pp. 16-19
-
-
Rao, S.V.R.1
Yajurvedi, K.2
Shao, J.3
-
317
-
-
22244443039
-
Study on the bioavailability of puerarin from Pueraria lobata isoflavone self-microemulsifying drugdelivery systems and tablets in rabbits by liquid chromatography-mass spectrometry
-
Cui S, Zhao C, Tang X, Chen D, He Z. Study on the bioavailability of puerarin from Pueraria lobata isoflavone self-microemulsifying drugdelivery systems and tablets in rabbits by liquid chromatography-mass spectrometry. Biomed Chromatogr. 2005;19(5):375-8
-
(2005)
Biomed Chromatogr.
, vol.19
, Issue.5
, pp. 375-378
-
-
Cui, S.1
Zhao, C.2
Tang, X.3
Chen, D.4
He, Z.5
-
318
-
-
48949121068
-
Assessment of Pueraria lobata isoflavone with self-microemulsifying drug delivery systems in vitro and in vivo
-
Cui SM, Zhao CS, He ZG. Assessment of Pueraria lobata isoflavone with self-microemulsifying drug delivery systems in vitro and in vivo. Zhong Yao Cai. 2007;30(6):684-7
-
(2007)
Zhong Yao Cai.
, vol.30
, Issue.6
, pp. 684-687
-
-
Cui, S.M.1
Zhao, C.S.2
He, Z.G.3
-
319
-
-
0030769322
-
Phase I/II study of the toxicity, pharmacokinetics, and activity of the HIV protease inhibitor SC-52151
-
Fischl MA, Richman DD, Flexner C, Para MF, Haubrich R, Karim A, Yeramian P, Holden-Wiltse J, Meehan PM. Phase I/II study of the toxicity, pharmacokinetics, and activity of the HIV protease inhibitor SC-52151. J Acquir Immune Defic Syndr Hum Retrovirol. 1997;15(1):28-34
-
(1997)
J Acquir Immune Defic Syndr Hum Retrovirol.
, vol.15
, Issue.1
, pp. 28-34
-
-
Fischl, M.A.1
Richman, D.D.2
Flexner, C.3
Para, M.F.4
Haubrich, R.5
Karim, A.6
Yeramian, P.7
Holden-Wiltse, J.8
Meehan, P.M.9
-
320
-
-
33645214019
-
Disposition of lipidbased formulation in the intestinal tract affects the absorption of poorly water-soluble drugs
-
Iwanaga K, Kushibiki T, Miyazaki M, Kakemi M. Disposition of lipidbased formulation in the intestinal tract affects the absorption of poorly water-soluble drugs. Biol Pharm Bull. 2006;29(3):508-12
-
(2006)
Biol Pharm Bull.
, vol.29
, Issue.3
, pp. 508-512
-
-
Iwanaga, K.1
Kushibiki, T.2
Miyazaki, M.3
Kakemi, M.4
-
321
-
-
38749152100
-
Development of a selfemulsifying formulation that reduces the food effect for torcetrapib
-
Perlman ME, Murdande SB, Gumkowski MJ, Shah TS, Rodricks CM, Thornton-Manning J, Freel D, Erhart LC. Development of a selfemulsifying formulation that reduces the food effect for torcetrapib. Int J Pharm. 2008;351(1-2):15-22
-
(2008)
Int J Pharm.
, vol.351
, Issue.1-2
, pp. 15-22
-
-
Perlman, M.E.1
Murdande, S.B.2
Gumkowski, M.J.3
Shah, T.S.4
Rodricks, C.M.5
Thornton-Manning, J.6
Freel, D.7
Erhart, L.C.8
-
322
-
-
33644665457
-
Assesement of tretinoin with a self-emulsifying formulation in vitro and in vivo
-
Quan DQ, Xu GX. Assesement of tretinoin with a self-emulsifying formulation in vitro and in vivo. Yao Xue Xue Bao. 2005;40(1):76-9
-
(2005)
Yao Xue Xue Bao.
, vol.40
, Issue.1
, pp. 76-79
-
-
Quan, D.Q.1
Xu, G.X.2
-
323
-
-
68549115394
-
Comparison of self-microemulsifying drug delivery system versus solid dispersion technology used in the improvement of dissolution rate and bioavailability of vinpocetine
-
Chen Y, Li G, Huang JG, Wang RH, Liu H, Tang R. Comparison of self-microemulsifying drug delivery system versus solid dispersion technology used in the improvement of dissolution rate and bioavailability of vinpocetine. Yao Xue Xue Bao. 2009;44(6): 658-66
-
(2009)
Yao Xue Xue Bao.
, vol.44
, Issue.6
, pp. 658-666
-
-
Chen, Y.1
Li, G.2
Huang, J.G.3
Wang, R.H.4
Liu, H.5
Tang, R.6
-
324
-
-
67049143460
-
Preparation and evaluation of self-microemulsifying drug delivery system containing vinpocetine
-
Cui SX, Nie SF, Li L, Wang CG, Pan WS, Sun JP. Preparation and evaluation of self-microemulsifying drug delivery system containing vinpocetine. Drug Dev Ind Pharm. 2009;35(5):603-11
-
(2009)
Drug Dev Ind Pharm.
