-
1
-
-
0030712909
-
Improved oral bioavailability of the hypocholesterolemic DMP 565 in dogs following oral dosing in oil and glycol solutions
-
D. L. Burcham, M. B. Maurin, E. A. Hausner and S. M. Huang, Improved oral bioavailability of the hypocholesterolemic DMP 565 in dogs following oral dosing in oil and glycol solutions, Biopharm. Drug Dispos. 18 (1997) 737-742.
-
(1997)
Biopharm. Drug Dispos
, vol.18
, pp. 737-742
-
-
Burcham, D.L.1
Maurin, M.B.2
Hausner, E.A.3
Huang, S.M.4
-
2
-
-
0024218073
-
Effect of vehicle amphiphilicity on the dissolution and bioavailability of a poorly water-soluble drug from solid dispersion
-
A. T. M. Serajuddin, P. C. Sheen, D. Mufson, D. F. Bernstein and M. A. Augustine, Effect of vehicle amphiphilicity on the dissolution and bioavailability of a poorly water-soluble drug from solid dispersion, J. Pharm. Sci. 77 (1988) 414-417.
-
(1988)
J. Pharm. Sci
, vol.77
, pp. 414-417
-
-
Serajuddin, A.T.M.1
Sheen, P.C.2
Mufson, D.3
Bernstein, D.F.4
Augustine, M.A.5
-
3
-
-
0026809853
-
Systemic bioavailability of penclomedine (NSC-338720) from oil-in-water emulsions administered intraduodenally to rats
-
R. A. Myers and V. J. Stella, Systemic bioavailability of penclomedine (NSC-338720) from oil-in-water emulsions administered intraduodenally to rats, Int. J. Pharm. 78 (1992) 217-226.
-
(1992)
Int. J. Pharm
, vol.78
, pp. 217-226
-
-
Myers, R.A.1
Stella, V.J.2
-
4
-
-
0029806234
-
Lipophilic 1-beta-d-arabino-furanosyl cytosine derivatives in liposomal formulations for oral and parenteral antileukemic therapy in the murine L1210 leukemia model
-
R. A. Schwendener and H. Schott, Lipophilic 1-beta-d-arabino-furanosyl cytosine derivatives in liposomal formulations for oral and parenteral antileukemic therapy in the murine L1210 leukemia model, J. Cancer Res. Clin. Oncol. 122 (1996) 723-726.
-
(1996)
J. Cancer Res. Clin. Oncol
, vol.122
, pp. 723-726
-
-
Schwendener, R.A.1
Schott, H.2
-
5
-
-
0026586447
-
Self-emulsifying drug delivery systems: Formulation and biopharmaceutical evaluation of an investigational lipophilic compound
-
S. A. Charman, W. N. Charman, M. C. Rogge, T. D. Wilson and C. W. Pouton, Self-emulsifying drug delivery systems: formulation and biopharmaceutical evaluation of an investigational lipophilic compound, Pharm. Res. 9 (1992) 83-87.
-
(1992)
Pharm. Res
, vol.9
, pp. 83-87
-
-
Charman, S.A.1
Charman, W.N.2
Rogge, M.C.3
Wilson, T.D.4
Pouton, C.W.5
-
6
-
-
0022366625
-
SEDDS: Assessment of the efficiency of emulsification
-
C. W. Pouton, SEDDS: Assessment of the efficiency of emulsification, Int. J. Pharm. 27 (1985) 335-348.
-
(1985)
Int. J. Pharm
, vol.27
, pp. 335-348
-
-
Pouton, C.W.1
-
7
-
-
0028194817
-
Self-emulsifying drug delivery systems (SEDDS) with polyglycolyzed glycerides for improving in vitro dissolution and oral absorption of lipophilic drugs
-
N. H. Shah, M. T. Carvajal, C. I. Patel, N. H. Infeld and A. W. Malick, Self-emulsifying drug delivery systems (SEDDS) with polyglycolyzed glycerides for improving in vitro dissolution and oral absorption of lipophilic drugs, Int. J. Pharm. 106 (1994) 15-23.
