-
1
-
-
0000965958
-
Transparent water-in-oil dispersions: The oleopathic hydro-micelle
-
Hoar TP, Schulman JH. Transparent water-in-oil dispersions: The oleopathic hydro-micelle. Nature 1943;152:102-3
-
(1943)
Nature
, vol.152
, pp. 102-103
-
-
Hoar, T.P.1
Schulman, J.H.2
-
2
-
-
0001009759
-
Mechanism of formation and structure of micro emulsions by electron microscopy
-
Schulman J, Stoeckenius W. Mechanism of formation and structure of micro emulsions by electron microscopy. J Phys Chem 1959;63:1677-80
-
(1959)
J. Phys. Chem.
, vol.63
, pp. 1677-1680
-
-
Schulman, J.1
Stoeckenius, W.2
-
4
-
-
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
, Issue.130
, pp. 47-64
-
-
Spernath, A.1
Aserin, A.2
-
5
-
-
34548763353
-
Design and development of oral oil in water ramipril nanoemulsion formulation: In vitro and in vivo assessment
-
Shafiq S, Shakeel F, Talegaonkar S, et al. Design and development of oral oil in water ramipril nanoemulsion formulation: In vitro and in vivo assessment. J Biomed Nanotechnol 2007;3:28-44
-
(2007)
J. Biomed. Nanotechnol.
, vol.3
, pp. 28-44
-
-
Shafiq, S.1
Shakeel, F.2
Talegaonkar, S.3
-
6
-
-
78049499869
-
New perspectives on lipid and surfactant based drug delivery systems for oral delivery of poorly soluble drugs
-
Muellertz A, Ogbonna A, Ren S, et al. New perspectives on lipid and surfactant based drug delivery systems for oral delivery of poorly soluble drugs. J Pharm Pharmacol 2010;62:1622-36
-
(2010)
J. Pharm. Pharmacol.
, vol.62
, pp. 1622-1636
-
-
Muellertz, A.1
Ogbonna, A.2
Ren, S.3
-
7
-
-
52649101885
-
Physicochemical properties, pharmacokinetics, and pharmacodynamics of a reformulated microemulsion propofol in rats
-
Noh GJ, Lee E-H, Lee SH, et al. Physicochemical properties, pharmacokinetics, and pharmacodynamics of a reformulated microemulsion propofol in rats. Anesthesiology 2008;109:436-47
-
(2008)
Anesthesiology
, vol.109
, pp. 436-447
-
-
Noh, G.J.1
Lee, E.-H.2
Lee, S.H.3
-
8
-
-
0037026275
-
Lecithin microemulsions for the topical administration of ketoprofen: Percutaneous adsorption through human skin and in vivo human skin tolerability
-
Paolino D, Ventura C, Nistico S, et al. Lecithin microemulsions for the topical administration of ketoprofen: Percutaneous adsorption through human skin and in vivo human skin tolerability. Int J Pharm 2002;244:21-31
-
(2002)
Int. J. Pharm.
, vol.244
, pp. 21-31
-
-
Paolino, D.1
Ventura, C.2
Nistico, S.3
-
9
-
-
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;329:166-72
-
(2007)
Int. J. Pharm.
, vol.329
, pp. 166-172
-
-
Date, A.A.1
Nagarsenker, M.S.2
-
10
-
-
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;29:278-87
-
(2006)
Eur. J. Pharm. Sci.
, vol.29
, pp. 278-287
-
-
Pouton, C.W.1
-
11
-
-
0033805858
-
Lipid formulations for oral administration of drugs: Non-emulsifying, self-emulsifying and 'self-microemulsifying' drug delivery systems
-
Pouton CW. Lipid formulations for oral administration of drugs: Non-emulsifying, 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. 12
-
-
Pouton, C.W.1
-
12
-
-
0034880214
-
Cremophor EL: The drawbacks and advantages of vehicle selection for drug formulation
-
Gelderblom H, Verweij J, Nooter K, et al. Cremophor EL: The drawbacks and advantages of vehicle selection for drug formulation. Eur J Cancer 2001;37:1590-8
-
(2001)
Eur. J. Cancer
, vol.37
, pp. 1590-1598
-
-
Gelderblom, H.1
Verweij, J.2
Nooter, K.3
-
13
-
-
0015349672
-
Potentiation of drug effect by Tween 80 in Chinese hamster cells resistant to actinomycin D and daunomycin
-
Riehm H, Biedler JL. Potentiation of drug effect by Tween 80 in Chinese hamster cells resistant to actinomycin D and daunomycin. Cancer Res 1972;32:1195-200
-
(1972)
Cancer Res.
, vol.32
, pp. 1195-1200
-
-
Riehm, H.1
Biedler, J.L.2
-
14
-
-
0026101562
-
Solutol HS 15, nontoxic polyoxyethylene esters of 12-hydroxystearic acid, reverses multidrug resistance
-
Coon JS, Knudson W, Clodfelter K, et al. Solutol HS 15, nontoxic polyoxyethylene esters of 12-hydroxystearic acid, reverses multidrug resistance. Cancer Res 1991;51:897-902
-
(1991)
Cancer Res.
, vol.51
, pp. 897-902
-
-
Coon, J.S.1
Knudson, W.2
Clodfelter, K.3
-
15
-
-
0027136158
-
Effects of nonionic detergents on P-glycoprotein drug binding and reversal of multidrug resistance
-
Zordan-Nudo T, Ling V, Liu Z, et al. Effects of nonionic detergents on P-glycoprotein drug binding and reversal of multidrug resistance. Cancer Res 1993;53:5994-6000
-
(1993)
Cancer Res.
, vol.53
, pp. 5994-6000
-
-
Zordan-Nudo, T.1
Ling, V.2
Liu, Z.3
-
16
-
-
0026586447
-
Self-emulsifying drug delivery systems: Formulation and biopharmaceutic evaluation of an investigational lipophilic compound
-
Charman SA, Charman WN, Rogge MC, et al. Self-emulsifying drug delivery systems: Formulation and biopharmaceutic evaluation of an investigational lipophilic compound. Pharm Res 1992;9:87-93
-
(1992)
Pharm. Res.
