-
1
-
-
67449116319
-
Enhanced oral bioavailability of dexibuprofen by a novel solid self-emulsifying drug delivery system (SEDDS)
-
Balakrishnan P., Lee B.J., Oh D.H., Kim J.O., Hong M.J., Jee J.P., Kim J.A., Yoo B.K., Woo J.S., Yong C.S., Choi H.G. Enhanced oral bioavailability of dexibuprofen by a novel solid self-emulsifying drug delivery system (SEDDS). Eur. J. Pharm. Biopharm. 2009, 72:539-545.
-
(2009)
Eur. J. Pharm. Biopharm.
, vol.72
, 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
-
2
-
-
36248980358
-
The effects of pharmaceutical excipients on drug disposition
-
Buggins T.R., Dickinson P.A., Taylor G. The effects of pharmaceutical excipients on drug disposition. Adv. Drug Deliv. Rev. 2007, 59:1482-1503.
-
(2007)
Adv. Drug Deliv. Rev.
, vol.59
, pp. 1482-1503
-
-
Buggins, T.R.1
Dickinson, P.A.2
Taylor, G.3
-
3
-
-
39149124830
-
Lipid excipients and delivery systems for pharmaceutical development: a regulatory perspective
-
Chen M.L. Lipid excipients and delivery systems for pharmaceutical development: a regulatory perspective. Adv. Drug Deliv. Rev. 2008, 60:768-777.
-
(2008)
Adv. Drug Deliv. Rev.
, vol.60
, pp. 768-777
-
-
Chen, M.L.1
-
4
-
-
33845576641
-
Design and evaluation of self-nanoemulsifying drug delivery systems (SNEDDS) for cefpodoxime proxetil
-
Date A.A., Nagarsenker M.S. Design and evaluation of self-nanoemulsifying drug delivery systems (SNEDDS) for cefpodoxime proxetil. Int. J. Pharm. 2007, 329:166-172.
-
(2007)
Int. J. Pharm.
, vol.329
, pp. 166-172
-
-
Date, A.A.1
Nagarsenker, M.S.2
-
5
-
-
0036468854
-
Photodegradation studies on lacidipine in solution: basic experiments with a cis-trans reversible photoequilibrium under UV-A radiation exposure
-
De Filippis P., Bovina E., Da Ros L., Fiori J., Cavrini V. Photodegradation studies on lacidipine in solution: basic experiments with a cis-trans reversible photoequilibrium under UV-A radiation exposure. J. Pharm. Biomed. Anal. 2002, 27:803-812.
-
(2002)
J. Pharm. Biomed. Anal.
, vol.27
, pp. 803-812
-
-
De Filippis, P.1
Bovina, E.2
Da Ros, L.3
Fiori, J.4
Cavrini, V.5
-
6
-
-
69749105594
-
Self-nanoemulsifying drug delivery systems of tamoxifen citrate: design and optimization
-
Elnaggar Y.S., El-Massik M.A., Abdallah O.Y. Self-nanoemulsifying drug delivery systems of tamoxifen citrate: design and optimization. Int. J. Pharm. 2009, 380:133-141.
-
(2009)
Int. J. Pharm.
, vol.380
, pp. 133-141
-
-
Elnaggar, Y.S.1
El-Massik, M.A.2
Abdallah, O.Y.3
-
7
-
-
4444273107
-
Application of a mixture experimental design in the optimization of a self-emulsifying formulation with a high drug load
-
Gao P., Witt M.J., Haskell R.J., Zamora K.M., Shifflett J.R. Application of a mixture experimental design in the optimization of a self-emulsifying formulation with a high drug load. Pharm. Dev. Technol. 2004, 9:301-309.
-
(2004)
Pharm. Dev. Technol.
, vol.9
, pp. 301-309
-
-
Gao, P.1
Witt, M.J.2
Haskell, R.J.3
Zamora, K.M.4
Shifflett, J.R.5
-
8
-
-
33749454734
-
Optimization of self-microemulsifying drug delivery systems (SMEDDS) using a D-optimal design and the desirability function
-
Holm R., Jensen I.H., Sonnergaard J. Optimization of self-microemulsifying drug delivery systems (SMEDDS) using a D-optimal design and the desirability function. Drug Dev. Ind. Pharm. 2006, 32:1025-1032.
-
(2006)
Drug Dev. Ind. Pharm.
