-
1
-
-
0028948839
-
A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability
-
Amidon G.L., Lennernas H., Shah V.P., and Crison J.R. A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm. Res. 12 (1995) 413-420
-
(1995)
Pharm. Res.
, vol.12
, pp. 413-420
-
-
Amidon, G.L.1
Lennernas, H.2
Shah, V.P.3
Crison, J.R.4
-
2
-
-
0036805875
-
Improved oral bioavailability of cyclosporin A in male Wistar rats. Comparison of a Solutol HS 15 containing self-dispersing formulation and a microsuspension
-
Bravo Gonzalez R.C., Huwyler J., Walter I., Mountfield R., and Bittner B. Improved oral bioavailability of cyclosporin A in male Wistar rats. Comparison of a Solutol HS 15 containing self-dispersing formulation and a microsuspension. Int. J. Pharm. 245 (2002) 143-151
-
(2002)
Int. J. Pharm.
, vol.245
, pp. 143-151
-
-
Bravo Gonzalez, R.C.1
Huwyler, J.2
Walter, I.3
Mountfield, R.4
Bittner, B.5
-
3
-
-
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 S.M., Charman W.N., and Porter C.J. 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. 89 (2000) 1073-1084
-
(2000)
J. Pharm. Sci.
, vol.89
, pp. 1073-1084
-
-
Caliph, S.M.1
Charman, W.N.2
Porter, C.J.3
-
4
-
-
0026586447
-
Self-emulsifying drug delivery systems: formulation and biopharmaceutic evaluation of an investigational lipophilic compound
-
Charman S.A., Charman W.N., Rogge M.C., Wilson T.D., Dutko F.J., and Pouton C.W. Self-emulsifying drug delivery systems: formulation and biopharmaceutic evaluation of an investigational lipophilic compound. Pharm. Res. 9 (1992) 87-93
-
(1992)
Pharm. Res.
, vol.9
, 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
-
5
-
-
0029562489
-
Lipid microemulsions for improving drug dissolution and oral absorption: physical and biopharmaceutical aspects
-
Constantinides P.P. Lipid microemulsions for improving drug dissolution and oral absorption: physical and biopharmaceutical aspects. Pharm. Res. 12 (1995) 1561-1572
-
(1995)
Pharm. Res.
, vol.12
, pp. 1561-1572
-
-
Constantinides, P.P.1
-
6
-
-
0347022226
-
Intestinal absorption of penclomedine from lipid vehicles in the conscious rat: contribution of emulsification versus digestibility
-
de Smidt P.C., Campanero M.A., and Troconiz I.F. Intestinal absorption of penclomedine from lipid vehicles in the conscious rat: contribution of emulsification versus digestibility. Int. J. Pharm. 270 (2004) 109-118
-
(2004)
Int. J. Pharm.
, vol.270
, pp. 109-118
-
-
de Smidt, P.C.1
Campanero, M.A.2
Troconiz, I.F.3
-
7
-
-
0025096728
-
Medium-chain versus long-chain triacylglycerol emulsion hydrolysis by lipoprotein lipase and hepatic lipase: implications for the mechanisms of lipase action
-
Deckelbaum R.J., Hamilton J.A., Moser A., Bengtsson-Olivecrona G., Butbul E., Carpentier Y.A., Gutman A., and Olivecrona T. Medium-chain versus long-chain triacylglycerol emulsion hydrolysis by lipoprotein lipase and hepatic lipase: implications for the mechanisms of lipase action. Biochemistry 29 (1990) 1136-1142
-
(1990)
Biochemistry
, vol.29
, pp. 1136-1142
-
-
Deckelbaum, R.J.1
Hamilton, J.A.2
Moser, A.3
Bengtsson-Olivecrona, G.4
Butbul, E.5
Carpentier, Y.A.6
Gutman, A.7
Olivecrona, T.8
-
8
-
-
0034601204
-
Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs
-
Gershanik T., and Benita S. Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs. Eur. J. Pharm. Biopharm. 50 (2000) 179-188
-
(2000)
Eur. J. Pharm. Biopharm.