, vol.9
, pp. 87-93
-
-
Charman, S.A.1
Charman, W.N.2
Rogge, M.C.3
-
17
-
-
0028194817
-
Self-emulsifying drug-delivery systems (SEDDS) with polyglycolyzed glycerides for improving in-vitro dissolution and oral absorption of lipophilic drugs
-
Shah N, Carvajal M, Patel C, et al. Self-emulsifying drug-delivery systems (SEDDS) with polyglycolyzed glycerides for improving in-vitro dissolution and oral absorption of lipophilic drugs. Int J Pharm 1994;106:15-23
-
(1994)
Int. J. Pharm.
, vol.106
, pp. 15-23
-
-
Shah, N.1
Carvajal, M.2
Patel, C.3
-
18
-
-
0343051915
-
Uptake of drugs into the intestinal lymphatics after oral administration
-
Porter CJH, Charman WN. Uptake of drugs into the intestinal lymphatics after oral administration. Adv Drug Deliv Rev 1997;25:71-89
-
(1997)
Adv. Drug Deliv. Rev.
, vol.25
, pp. 71-89
-
-
Porter, C.J.H.1
Charman, W.N.2
-
19
-
-
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 J, et al. 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;28:233-42
-
(2006)
Eur. J. Pharm. Sci.
, vol.28
, pp. 233-242
-
-
Grove, M.1
Mullertz, A.2
Nielsen, J.3
-
20
-
-
0005189510
-
Formation of microemulsions by aminoalkyl alcohols
-
Schulman JH, Montagne JB. Formation of microemulsions by aminoalkyl alcohols. Ann N Y Acad Sci 1961;92:366-71
-
(1961)
Ann. NY. Acad. Sci.
, vol.92
, pp. 366-371
-
-
Schulman, J.H.1
Montagne, J.B.2
-
21
-
-
0029050215
-
Investigations into the formation and characterization of phospholipid microemulsions. IV. Pseudo-ternary phase-diagrams of systems containing water-lecithin-alcohol and oil - The influence of oil
-
Aboofazeli R, Patel N, Thomas M, et al. Investigations into the formation and characterization of phospholipid microemulsions. IV. Pseudo-ternary phase-diagrams of systems containing water-lecithin-alcohol and oil-the influence of oil. Int J Pharm 1995;125:107-16
-
(1995)
Int. J. Pharm.
, vol.125
, pp. 107-116
-
-
Aboofazeli, R.1
Patel, N.2
Thomas, M.3
-
22
-
-
77749268044
-
Development of microemulsion of mitotane for improvement of oral bioavailability
-
Attivi D, Ajana I, Astier A, et al. Development of microemulsion of mitotane for improvement of oral bioavailability. Drug Dev Ind Pharm 2010;36:421-7
-
(2010)
Drug Dev. Ind. Pharm.
, vol.36
, pp. 421-427
-
-
Attivi, D.1
Ajana, I.2
Astier, A.3
-
23
-
-
34247609989
-
Development and bioavailability assessment of ramipril nanoemulsion formulation
-
Shafiq S, Shakeel F, Talegaonkar S, et al. Development and bioavailability assessment of ramipril nanoemulsion formulation. Eur J Pharm Biopharm 2007;66:227-43
-
(2007)
Eur. J. Pharm. Biopharm.
, vol.66
, pp. 227-243
-
-
Shafiq, S.1
Shakeel, F.2
Talegaonkar, S.3
-
24
-
-
1842609789
-
Development of self-microemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogs
-
Kang B, Lee J, Chon S, et al. Development of self-microemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogs. Int J Pharm 2004;274:65-73
-
(2004)
Int. J. Pharm.
, vol.274
, pp. 65-73
-
-
Kang, B.1
Lee, J.2
Chon, S.3
-
25
-
-
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, et al. 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;69:899-907
-
(2008)
Eur. J. Pharm. Biopharm.
, vol.69
, pp. 899-907
-
-
Lu, J.-L.1
Wang, J.-C.2
Zhao, S.-X.3
-
27
-
-
0037413394
-
An alternative paclitaxel microemulsion formulation: Hypersensitivity evaluation and pharmacokinetic profile
-
He L, Wang G-L, Zhang Q. An alternative paclitaxel microemulsion formulation: Hypersensitivity evaluation and pharmacokinetic profile. Int J Pharm 2003;250:45-50
-
(2003)
Int. J. Pharm.
, vol.250
, pp. 45-50
-
-
He, L.1
Wang, G.-L.2
Zhang, Q.3
-
28
-
-
33847665647
-
Formulation of a self-Emulsifying system for oral delivery of simvastatin: In vitro and in vivo evaluation
-
Patil P, Patil V, Paradkar A. Formulation of a self-emulsifying system for oral delivery of simvastatin: In vitro and in vivo evaluation. Acta Pharm 2007;57:111-22
-
(2007)
Acta. Pharm.
, vol.57
, pp. 111-122
-
-
Patil, P.1
Patil, V.2
Paradkar, A.3
-
29
-
-
0000049502
-
A theory of aqueous emulsions i negative interfacial tension at the oil/water interface
-
Prince LM. A theory of aqueous emulsions. I. Negative interfacial tension at the oil/water interface. J Colloid Interface Sci 1967;23:165-73
-
(1967)
J. Colloid Interface Sci.
, Issue.23
, pp. 165-173
-
-
Prince, L.M.1
-
30
-
-
84864217742
-
Static and dynamic interfacial tension analysis
-
Wrolstad RE Decker EA Schwartz SJ et al. editors Wiley-Interscience Hoboken, New Jersey
-
Weiss J. Static and dynamic interfacial tension analysis. In: Wrolstad RE, Decker EA, Schwartz SJ, et al. editors. Handbook of food analytical chemistry, water, proteins, enzymes, lipids, and carbohydrates. Wiley-Interscience; Hoboken, New Jersey: 2005. p. 631-46
-
(2005)
Handbook of Food Analytical Chemistry Water Proteins Enzymes Lipids and Carbohydrates
, pp. 631-46
-
-
Weiss, J.1
-
31
-
-
84867723296
-
Effect of cosurfactant on microemulsion phase behavior in NP7 surfactant system
-
Lim H, Lee S, Mo D, et al. Effect of cosurfactant on microemulsion phase behavior in NP7 surfactant system. J Korean Ind Eng Chem 2011;22:416-22
-
(2011)
J. Korean Ind. Eng. Chem.
, vol.22
, pp. 416-422
-
-
Lim, H.1
Lee, S.2
Mo, D.3
-
32
-
-
0242652719
-
Thermodynamic, interfacial, and structural properties of polyphasic microemulsion systems
-
Bellocq AM, Bourbon D, Lemanceau B, et al. Thermodynamic, interfacial, and structural properties of polyphasic microemulsion systems. J Colloid Interface Sci 1982;89:427-40
-
(1982)
J. Colloid Interface Sci.
, vol.89
, pp. 427-440
-
-
Bellocq, A.M.1
Bourbon, D.2
Lemanceau, B.3
-
33
-
-
79953645128
-
Screening the prescription microemulsion by conductivity and the phase behavior
-
Chen LH, Zhao XT, Wu DZ, et al. Screening the prescription microemulsion by conductivity and the phase behavior. Chin Pharm J 2011;46:40-3
-
(2011)
Chin. Pharm. J.