, vol.32
, pp. 1025-1032
-
-
Holm, R.1
Jensen, I.H.2
Sonnergaard, J.3
-
9
-
-
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, 110:332-338.
-
(2006)
J. Control Release
, vol.110
, pp. 332-338
-
-
Hong, J.Y.1
Kim, J.K.2
Song, Y.K.3
Park, J.S.4
Kim, C.K.5
-
10
-
-
11844284788
-
Optimization of pH-independent release of nicardipine hydrochloride extended-release matrix tablets using response surface methodology
-
Huang Y.B., Tsai Y.H., Lee S.H., Chang J.S., Wu P.C. Optimization of pH-independent release of nicardipine hydrochloride extended-release matrix tablets using response surface methodology. Int. J. Pharm. 2005, 289:87-95.
-
(2005)
Int. J. Pharm.
, vol.289
, pp. 87-95
-
-
Huang, Y.B.1
Tsai, Y.H.2
Lee, S.H.3
Chang, J.S.4
Wu, P.C.5
-
11
-
-
4644296179
-
Once-daily propranolol extended-release tablet dosage form: formulation design and in vitro/in vivo investigation
-
Huang Y.B., Tsai Y.H., Yang W.C., Chang J.S., Wu P.C., Takayama K. Once-daily propranolol extended-release tablet dosage form: formulation design and in vitro/in vivo investigation. Eur. J. Pharm. Biopharm. 2004, 58:607-614.
-
(2004)
Eur. J. Pharm. Biopharm.
, vol.58
, pp. 607-614
-
-
Huang, Y.B.1
Tsai, Y.H.2
Yang, W.C.3
Chang, J.S.4
Wu, P.C.5
Takayama, K.6
-
12
-
-
0036849503
-
In vitro and in situ evidence for the contribution of Labrasol and Gelucire 44/14 on transport of cephalexin and cefoperazone by rat intestine
-
Koga K., Kawashima S., Murakami M. In vitro and in situ evidence for the contribution of Labrasol and Gelucire 44/14 on transport of cephalexin and cefoperazone by rat intestine. Eur. J. Pharm. Biopharm. 2002, 54:311-318.
-
(2002)
Eur. J. Pharm. Biopharm.
, vol.54
, pp. 311-318
-
-
Koga, K.1
Kawashima, S.2
Murakami, M.3
-
13
-
-
0035895309
-
Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10: formulation development and bioavailability assessment
-
Kommuru T.R., Gurley B., Khan M.A., Reddy I.K. Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10: formulation development and bioavailability assessment. Int. J. Pharm. 2001, 212:233-246.
-
(2001)
Int. J. Pharm.
, vol.212
, pp. 233-246
-
-
Kommuru, T.R.1
Gurley, B.2
Khan, M.A.3
Reddy, I.K.4
-
14
-
-
0027997397
-
Lacidipine. A review of its pharmacodynamic and pharmacokinetic properties and therapeutic potential in the treatment of hypertension
-
Lee C.R., Bryson H.M. Lacidipine. A review of its pharmacodynamic and pharmacokinetic properties and therapeutic potential in the treatment of hypertension. Drugs 1994, 48:274-296.
-
(1994)
Drugs
, vol.48
, pp. 274-296
-
-
Lee, C.R.1
Bryson, H.M.2
-
15
-
-
10644257823
-
Effect of combined use of nonionic surfactant on formation of oil-in-water microemulsions
-
Lia P., Ghosha A., Wagnera R.F., Krillb S., Joshia Y.M., Serajuddin A.T.M. Effect of combined use of nonionic surfactant on formation of oil-in-water microemulsions. Int. J. Pharm. 2005, 288:27-34.
-
(2005)
Int. J. Pharm.
, vol.288
, pp. 27-34
-
-
Lia, P.1
Ghosha, A.2
Wagnera, R.F.3
Krillb, S.4
Joshia, Y.M.5
Serajuddin, A.T.M.6
-
16
-
-
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, 365:136-142.
-
(2009)
Int. J. Pharm.
, vol.365
, pp. 136-142
-
-
Liu, Y.1
Zhang, P.2
Feng, N.3
Zhang, X.4
Wu, S.5
Zhao, J.6
-
17
-
-
0142186090
-
Lacidipine: a review of its use in the management of hypertension
-
McCormack P.L., Wagstaff A.J. Lacidipine: a review of its use in the management of hypertension. Drugs 2003, 63:2327-2356.