-
(1994)
Int. J. Pharm
, vol.106
, pp. 15-23
-
-
Shah, N.H.1
Carvajal, M.T.2
Patel, C.I.3
Infeld, N.H.4
Malick, A.W.5
-
8
-
-
0035895309
-
Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10: Formulation development and bioavailability assessment
-
T. R. Kommuru, B. Gurley, M. A. Khan and I. K. Reddy, Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10: formulation development and bioavailability assessment, Int. J. Pharm. 212 (2001) 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
-
9
-
-
0343963156
-
Improved bioavailability of vitamin E with a self-emulsifying formulation
-
T. Julianto, K. H. Yuen and A. M. Noor, Improved bioavailability of vitamin E with a self-emulsifying formulation, Int. J. Pharm. 200 (2000) 53-57.
-
(2000)
Int. J. Pharm
, vol.200
, pp. 53-57
-
-
Julianto, T.1
Yuen, K.H.2
Noor, A.M.3
-
10
-
-
0032103706
-
Formulation design and bioavailability assessment of lipidic self-emulsifying formulations of halofantrine
-
S. M. Khoo, A. J. Humberstone, C. J. H. Porter, G. A. Edwards and W. N. Charman, Formulation design and bioavailability assessment of lipidic self-emulsifying formulations of halofantrine, Int. J. Pharm. 167 (1998) 155-164.
-
(1998)
Int. J. Pharm
, vol.167
, pp. 155-164
-
-
Khoo, S.M.1
Humberstone, A.J.2
Porter, C.J.H.3
Edwards, G.A.4
Charman, W.N.5
-
11
-
-
0032498581
-
Physicochemical characterization and evaluation of a microemulsion system for oral delivery of cyclosporine A
-
Z. G. Gao, H. G. Choi, H. J. Shin, K. M. Park, S. J. Lim, K. J. Hwang and C. K. Kim, Physicochemical characterization and evaluation of a microemulsion system for oral delivery of cyclosporine A, Int. J. Pharm. 161 (1998) 75-86.
-
(1998)
Int. J. Pharm
, vol.161
, pp. 75-86
-
-
Gao, Z.G.1
Choi, H.G.2
Shin, H.J.3
Park, K.M.4
Lim, S.J.5
Hwang, K.J.6
Kim, C.K.7
-
12
-
-
0343487750
-
Formulation of self-emulsifying drug delivery systems
-
C. W. Pouton, Formulation of self-emulsifying drug delivery systems, Adv. Drug Deliv. Rev. 25 (1997) 47-58.
-
(1997)
Adv. Drug Deliv. Rev
, vol.25
, pp. 47-58
-
-
Pouton, C.W.1
-
13
-
-
0031038268
-
The potential of oily formulations for drug delivery to the gastro-intestinal tract
-
C. W. Pouton and W. N. Charman, The potential of oily formulations for drug delivery to the gastro-intestinal tract, Adv. Drug Deliv. Rev. 25 (1997) 1-2.
-
(1997)
Adv. Drug Deliv. Rev
, vol.25
, pp. 1-2
-
-
Pouton, C.W.1
Charman, W.N.2
-
14
-
-
1842609789
-
Development of self-microemulsifying drug delivery system for oral availability enhancement of simvastatin in beagle dogs
-
B. K. Kang, J. S. Lee, S. K. Chon, S. Y. Jeong, S. H. Yuk, G. Khang, H. B. Lee and S. H. Cho, Development of self-microemulsifying drug delivery system for oral availability enhancement of simvastatin in beagle dogs, Int. J. Pharm. 274 (2005) 65-73.
-
(2005)
Int. J. Pharm
, vol.274
, 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
-
15
-
-
0025853030
-
Enhancement of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitor efficacy through administration of a controlled-porosity osmotic pump dosage form
-
C. A. McClelland, R. J. Stubbs, J. A. Fix, S. A. Pogany and G. M. Zentner, Enhancement of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitor efficacy through administration of a controlled-porosity osmotic pump dosage form, Pharm. Res. 8 (1991) 873-876.