, vol.46
, pp. 40-43
-
-
Chen, L.H.1
Zhao, X.T.2
Wu, D.Z.3
-
34
-
-
0037925140
-
Comparative pharmacokinetics and safety of a novel lyophilized amphotericin B lecithin-based oil-water microemulsion and amphotericin B deoxycholate in animal models
-
Brime B, Frutos P, Bringas P, et al. Comparative pharmacokinetics and safety of a novel lyophilized amphotericin B lecithin-based oil-water microemulsion and amphotericin B deoxycholate in animal models. J Antimicrob Chemother 2003;52:103-9
-
(2003)
J. Antimicrob. Chemother.
, vol.52
, pp. 103-109
-
-
Brime, B.1
Frutos, P.2
Bringas, P.3
-
35
-
-
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;15:863-9
-
(1998)
Pharm. Res.
, vol.15
, pp. 863-869
-
-
Gershanik, T.1
Benzeno, S.2
Benita, S.3
-
36
-
-
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 R, Lambert G, et al. 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;21:261-70
-
(2004)
Pharm. Res.
, vol.21
, pp. 261-270
-
-
Yang, S.1
Gursoy, R.2
Lambert, G.3
-
37
-
-
79955924784
-
Microemulsion drug delivery system: Design and development for oral bioavailability enhancement of lovastatin
-
Mandal S. Microemulsion drug delivery system: Design and development for oral bioavailability enhancement of lovastatin. S Afr Pharm J 2011;78:44-50
-
(2011)
S. Afr. Pharm J.
, vol.78
, pp. 44-50
-
-
Mandal, S.1
-
38
-
-
78651250937
-
Development of microemulsion for solubility enhancement of clopidogrel
-
Patel V, Kukadiya H, Mashru R, et al. Development of microemulsion for solubility enhancement of clopidogrel. Iran J Pharm Res 2010;9:327-34
-
(2010)
Iran J. Pharm. Res.
, vol.9
, pp. 327-334
-
-
Patel, V.1
Kukadiya, H.2
Mashru, R.3
-
39
-
-
0001038403
-
Techniques for measuring the composition (Oil and Water-Content) of emulsions - A State-of-the-art review
-
Pal R. Techniques for measuring the composition (Oil and Water-Content) of emulsions - a State-of-the-art review. Colloid Surf A 1994;84:141-93
-
(1994)
Colloid Surf A
, vol.84
, pp. 141-193
-
-
Pal, R.1
-
40
-
-
33645986146
-
The novel formulation design of self-emulsifying 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 self-emulsifying 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;21:45-53
-
(2006)
Drug Metab. Pharmacokinet
, vol.21
, pp. 45-53
-
-
Araya, H.1
Tomita, M.2
Hayashi, M.3
-
41
-
-
0014154126
-
Reversible alterations of the surface of ascites tumour cells induced by a surface-active substance, Tween 60
-
Malenkov AG, Bogatyreva SA, Bozhkova VP, et al. Reversible alterations of the surface of ascites tumour cells induced by a surface-active substance, Tween 60. Exp Cell Res 1967;48:307-18
-
(1967)
Exp Cell Res.
, vol.48
, pp. 307-318
-
-
Malenkov, A.G.1
Bogatyreva, S.A.2
Bozhkova, V.P.3
-
42
-
-
70350618790
-
Docetaxel microemulsion for enhanced oral bioavailability: Preparation and in vitro and in vivo evaluation
-
Yin Y-M, Cui F-D, Mu C-F, et al. Docetaxel microemulsion for enhanced oral bioavailability: Preparation and in vitro and in vivo evaluation. J Control Release 2009;140:86-94
-
(2009)
J. Control Release
, vol.140
, pp. 86-94
-
-
Yin, Y.-M.1
Cui, F.-D.2
Mu, C.-F.3
-
44
-
-
74749094618
-
Thermal reversible microemulsion system for poorly water-soluble YH439 for oral delivery
-
Han D-H, Jin Z-H, Jin Y-Z, et al. Thermal reversible microemulsion system for poorly water-soluble YH439 for oral delivery. Chem Pharm Bull 2010;58:11-15
-
(2010)
Chem. Pharm. Bull.
, vol.58
, pp. 11-15
-
-
Han, D.-H.1
Jin, Z.-H.2
Jin, Y.-Z.3
-
45
-
-
39049164624
-
Microemulsions as novel drug carriers: The formation, stability, applications and toxicity
-
Karasulu H. Microemulsions as novel drug carriers: The formation, stability, applications and toxicity. Exp Opin Drug Deliv 2008;5:119-35
-
(2008)
Exp. Opin. Drug Deliv.
, vol.5
, pp. 119-135
-
-
Karasulu, H.1
-
46
-
-
15244353232
-
Effect of self-microemulsifying drug delivery systems containing Labrasol on tight junctions in Caco-2 cells
-
Sha X, Yan G, Wu Y, et al. Effect of self-microemulsifying drug delivery systems containing Labrasol on tight junctions in Caco-2 cells. Eur J Pharm Sci 2005;24:477-86
-
(2005)
Eur. J. Pharm. Sci.