-
(2003)
Drugs
, vol.63
, pp. 2327-2356
-
-
McCormack, P.L.1
Wagstaff, A.J.2
-
18
-
-
40149108427
-
Hydrogel-thickened nanoemulsion system for topical delivery of lipophilic drugs
-
Mou D., Chen H., Du D., Mao C., Wan J., Xu H., Yang X. Hydrogel-thickened nanoemulsion system for topical delivery of lipophilic drugs. Int. J. Pharm. 2008, 353:270-276.
-
(2008)
Int. J. Pharm.
, vol.353
, pp. 270-276
-
-
Mou, D.1
Chen, H.2
Du, D.3
Mao, C.4
Wan, J.5
Xu, H.6
Yang, X.7
-
19
-
-
0035940057
-
Intestinal lymphatic drug transport: an update
-
Porter C.J., Charman W.N. Intestinal lymphatic drug transport: an update. Adv. Drug Deliv. Rev. 2001, 50:61-80.
-
(2001)
Adv. Drug Deliv. Rev.
, vol.50
, pp. 61-80
-
-
Porter, C.J.1
Charman, W.N.2
-
20
-
-
39149092022
-
Enhancing intestinal drug solubilisation using lipid-based delivery systems
-
Porter C.J., Pouton C.W., Cuine J.F., Charman W.N. Enhancing intestinal drug solubilisation using lipid-based delivery systems. Adv. Drug Deliv. Rev. 2008, 60:673-691.
-
(2008)
Adv. Drug Deliv. Rev.
, vol.60
, pp. 673-691
-
-
Porter, C.J.1
Pouton, C.W.2
Cuine, J.F.3
Charman, W.N.4
-
21
-
-
33751014029
-
Formulation of poorly water-soluble drugs for oral administration: physicochemical and physiological issues and the lipid formulation classification system
-
Pouton C.W. Formulation of poorly water-soluble drugs for oral administration: physicochemical and physiological issues and the lipid formulation classification system. Eur. J. Pharm. Sci. 2006, 29:278-287.
-
(2006)
Eur. J. Pharm. Sci.
, vol.29
, pp. 278-287
-
-
Pouton, C.W.1
-
22
-
-
79953783032
-
Properties and uses of common formulation lipids, surfactants and cosolvents
-
Pouton C.W. Properties and uses of common formulation lipids, surfactants and cosolvents. AAPS Workshop 2007, http://www.aapspharmaceutica.com/meetings/files/85/03poultona.pdf.
-
(2007)
AAPS Workshop
-
-
Pouton, C.W.1
-
23
-
-
0037413364
-
Enhanced intestinal absorption of vancomycin with Labrasol and d-alpha-tocopheryl PEG 1000 succinate in rats
-
Prasad Y.V., Puthli S.P., Eaimtrakarn S., Ishida M., Yoshikawa Y., Shibata N., Takada K. Enhanced intestinal absorption of vancomycin with Labrasol and d-alpha-tocopheryl PEG 1000 succinate in rats. Int. J. Pharm. 2003, 250:181-190.
-
(2003)
Int. J. Pharm.
, vol.250
, pp. 181-190
-
-
Prasad, Y.V.1
Puthli, S.P.2
Eaimtrakarn, S.3
Ishida, M.4
Yoshikawa, Y.5
Shibata, N.6
Takada, K.7
-
24
-
-
39149097505
-
What determines drug solubility in lipid vehicles: is it predictable?
-
Rane S.S., Anderson B.D. What determines drug solubility in lipid vehicles: is it predictable?. Adv. Drug Deliv. Rev. 2008, 60:638-656.
-
(2008)
Adv. Drug Deliv. Rev.
, vol.60
, pp. 638-656
-
-
Rane, S.S.1
Anderson, B.D.2
-
25
-
-
50249132541
-
Self-nanoemulsifying drug delivery systems (SNEDDS) for oral delivery of protein drugs: I. Formulation development
-
Rao S.V., Shao J. Self-nanoemulsifying drug delivery systems (SNEDDS) for oral delivery of protein drugs: I. Formulation development. Int. J. Pharm. 2008, 362:2-9.
-
(2008)
Int. J. Pharm.
, vol.362
, pp. 2-9
-
-
Rao, S.V.1
Shao, J.2
-
26
-
-
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, 58:1183-1191.