, vol.35
, Issue.5
, pp. 603-611
-
-
Cui, S.X.1
Nie, S.F.2
Li, L.3
Wang, C.G.4
Pan, W.S.5
Sun, J.P.6
-
325
-
-
34548094059
-
Bioavailability assessment of vitamin A self-nanoemulsified drug delivery systems in rats: A comparative study
-
Taha E, Ghorab D, Zaghloul AA. Bioavailability assessment of vitamin A self-nanoemulsified drug delivery systems in rats: a comparative study. Med Princ Pract. 2007;16(5):355-9.
-
(2007)
Med Princ Pract.
, vol.16
, Issue.5
, pp. 355-359
-
-
Taha, E.1
Ghorab, D.2
Zaghloul, A.A.3
-
326
-
-
70449524336
-
Selfnanoemulsifying drug delivery system (SNEDDS) for oral delivery of Zedoary essential oil: Formulation and bioavailability studies
-
Zhao Y, Wang C, Chow AH, Ren K, Gong T, Zhang Z, Zheng Y. Selfnanoemulsifying drug delivery system (SNEDDS) for oral delivery of Zedoary essential oil: formulation and bioavailability studies. Int J Pharm. 2010;383(1-2):170-7
-
(2010)
Int J Pharm.
, vol.383
, Issue.1-2
, pp. 170-177
-
-
Zhao, Y.1
Wang, C.2
Chow, A.H.3
Ren, K.4
Gong, T.5
Zhang, Z.6
Zheng, Y.7
-
327
-
-
33644626617
-
Study of the preparation of sustained-release microspheres containing zedoary turmeric oil by the emulsion-solvent-diffusion method and evaluation of the self-emulsification and bioavailability of the oil
-
You J, Cui FD, Han X, Wang YS, Yang L, Yu YW, Li QP. Study of the preparation of sustained-release microspheres containing zedoary turmeric oil by the emulsion-solvent-diffusion method and evaluation of the self-emulsification and bioavailability of the oil. Colloids Surf B Biointerfaces. 2006;48(1):35-41.
-
(2006)
Colloids Surf B Biointerfaces.
, vol.48
, Issue.1
, pp. 35-41
-
-
You, J.1
Cui, F.D.2
Han, X.3
Wang, Y.S.4
Yang, L.5
Yu, Y.W.6
Li, Q.P.7
-
328
-
-
70449524336
-
Selfnanoemulsifying drug delivery system (SNEDDS) for oral delivery of Zedoary essential oil: Formulation and bioavailability studies
-
Zhao Y, Wang C, Chow AH, Ren K, Gong T, Zhang Z, Zheng Y. Selfnanoemulsifying drug delivery system (SNEDDS) for oral delivery of Zedoary essential oil: Formulation and bioavailability studies. Int J Pharm. 2010;383(1-2):170-7.
-
(2010)
Int J Pharm.
, vol.383
, Issue.1-2
, pp. 170-177
-
-
Zhao, Y.1
Wang, C.2
Chow, A.H.3
Ren, K.4
Gong, T.5
Zhang, Z.6
Zheng, Y.7
-
329
-
-
0000483832
-
The portal transport of absorbed fatty acids
-
Kiyasu JY, Bloom B, Chaikoff IL. The portal transport of absorbed fatty acids. J Biol Chem. 1952;199(1):415-9
-
(1952)
J Biol Chem.
, vol.199
, Issue.1
, pp. 415-419
-
-
Kiyasu, J.Y.1
Bloom, B.2
Chaikoff, I.L.3
-
330
-
-
1942498896
-
Use of in vitro lipid digestion data to explain the in vivo performance of triglyceride-based oral lipid formulations of poorly water-soluble drugs: Studies with halofantrine
-
Porter CJ, Kaukonen AM, Taillardat-Bertschinger A, Boyd BJ, OConnor JM, Edwards GA, Charman WN. Use of in vitro lipid digestion data to explain the in vivo performance of triglyceride-based oral lipid formulations of poorly water-soluble drugs: studies with halofantrine. J Pharm Sci. 2004;93(5):1110-21
-
(2004)
J Pharm Sci.
, vol.93
, Issue.5
, pp. 1110-1121
-
-
Porter, C.J.1
Kaukonen, A.M.2
Taillardat-Bertschinger, A.3
Boyd, B.J.4
Oconnor, J.M.5
Edwards, G.A.6
Charman, W.N.7
-
331
-
-
0027946628
-
Intestinal permeability enhancement: Structure-activity and structure-toxicity relationships for nonylphenoxypolyoxyethylene surfactant permeability enhancers
-
Swenson ES, Milisen WB, Curatolo W. Intestinal permeability enhancement: structure-activity and structure-toxicity relationships for nonylphenoxypolyoxyethylene surfactant permeability enhancers. Pharm Res. 1994;11(10):1501-4
-
(1994)
Pharm Res.
, vol.11
, Issue.10
, pp. 1501-1504
-
-
Swenson, E.S.1
Milisen, W.B.2
Curatolo, W.3
-
333
-
-
37249007168
-
-
European Medicines Agency Available online at Accessed January 20
-
European Medicines Agency. EPARs for authorised medicinal products for human use. Available online at: http://www.emea.europa.eu/ humandocs/Humans/ EPAR/agenerase/agenerase.htm. Accessed January 20, 2010
-
(2010)
EPARs for Authorised Medicinal Products for Human Use
-
-
|