, vol.24
, pp. 477-486
-
-
Sha, X.1
Yan, G.2
Wu, Y.3
-
47
-
-
41349109102
-
Parallel artificial membrane permeability assay (PAMPA) combined with a 10-day multiscreen Caco-2 cell culture as a tool for assessing new drug candidates
-
Masungi C, Mensch J, Van Dijck A, et al. Parallel artificial membrane permeability assay (PAMPA) combined with a 10-day multiscreen Caco-2 cell culture as a tool for assessing new drug candidates. Pharmazie 2008;63:194-9
-
(2008)
Pharmazie
, vol.63
, pp. 194-199
-
-
Masungi, C.1
Mensch, J.2
Van Dijck, A.3
-
48
-
-
0032568397
-
Physicochemical high throughput screening: Parallel artificial membrane permeation assay in the description of passive absorption processes
-
Kansy M, Senner F, Gubernator K. Physicochemical high throughput screening: Parallel artificial membrane permeation assay in the description of passive absorption processes. J Med Chem 1998; 41:1007-10
-
(1998)
J. Med. Chem.
, vol.41
, pp. 1007-1010
-
-
Kansy, M.1
Senner, F.2
Gubernator, K.3
-
49
-
-
44749090398
-
A novel design of artificial membrane for improving the PAMPA model
-
Chen X, Murawski A, Patel K, et al. A novel design of artificial membrane for improving the PAMPA model. Pharm Res 2008;25:1511-20
-
(2008)
Pharm. Res.
, vol.25
, pp. 1511-1520
-
-
Chen, X.1
Murawski, A.2
Patel, K.3
-
50
-
-
0024976004
-
Cyclosporine
-
Kahan BD. Cyclosporine. N Engl J Med 1989;321:1725-1738
-
(1989)
N. Engl. J. Med.
, vol.321
, pp. 1725-38
-
-
Kahan, B.D.1
-
51
-
-
0019502920
-
Cyclosporin A: Pharmacokinetics after a single dose in man and serum levels after multiple dosing in recipients of allogeneic bone-marrow grafts
-
Beveridge T, Gratwohl A, Michot F, et al. Cyclosporin A: Pharmacokinetics after a single dose in man and serum levels after multiple dosing in recipients of allogeneic bone-marrow grafts. Curr Ther Res 1981;30:5-18
-
(1981)
Curr. Ther. Res.
, vol.30
, pp. 5-18
-
-
Beveridge, T.1
Gratwohl, A.2
Michot, F.3
-
52
-
-
0023946993
-
Trough levels and concentration time curves of cyclosporine in patients undergoing renal transplantation
-
Frey FJ, Horber FF, Frey BM. Trough levels and concentration time curves of cyclosporine in patients undergoing renal transplantation. Clin Pharmacol Ther 1988;43:55-62
-
(1988)
Clin. Pharmacol. Ther.
, vol.43
, pp. 55-62
-
-
Frey, F.J.1
Horber, F.F.2
Frey, B.M.3
-
55
-
-
0022156731
-
Pharmacokinetics and monitoring of cyclosporine following orthotopic liver transplantation
-
Venkataramanan R, Burckhart GJ, Ptachcinski RJ. Pharmacokinetics and monitoring of cyclosporine following orthotopic liver transplantation. Semin Liver Dis 1985;5:357-68
-
(1985)
Semin. Liver Dis.
, vol.5
, pp. 357-368
-
-
Venkataramanan, R.1
Burckhart, G.J.2
Ptachcinski, R.J.3
-
56
-
-
0028998542
-
Absorption of cyclosporin from conventional and new microemulsion oral formulations in liver transplant recipients with external biliary diversion
-
Trull AK, Tan KKC, Tan L, et al. Absorption of cyclosporin from conventional and new microemulsion oral formulations in liver transplant recipients with external biliary diversion. Br J Clin Pharmacol 1995;39:627-31
-
(1995)
Br. J. Clin. Pharmacol.
, vol.39
, pp. 627-631
-
-
Trull, A.K.1
Tan, K.K.C.2
Tan, L.3
-
57
-
-
0028335905
-
Reduced inter- and intraindividual variability in cyclosporine pharmacokinetics from a microemulsion formulation
-
Kovarik JM, Mueller EA, Van Bree JB, et al. Reduced inter- and intraindividual variability in cyclosporine pharmacokinetics from a microemulsion formulation. J Pharm Sci 1994;83:444-6
-
(1994)
J. Pharm. Sci.
, vol.83
, pp. 444-446
-
-
Kovarik, J.M.1
Mueller, E.A.2
Van Bree, J.B.3
-
58
-
-
0027534967
-
Cyclosporin absorption from microemulsion formulation in liver transplant recipient
-
Trull AK, Tan KK, Uttridge J, et al. Cyclosporin absorption from microemulsion formulation in liver transplant recipient. Lancet 1993;341:433
-
(1993)
Lancet
, vol.341
, pp. 433
-
-
Trull, A.K.1
Tan, K.K.2
Uttridge, J.3
-
59
-
-
0022918334
-
Pharmacokinetics of oral cyclosporin a (Sandimmun) in healthy subjects
-
Grevel J, Nesch E, Abisch E, et al. Pharmacokinetics of oral cyclosporin a (Sandimmun) in healthy subjects. Eur J Clin Pharmacol 1986;31:211-16
-
(1986)
Eur. J. Clin. Pharmacol.
, vol.31
, pp. 211-216
-
-
Grevel, J.1
Nesch, E.2
Abisch, E.3
-
61
-
-
0028304606
-
Within-day consistency in cyclosporine pharmacokinetics from a microemulsion formulation in renal transplant patients
-
Kovarik JM, Mueller EA, Van Bree JB, et al. Within-day consistency in cyclosporine pharmacokinetics from a microemulsion formulation in renal transplant patients. Ther Drug Monit 1994;16:232-7
-
(1994)
Ther. Drug Monit.
, vol.16
, pp. 232-237
-
-
Kovarik, J.M.1
Mueller, E.A.2
Van Bree, J.B.3
-
62
-
-
0028329964
-
Improved dose linearity of cyclosporine pharmacokinetics from a microemulsion formulation
-
Mueller EA, Kovarik JM, Van Bree JB, et al. Improved dose linearity of cyclosporine pharmacokinetics from a microemulsion formulation. Pharm Res 1994;11:301-4
-
(1994)
Pharm. Res.