-
(2006)
J. Pharm. Pharmacol.
, vol.58
, pp. 1183-1191
-
-
Shen, H.1
Zhong, M.2
-
27
-
-
21644461482
-
Formulation design of self-microemulsifying drug delivery systems for improved oral bioavailability of celecoxib
-
Subramanian N., Ray S., Ghosal S.K., Bhadra R., Moulik S.P. Formulation design of self-microemulsifying drug delivery systems for improved oral bioavailability of celecoxib. Biol. Pharm. Bull. 2004, 27:1993-1999.
-
(2004)
Biol. Pharm. Bull.
, vol.27
, pp. 1993-1999
-
-
Subramanian, N.1
Ray, S.2
Ghosal, S.K.3
Bhadra, R.4
Moulik, S.P.5
-
28
-
-
5444247353
-
Preparation and in vitro characterization of self-nanoemulsified drug delivery system (SNEDDS) of all-trans-retinol acetate
-
Taha E.I., Al-Saidan S., Samy A.M., Khan M.A. Preparation and in vitro characterization of self-nanoemulsified drug delivery system (SNEDDS) of all-trans-retinol acetate. Int. J. Pharm. 2004, 285:109-119.
-
(2004)
Int. J. Pharm.
, vol.285
, pp. 109-119
-
-
Taha, E.I.1
Al-Saidan, S.2
Samy, A.M.3
Khan, M.A.4
-
29
-
-
44749087578
-
Ultra-performance liquid chromatography-tandem mass spectrometry for the determination of lacidipine in human plasma and its application in a pharmacokinetic study
-
Tang J., Zhu R., Zhao R., Cheng G., Peng W. Ultra-performance liquid chromatography-tandem mass spectrometry for the determination of lacidipine in human plasma and its application in a pharmacokinetic study. J. Pharm. Biomed. Anal. 2008, 47:923-928.
-
(2008)
J. Pharm. Biomed. Anal.
, vol.47
, pp. 923-928
-
-
Tang, J.1
Zhu, R.2
Zhao, R.3
Cheng, G.4
Peng, W.5
-
30
-
-
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, 383:1-6.
-
(2010)
Int. J. Pharm.
, vol.383
, 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
-
31
-
-
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 E.K., Bartlett K., Gershkovich P., Sivak O., Banno B., Wong Z., Gagnon J., Gates B., Leon C.G., Wasan K.M. 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, 372:76-84.
-
(2009)
Int. J. Pharm.
, vol.372
, 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
-
32
-
-
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, 31:785-794.
-
(2005)
Drug Dev. Ind. Pharm.
, vol.31
, pp. 785-794
-
-
Wei, L.1
Sun, P.2
Nie, S.3
Pan, W.4
-
33
-
-
0033427847
-
Vitamin E-TPGS increases absorption flux of an HIV protease inhibitor by enhancing its solubility and permeability
-
Yu L., Bridgers A., Polli J., Vickers A., Long S., Roy A., Winnike R., Coffin M. Vitamin E-TPGS increases absorption flux of an HIV protease inhibitor by enhancing its solubility and permeability. Pharm. Res. 1999, 16:1812-1817.
-
(1999)
Pharm. Res.
, vol.16
, pp. 1812-1817
-
-
Yu, L.1
Bridgers, A.2
Polli, J.3
Vickers, A.4
Long, S.5
Roy, A.6
Winnike, R.7
Coffin, M.8
-
34
-
-
2642566037
-
Commonly used surfactant, Tween 80, improves absorption of P-glycoprotein substrate, digoxin, in rats
-
Zhang H., Yao M., Morrison R.A., Chong S. Commonly used surfactant, Tween 80, improves absorption of P-glycoprotein substrate, digoxin, in rats. Arch. Pharm. Res. 2003, 26:768-772.
-
(2003)
Arch. Pharm. Res.
, vol.26
, pp. 768-772
-
-
Zhang, H.1
Yao, M.2
Morrison, R.A.3
Chong, S.4
-
35
-
-
41349096647
-
Preparation and evaluation of self-microemulsifying drug delivery system of oridonin
-
Zhang P., Liu Y., Feng N., Xu J. Preparation and evaluation of self-microemulsifying drug delivery system of oridonin. Int. J. Pharm. 2008, 355:269-276.
-
(2008)
Int. J. Pharm.
, vol.355
, pp. 269-276
-
-
Zhang, P.1
Liu, Y.2
Feng, N.3
Xu, J.4
|