-
(1991)
Pharm. Res
, vol.8
, pp. 873-876
-
-
McClelland, C.A.1
Stubbs, R.J.2
Fix, J.A.3
Pogany, S.A.4
Zentner, G.M.5
-
16
-
-
0027435363
-
Evaluation of sustained/controlled-release dosage forms of 3-hydroxy-3- methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors in dogs and humans
-
H. Cheng, S. C. Sutton, J. D. Pipkin, G. M. Zentner, J. D. Rogers, J. I. Schwartz, Y. B. Mitchel, K. Grasing, M. S. Schwartz, R. D. L. Amin, Liu, D. L. Ebel, A. Coulter, K. Engle, G. A. McClelland, C. Y. Lui and G. S. Rork, Evaluation of sustained/controlled-release dosage forms of 3-hydroxy-3- methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors in dogs and humans, Pharm. Res. 10 (1993) 1683-1687.
-
(1993)
Pharm. Res
, vol.10
, pp. 1683-1687
-
-
Cheng, H.1
Sutton, S.C.2
Pipkin, J.D.3
Zentner, G.M.4
Rogers, J.D.5
Schwartz, J.I.6
Mitchel, Y.B.7
Grasing, K.8
Schwartz, M.S.9
Amin, R.D.L.10
Liu11
Ebel, D.L.12
Coulter, A.13
Engle, K.14
McClelland, G.A.15
Lui, C.Y.16
Rork, G.S.17
-
17
-
-
21244445440
-
Spray dried amorphous solid dispersions of simvastatin; a low Tg drug: In vitro and in vivo evaluations
-
A. A. Ambike, K. R. Mahadik and A. Paradkar, Spray dried amorphous solid dispersions of simvastatin; a low Tg drug: In vitro and in vivo evaluations, Pharm. Res. 22 (2005) 990-998.
-
(2005)
Pharm. Res
, vol.22
, pp. 990-998
-
-
Ambike, A.A.1
Mahadik, K.R.2
Paradkar, A.3
-
18
-
-
85176869039
-
-
USP Convention, Rockville
-
USP 24/NF 19, USP Convention, Rockville 2000, pp. 1942.
-
(2000)
USP 24/NF 19
, pp. 1942
-
-
-
20
-
-
23144432623
-
Effect of formulation variables on preparation and evaluation of gelled self-emulsifying drug delivery system of ketoprofen
-
P. Patil, P. Joshi and A. Paradkar, Effect of formulation variables on preparation and evaluation of gelled self-emulsifying drug delivery system of ketoprofen, AAPS Pharm. Sci. Tech. 5 (2004) 1-8.
-
(2004)
AAPS Pharm. Sci. Tech
, vol.5
, pp. 1-8
-
-
Patil, P.1
Joshi, P.2
Paradkar, A.3
-
21
-
-
0343673791
-
Preparation and in vitro evaluation of self-microemulsifying drug delivery systems containing idebenone
-
H. J. Kim, K. A. Yoon, M. Hahn, E. S. Park and S. C. Chi, Preparation and in vitro evaluation of self-microemulsifying drug delivery systems containing idebenone, Drug Dev. Ind. Pharm. 26 (2000) 523-529.
-
(2000)
Drug Dev. Ind. Pharm
, vol.26
, pp. 523-529
-
-
Kim, H.J.1
Yoon, K.A.2
Hahn, M.3
Park, E.S.4
Chi, S.C.5
-
23
-
-
0026488868
-
Tropical oils: Nutritional and scientific issues
-
C. E. Elson, Tropical oils: nutritional and scientific issues, Crit. Rev. Food Sci. Nutr. 31 (1992) 79-102.
-
(1992)
Crit. Rev. Food Sci. Nutr
, vol.31
, pp. 79-102
-
-
Elson, C.E.1
-
24
-
-
0343488673
-
Intestinal secretion of drugs. The role of P-glycoprotein and related drug efflux systems in limiting oral absorption
-
J. Hunter and B. H. Hirst, Intestinal secretion of drugs. The role of P-glycoprotein and related drug efflux systems in limiting oral absorption, Adv. Drug Del. Rev. 25 (1997) 129-157.
-
(1997)
Adv. Drug Del. Rev
, vol.25
, pp. 129-157
-
-
Hunter, J.1
Hirst, B.H.2
|