, vol.11
, pp. 301-304
-
-
Mueller, E.A.1
Kovarik, J.M.2
Van Bree, J.B.3
-
63
-
-
33745656817
-
A comparison of intestinal lymphatic transport and systemic bioavailability of saquinavir from three lipid-based formulations in the anaesthetised rat model
-
Griffin BT, O'Driscoll CM. A comparison of intestinal lymphatic transport and systemic bioavailability of saquinavir from three lipid-based formulations in the anaesthetised rat model. J Pharm Pharmacol 2006;58:917-25
-
(2006)
J. Pharm. Pharmacol.
, vol.58
, pp. 917-925
-
-
Griffin, B.T.1
O'Driscoll, C.M.2
-
64
-
-
0032504917
-
Effects of vitamin E and C supplementation on oxidative stress and viral load in HIV-infected subjects
-
Allard JP, Aghdassi E, Chau J, et al. Effects of vitamin E and C supplementation on oxidative stress and viral load in HIV-infected subjects. Aids 1998;12:1653
-
(1998)
Aids
, vol.12
, pp. 1653
-
-
Allard, J.P.1
Aghdassi, E.2
Chau, J.3
-
65
-
-
77953419716
-
Design and development of Saquinavir microemulsion for the oral bioavailability enhancement
-
Surjyanarayan M, Snigdha S M, Naazneen S, et al. Design and development of Saquinavir microemulsion for the oral bioavailability enhancement. Int J Pharm Tech Res 2009;1:1442-8
-
(2009)
Int. J. Pharm. Tech Res
, vol.1
, pp. 1442-1448
-
-
Surjyanarayan, M.1
Snigdha S, M.2
Naazneen, S.3
-
66
-
-
0035990403
-
Saquinavir soft-gel capsules (Fortovase) give lower exposure than expected, even after a high-Fat breakfast
-
Hugen PWH, Burger DM, Koopmans PP, et al. Saquinavir soft-gel capsules (Fortovase) give lower exposure than expected, even after a high-fat breakfast. Pharm World Sci 2002;24:83-6
-
(2002)
Pharm World Sci.
, vol.24
, pp. 83-86
-
-
Hugen, P.W.H.1
Burger, D.M.2
Koopmans, P.P.3
-
67
-
-
34848863347
-
Clinical studies with oral lipid based formulations of poorly soluble compounds
-
Fatouros DG, Karpf DM, Nielsen FS, et al. Clinical studies with oral lipid based formulations of poorly soluble compounds. Ther Clin Risk Manage 2007;3:591-604
-
(2007)
Ther. Clin. Risk Manage
, vol.3
, pp. 591-604
-
-
Fatouros, D.G.1
Karpf, D.M.2
Nielsen, F.S.3
-
68
-
-
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;66:173-81
-
(2007)
Eur. J. Pharm. Biopharm.
, vol.66
, pp. 173-181
-
-
Goddeeris, C.1
Coacci, J.2
Van Den Mooter, G.3
-
69
-
-
33749057113
-
Design and development of microemulsion drug delivery system of acyclovir for improvement of oral bioavailability
-
Ghosh PK, Majithiya RJ, Umrethia ML, et al. Design and development of microemulsion drug delivery system of acyclovir for improvement of oral bioavailability. AAPS PharmSciTech 2006;7:E1-6
-
(2006)
AAPS Pharm. Sci. Tech.
, vol.7
-
-
Ghosh, P.K.1
Majithiya, R.J.2
Umrethia, M.L.3
-
70
-
-
79960796807
-
Preparation and evaluation of the self emulsifying drug delivery system containing atorvastatin HMG-CoA inhibiter
-
Chouksey R, Pandey H, Jain AK, et al. Preparation and evaluation of the self emulsifying drug delivery system containing atorvastatin HMG-CoA inhibiter. Int J Pharm Pharm Sci 2011;3:147-52
-
(2011)
Int. J. Pharm. Pharm Sci
, vol.3
, pp. 147-152
-
-
Chouksey, R.1
Pandey, H.2
Jain, A.K.3
-
71
-
-
70349840419
-
Combined hydroxypropyl-beta-cyclodextrin and poly(anhydride) nanoparticles improve the oral permeability of paclitaxel
-
Agueros M, Ruiz-Gaton L, Vauthier C, et al. Combined hydroxypropyl-beta- cyclodextrin and poly(anhydride) nanoparticles improve the oral permeability of paclitaxel. Eur J Pharm Sci 2009;38:405-13
-
(2009)
Eur. J. Pharm. Sci.
, vol.38
, pp. 405-413
-
-
Agueros, M.1
Ruiz-Gaton, L.2
Vauthier, C.3
-
72
-
-
0028838372
-
Pharmaceutical and physical properties of paclitaxel (Taxol) complexes with cyclodextrins
-
Sharma U, Balasubramanian S, Straubinger R. Pharmaceutical and physical properties of paclitaxel (Taxol) complexes with cyclodextrins. J Pharm Sci 1995;84:1223-30
-
(1995)
J. Pharm. Sci.
, vol.84
, pp. 1223-1230
-
-
Sharma, U.1
Balasubramanian, S.2
Straubinger, R.3
-
73
-
-
34447545904
-
Novel enhanced delivery taxanes: An update
-
Perez EA. Novel enhanced delivery taxanes: An update. Semin Oncol 2007;34:S1-5
-
(2007)
Semin. Oncol.
, vol.34
-
-
Perez, E.A.1
-
74
-
-
70350604328
-
Optimal use of taxanes in metastatic breast cancer
-
King KM, Lupichuk S, Baig L, et al. Optimal use of taxanes in metastatic breast cancer. Journal 2009;16:8-20
-
(2009)
Journal
, vol.16
, pp. 8-20
-
-
King, K.M.1
Lupichuk, S.2
Baig, L.3
-
75
-
-
0033767619
-
Risks and benefits of taxanes in breast and ovarian cancer
-
Michaud LB, Valero V, Hortobagyi G. Risks and benefits of taxanes in breast and ovarian cancer. Drug Saf 2000;23:401
-
(2000)
Drug Saf.
, vol.23
, pp. 401
-
-
Michaud, L.B.1
Valero, V.2
Hortobagyi, G.3
-
76
-
-
33646734282
-
Taxanes in the treatment of non-small cell lung cancer
-
Fanucchi M, Khuri FR. Taxanes in the treatment of non-small cell lung cancer. Treat Res Med 2006;5:181-91
-
(2006)
Treat Res. Med.
, vol.5
, pp. 181-191
-
-
Fanucchi, M.1
Khuri, F.R.2
-
78
-
-
56949084877
-
Albumin as a drug carrier: Design of prodrugs, drug conjugates and nanoparticles
-
Kratz F. Albumin as a drug carrier: Design of prodrugs, drug conjugates and nanoparticles. J Control Release 2008;132:171-83
-
(2008)
J. Control Release
, vol.132
, pp. 171-183
-
-
Kratz, F.1
-
79
-
-
33845798299
-
Nanoemulsions as versatile formulations for paclitaxel delivery: Peroral and dermal delivery studies in rats
-
Khandavilli S, Panchagnula R. Nanoemulsions as versatile formulations for paclitaxel delivery: Peroral and dermal delivery studies in rats. J Investig Dermatol 2007;127:154-62
-
(2007)
J. Investig Dermatol.
, vol.127
, pp. 154-162
-
-
Khandavilli, S.1
Panchagnula, R.2
-
80
-
-
0344975483
-
Effects of DDD on steroid response and blood flow through the adrenal after ACTH
-
Nichols J, Richardson A. Effects of DDD on steroid response and blood flow through the adrenal after ACTH. Proc Soc Exp Biol Med 1960;104:539-42
-
(1960)
Proc. Soc. Exp. Biol. Med.
, vol.104
, pp. 539-542
-
-
Nichols, J.1
Richardson, A.2
-
81
-
-
53149141892
-
Cushing's syndrome due to adrenocortical hyperplasia treatment with an inhibitor of adrenocortical secretions
-
Wallace E, Silverstein J, Villadolid L, et al. Cushing's syndrome due to adrenocortical hyperplasia. Treatment with an inhibitor of adrenocortical secretions. N Engl J Med 1961;265:1088-93
-
(1961)
N. Engl. J. Med.
, vol.265
, pp. 1088-1093
-
-
Wallace, E.1
Silverstein, J.2
Villadolid, L.3
-
82
-
-
79960525593
-
Place du mitotane dans la prise en charge du carcinome corticosurrenalien
-
Attivi D, Gibaud S. Place du mitotane dans la prise en charge du carcinome corticosurrenalien. Act Pharm Hosp 2011;7:39-41
-
(2011)
Act. Pharm. Hosp.
, vol.7
, pp. 39-41
-
-
Attivi, D.1
Gibaud, S.2
-
84
-
-
0034605692
-
Colloidal carriers for benzathine penicillin G: Nanoemulsions and nanocapsules
-
Santos-Magalhaes NS, Pontes A, Pereira VM, et al. Colloidal carriers for benzathine penicillin G: Nanoemulsions and nanocapsules. Int J Pharm 2000;208:71-80
-
(2000)
Int. J. Pharm.
, vol.208
, pp. 71-80
-
-
Santos-Magalhaes, N.S.1
Pontes, A.2
Pereira, V.M.3
-
85
-
-
23844542459
-
Effect of solubilizing and microemulsifying excipients in polyethylene glycol 6000 solid dispersion on enhanced dissolution and bioavailability of ketoconazole
-
Heo M, Piao Z, Kim T, et al. Effect of solubilizing and microemulsifying excipients in polyethylene glycol 6000 solid dispersion on enhanced dissolution and bioavailability of ketoconazole. Arch Pharm Res 2005;28:604-11
-
(2005)
Arch. Pharm. Res.
, vol.28
, pp. 604-611
-
-
Heo, M.1
Piao, Z.2
Kim, T.3
-
86
-
-
48249121084
-
Preparation and evaluation of a microemulsion for oral delivery of berberine
-
Gui S-Y, Wu L, Peng DY, et al. Preparation and evaluation of a microemulsion for oral delivery of berberine. Pharmazie 2008;63:516-19
-
(2008)
Pharmazie
, vol.63
, pp. 516-519
-
-
Gui, S.-Y.1
Wu, L.2
Peng, D.Y.3
-
87
-
-
0030877505
-
Focus on carvedilol: A novel beta-adrenergic blocking agent for the treatment of congestive heart failure
-
Chen B, Chow M. Focus on carvedilol: A novel beta-adrenergic blocking agent for the treatment of congestive heart failure. Formulary 1997;32:795-805
-
(1997)
Formulary
, vol.32
, pp. 795-805
-
-
Chen, B.1
Chow, M.2
-
88
-
-
0028271342
-
Clinical pharmacokinetics and pharmacodynamics of carvedilol
-
Morgan T. Clinical pharmacokinetics and pharmacodynamics of carvedilol. Clin Pharmacokinet 1994;26:335-46
-
(1994)
Clin. Pharmacokinet.
, vol.26
, pp. 335-346
-
-
Morgan, T.1
-
90
-
-
25144440877
-
Preparation and evaluation of SEDDS and SMEDDS containing carvedilol
-
Wei L, Sun P, Nie S, et al. Preparation and evaluation of SEDDS and SMEDDS containing carvedilol. Drug Dev Ind Pharm 2005;31:785-94
-
(2005)
Drug Dev. Ind. Pharm.
, vol.31
, pp. 785-794
-
-
Wei, L.1
Sun, P.2
Nie, S.3
-
91
-
-
84862548012
-
Pharmacokinetic comparison of a single oral dose of polymorph form I versus form V capsules of the anti-Orthopoxvirus compound ST-246(R) in human volunteers
-
Epub ahead of print
-
Chinsangaram J, Honeychurch KM, Tyavanagimatt SR, et al. Pharmacokinetic comparison of a single oral dose of polymorph form I versus form V capsules of the anti-orthopoxvirus compound ST-246(R) in human volunteers. Antimicrob Agents Chemother 2012. [Epub ahead of print]
-
(2012)
Antimicrob. Agents Chemother.
-
-
Chinsangaram, J.1
Honeychurch, K.M.2
Tyavanagimatt, S.R.3
-
92
-
-
25144495111
-
Enhanced oral bioavailability of ibuprofen in rats by poloxamer gel using poloxamer 188 and menthol
-
Yong CS, Lee M-K, Park Y-J, et al. Enhanced oral bioavailability of ibuprofen in rats by poloxamer gel using poloxamer 188 and menthol. Drug Dev Ind Pharm 2005;31:615-22
-
(2005)
Drug Dev. Ind. Pharm.
, vol.31
, pp. 615-622
-
-
Yong, C.S.1
Lee, M.-K.2
Park, Y.-J.3
-
93
-
-
84864241991
-
Enhancement of oral bioavailability and solid dispersion: A review
-
Saffoon N, Uddin R, Huda NH, et al. Enhancement of oral bioavailability and solid dispersion: A review. J Appl Pharm Sci 2011;1:13-20
-
(2011)
J. Appl. Pharm. Sci.
, vol.1
, pp. 13-20
-
-
Saffoon, N.1
Uddin, R.2
Huda, N.H.3
-
94
-
-
0034601240
-
Improving drug solubility for oral delivery using solid dispersions
-
Leuner C, Dressman J. Improving drug solubility for oral delivery using solid dispersions. Eur J Pharm Biopharm 2000;50:47-60
-
(2000)
Eur. J. Pharm. Biopharm.
, vol.50
, pp. 47-60
-
-
Leuner, C.1
Dressman, J.2
-
95
-
-
84859719708
-
Oral drug delivery with polymeric nanoparticles: The gastrointestinal mucus barriers
-
Ensign LM, Cone R, Hanes J. Oral drug delivery with polymeric nanoparticles: The gastrointestinal mucus barriers. Adv Drug Deliv Rev 2012;64:557-70
-
(2012)
Adv. Drug Deliv. Rev.
, Issue.64
, pp. 557-570
-
-
Ensign, L.M.1
Cone, R.2
Hanes, J.3
-
96
-
-
2942702257
-
Issues in oral nanoparticle drug carrier uptake and targeting
-
Florence AT. Issues in oral nanoparticle drug carrier uptake and targeting. J Drug Target 2004;12:65-70
-
(2004)
J. Drug Target
, vol.12
, pp. 65-70
-
-
Florence, A.T.1
-
97
-
-
33744974493
-
Enhancement of the dissolution rate and oral absorption of a poorly water soluble drug by formation of surfactant-containing microparticles
-
Wong S, Kellaway I, Murdan S. Enhancement of the dissolution rate and oral absorption of a poorly water soluble drug by formation of surfactant-containing microparticles. Int J Pharm 2006;317:61-8
-
(2006)
Int. J. Pharm.
, vol.317
, pp. 61-68
-
-
Wong, S.1
Kellaway, I.2
Murdan, S.3
-
98
-
-
0035937599
-
Nanosuspensions as particulate drug formulations in therapy: Rationale for development and what we can expect for the future
-
Muller R, Jacobs C, Kayser O. Nanosuspensions as particulate drug formulations in therapy: Rationale for development and what we can expect for the future. Adv Drug Deliv Rev 2001;47:3-19
-
(2001)
Adv. Drug Deliv. Rev.
, vol.47
, pp. 3-19
-
-
Muller, R.1
Jacobs, C.2
Kayser, O.3
-
99
-
-
79957948653
-
The use of cyclodextrins nanoparticles for oral delivery
-
Kanwar JR, Long BM, Kanwar RK. The use of cyclodextrins nanoparticles for oral delivery. Curr Med Chem 2011;18:2079-85
-
(2011)
Curr. Med. Chem.
, vol.18
, pp. 2079-2085
-
-
Kanwar, J.R.1
Long, B.M.2
Kanwar, R.K.3
-
100
-
-
79955962787
-
Strategies to improve dissolution and oral absorption of glimepiride tablets: Solid dispersion versus micronization techniques
-
Ning X, Sun J, Han X, et al. Strategies to improve dissolution and oral absorption of glimepiride tablets: Solid dispersion versus micronization techniques. Drug Dev Ind Pharm 2011;37:727-36
-
(2011)
Drug Dev. Ind. Pharm.
, vol.37
, pp. 727-736
-
-
Ning, X.1
Sun, J.2
Han, X.3
-
101
-
-
3242673239
-
PH-sensitive nanoparticles for improving the oral bioavailability of cyclosporine A
-
Dai J, Nagai T, Wang X, et al. pH-sensitive nanoparticles for improving the oral bioavailability of cyclosporine A. Int J Pharm 2004;280:229-40
-
(2004)
Int. J. Pharm.
, vol.280
, pp. 229-240
-
-
Dai, J.1
Nagai, T.2
Wang, X.3
-
102
-
-
3042551382
-
Bioavailability and pharmacokinetics of cyclosporine A-loaded pH-sensitive nanoparticles for oral administration
-
Wang X, Dai J, Chen Z, et al. Bioavailability and pharmacokinetics of cyclosporine A-loaded pH-sensitive nanoparticles for oral administration. J Control Release 2004;97:421-9
-
(2004)
J. Control Release
, vol.97
, pp. 421-429
-
-
Wang, X.1
Dai, J.2
Chen, Z.3
-
103
-
-
34249087392
-
PLGA nanoparticles for oral delivery of cyclosporine: Nephrotoxicity and pharmacokinetic studies in comparison to Sandimmun Neoral
-
Italia J, Bhatt D, Bhardwaj V, et al. PLGA nanoparticles for oral delivery of cyclosporine: Nephrotoxicity and pharmacokinetic studies in comparison to Sandimmun Neoral-.. J Control Release 2007;119:197-206
-
(2007)
J. Control Release
, vol.119
, pp. 197-206
-
-
Italia, J.1
Bhatt, D.2
Bhardwaj, V.3
-
104
-
-
0037027833
-
Positively charged nanoparticles for improving the oral bioavailability of cyclosporin-A
-
El-Shabouri M. Positively charged nanoparticles for improving the oral bioavailability of cyclosporin-A. Int J Pharm 2002;249:101-8
-
(2002)
Int. J. Pharm.
, vol.249
, pp. 101-108
-
-
El-Shabouri, M.1
-
105
-
-
33744973517
-
Oral bioavailability of cyclosporine: Solid lipid nanoparticles (SLN-) versus drug nanocrystals
-
Muller RH, Runge S, Ravelli V, et al. Oral bioavailability of cyclosporine: Solid lipid nanoparticles (SLN) versus drug nanocrystals. Int J Pharm 2006;317:82-9
-
(2006)
Int. J. Pharm.
, vol.317
, pp. 82-89
-
-
Muller, R.H.1
Runge, S.2
Ravelli, V.3
-
106
-
-
77951189574
-
Pharmacokinetics and enhanced oral bioavailability in beagle dogs of cyclosporine A encapsulated in glyceryl monooleate/poloxamer 407 cubic nanoparticles
-
Lai J, Lu Y, Yin Z, et al. Pharmacokinetics and enhanced oral bioavailability in beagle dogs of cyclosporine A encapsulated in glyceryl monooleate/poloxamer 407 cubic nanoparticles. Int J Nanomed 2010;5:13-23
-
(2010)
Int. J. Nanomed.
, vol.5
, pp. 13-23
-
-
Lai, J.1
Lu, Y.2
Yin, Z.3
-
107
-
-
77955758519
-
Nanoparticles made of multi-block copolymer of lactic acid and ethylene glycol containing periodic side-chain carboxyl groups for oral delivery of cyclosporine A
-
Ankola DD, Battisti A, Solaro R, et al. Nanoparticles made of multi-block copolymer of lactic acid and ethylene glycol containing periodic side-chain carboxyl groups for oral delivery of cyclosporine A. J R Soc Interface 2010;7(Suppl 4):S475-81
-
(2010)
J. R Soc. Interface
, vol.7
, Issue.SUPPL.4
-
-
Ankola, D.D.1
Battisti, A.2
Solaro, R.3
-
108
-
-
23644450237
-
Polymeric micelles for the solubilization and delivery of cyclosporine A: Pharmacokinetics and biodistribution
-
Aliabadi HM, Brocks DR, Lavasanifar A. Polymeric micelles for the solubilization and delivery of cyclosporine A: Pharmacokinetics and biodistribution. Biomaterials 2005;26:7251-9
-
(2005)
Biomaterials
, vol.26
, pp. 7251-7259
-
-
Aliabadi, H.M.1
Brocks, D.R.2
Lavasanifar, A.3
-
109
-
-
11244324046
-
Solubilization and pharmacokinetic behaviors of sodium cholate/lecithinmixed micelles containing cyclosporine A
-
Guo J, Wu T, Ping Q, et al. Solubilization and pharmacokinetic behaviors of sodium cholate/lecithinmixed micelles containing cyclosporine A. Drug Deliv 2005;12:35-9
-
(2005)
Drug Deliv.
, vol.12
, pp. 35-39
-
-
Guo, J.1
Wu, T.2
Ping, Q.3
-
110
-
-
0035821352
-
Bioavailability of cyclosporin A dispersed in sodium lauryl sulfate-dextrin based solid microspheres
-
Lee E, Lee S, Choi H, et al. Bioavailability of cyclosporin A dispersed in sodium lauryl sulfate-dextrin based solid microspheres. Int J Pharm 2001;218:125-31
-
(2001)
Int. J. Pharm.
, vol.218
, pp. 125-131
-
-
Lee, E.1
Lee, S.2
Choi, H.3
-
111
-
-
0035937507
-
Pharmacokinetic behavior of cyclosporin A in rabbits by oral administration of lecithin vesicle and Sandimmun Neoral
-
Guo J, Ping Q, Chen Y. Pharmacokinetic behavior of cyclosporin A in rabbits by oral administration of lecithin vesicle and Sandimmun Neoral. Int J Pharm 2001;216:17-21
-
(2001)
Int. J. Pharm.
, vol.216
, pp. 17-21
-
-
Guo, J.1
Ping, Q.2
Chen, Y.3
-
112
-
-
33750069158
-
Preparation, characterization and in vivo studies of proliposomes containing Cyclosporine A
-
Shah NM, Parikh J, Namdeo A, et al. Preparation, characterization and in vivo studies of proliposomes containing Cyclosporine A. J Nanosci Nanotechnol 2006;6:2967-73
-
(2006)
J. Nanosci. Nanotechnol.
, vol.6
, pp. 2967-2973
-
-
Shah, N.M.1
Parikh, J.2
Namdeo, A.3
-
113
-
-
32344439711
-
Enhancing the bioavailability of cyclosporine a using solid dispersion containing polyoxyethylene 40) stearate
-
Liu C, Wu J, Shi B, et al. Enhancing the bioavailability of cyclosporine a using solid dispersion containing polyoxyethylene (40) stearate. Drug Dev Ind Pharm 2006;32:115-23
-
(2006)
Drug Dev. Ind. Pharm.
, Issue.32
, pp. 115-123
-
-
Liu, C.1
Wu, J.2
Shi, B.3
-
114
-
-
23244462957
-
Elevating Bioavailability of cyclosporine A via encapsulation in artificial oil bodies stabilized by caleosin
-
Chen M, Wang J, Tzen J. Elevating Bioavailability of cyclosporine A via encapsulation in artificial oil bodies stabilized by caleosin. Biotech Prog 2005;21:1297-301
-
(2005)
Biotech. Prog.
, vol.21
, pp. 1297-1301
-
-
Chen, M.1
Wang, J.2
Tzen, J.3
-
115
-
-
78650159620
-
Preparation and evaluation of ibuprofen-loaded microemulsion for improvement of oral bioavailability
-
Hu L, Yang J, Liu W, et al. Preparation and evaluation of ibuprofen-loaded microemulsion for improvement of oral bioavailability. Drug Deliv 2011;18:90-5
-
(2011)
Drug Deliv.
, vol.18
, pp. 90-95
-
-
Hu, L.1
Yang, J.2
Liu, W.3
-
116
-
-
75549088044
-
Microemulsion system with improved loading of piroxicam: A study of microstructure
-
Nazar MF, Khan AM, Shah SS. Microemulsion system with improved loading of piroxicam: A study of microstructure. AAPS PharmSciTech 2009;10:1286-94
-
(2009)
AAPS Pharm. Sci. Tech.
, vol.10
, pp. 1286-1294
-
-
Nazar, M.F.1
Khan, A.M.2
Shah, S.S.3
-
117
-
-
29244491192
-
Decrease of genital organ weights and plasma testosterone levels in rats following oral administration of leuprolide microemulsion
-
Zheng JY, Fulu M-Y. Decrease of genital organ weights and plasma testosterone levels in rats following oral administration of leuprolide microemulsion. Int J Pharm 2006;307:209-15
-
(2006)
Int. J. Pharm.
, vol.307
, pp. 209-215
-
-
Zheng, J.Y.1
Fulu, M.-Y.2
-
118
-
-
84864189372
-
Design and development of microemulsion drug delivery system of nifedipine for improvement of oral bioavailability
-
Gupta A. Design and development of microemulsion drug delivery system of nifedipine for improvement of oral bioavailability. Res J Pharm Sci Biotech 2011;1:51-6
-
(2011)
Res. J. Pharm. Sci. Biotech.
, vol.1
, pp. 51-56
-
-
Gupta, A.1
-
119
-
-
0035984949
-
Lipid-based formulations for intestinal lymphatic delivery
-
O'Driscoll CM. Lipid-based formulations for intestinal lymphatic delivery. Eur J Pharm Sci 2002;15:405-15
-
(2002)
Eur. J. Pharm. Sci.
, vol.15
, pp. 405-415
-
-
O'Driscoll, C.M.1
|