, vol.50
, pp. 179-188
-
-
Gershanik, T.1
Benita, S.2
-
9
-
-
25444464372
-
Bioavailability of seocalcitol. I. Relating solubility in biorelevant media with oral bioavailability in rats-effect of medium and long chain triglycerides
-
Grove M., Pedersen G.P., Nielsen J.L., and Mullertz A. Bioavailability of seocalcitol. I. Relating solubility in biorelevant media with oral bioavailability in rats-effect of medium and long chain triglycerides. J. Pharm. Sci. 94 (2005) 1830-1838
-
(2005)
J. Pharm. Sci.
, vol.94
, pp. 1830-1838
-
-
Grove, M.1
Pedersen, G.P.2
Nielsen, J.L.3
Mullertz, A.4
-
10
-
-
0344443710
-
Excipient effects on in vitro cytotoxicity of a novel paclitaxel self-emulsifying drug delivery system
-
Gursoy N., Garrigue J.S., Razafindratsita A., Lambert G., and Benita S. Excipient effects on in vitro cytotoxicity of a novel paclitaxel self-emulsifying drug delivery system. J. Pharm. Sci. 92 (2003) 2411-2418
-
(2003)
J. Pharm. Sci.
, vol.92
, pp. 2411-2418
-
-
Gursoy, N.1
Garrigue, J.S.2
Razafindratsita, A.3
Lambert, G.4
Benita, S.5
-
11
-
-
1842684453
-
Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs
-
Gursoy R.N., and Benita S. Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs. Biomed. Pharmacother. 58 (2004) 173-182
-
(2004)
Biomed. Pharmacother.
, vol.58
, pp. 173-182
-
-
Gursoy, R.N.1
Benita, S.2
-
12
-
-
0031914282
-
Lipid-based delivery systems for improving the bioavailability and lymphatic transport of a poorly water-soluble LTB4 inhibitor
-
Hauss D.J., Fogal S.E., Ficorilli J.V., Price C.A., Roy T., Jayaraj A.A., and Keirns J.J. Lipid-based delivery systems for improving the bioavailability and lymphatic transport of a poorly water-soluble LTB4 inhibitor. J. Pharm. Sci. 87 (1998) 164-169
-
(1998)
J. Pharm. Sci.
, vol.87
, 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
-
13
-
-
0342617694
-
Lipid-based vehicles for the oral delivery of poorly water soluble drugs
-
Humberstone A.J., and Charman W.N. Lipid-based vehicles for the oral delivery of poorly water soluble drugs. Adv. Drug Deliv. Rev. 25 (1997) 103-128
-
(1997)
Adv. Drug Deliv. Rev.
, vol.25
, pp. 103-128
-
-
Humberstone, A.J.1
Charman, W.N.2
-
14
-
-
0343963156
-
Improved bioavailability of vitamin E with a self emulsifying formulation
-
Julianto T., Yuen K.H., and Noor A.M. 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
-
15
-
-
1842609789
-
Development of self-microemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogs
-
Kang B.K., Lee J.S., Chon S.K., Jeong S.Y., Yuk S.H., Khang G., Lee H.B., and Cho S.H. Development of self-microemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogs. Int. J. Pharm. 274 (2004) 65-73
-
(2004)
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
-
16
-
-
0032103706
-
Formulation design and bioavailability assessment of lipidic self-emulsifying formulations of halofantrine
-
Khoo S.M., Humberstone A.J., Porter C.J., Edwards G.A., and Charman W.N. 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.3
Edwards, G.A.4
Charman, W.N.5
-
17
-
-
0033992180
-
Enhanced absorption of indomethacin after oral or rectal administration of self-emulsifying system containing indomethacin to rats
-
Kim J.Y., and Ku Y.S. Enhanced absorption of indomethacin after oral or rectal administration of self-emulsifying system containing indomethacin to rats. Int. J. Pharm. 194 (2000) 81-89
-
(2000)
Int. J. Pharm.
, vol.194
, pp. 81-89
-
-
Kim, J.Y.1
Ku, Y.S.2
-
18
-
-
0037027847
-
Pharmakokinetic and pharmacodynamic evaluation of cyclosporin A O/W-emulsion in rats
-
Kim S.-J., Choi H.-K., and Lee Y.-B. Pharmakokinetic and pharmacodynamic evaluation of cyclosporin A O/W-emulsion in rats. Int. J. Pharm. 249 (2002) 149-156
-
(2002)
Int. J. Pharm.
, vol.249
, pp. 149-156
-
-
Kim, S.-J.1
Choi, H.-K.2
Lee, Y.-B.3
-
19
-
-
0035895309
-
Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10: formulation development and bioavailability assessment
-
Kommuru T.R., Gurley B., Khan M.A., and Reddy I.K. 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
-
20
-
-
0001684496
-
The effect of dosage form on oral absorption of L-365260, a potent CCKB receptor antagonist, in beagle dogs
-
Lin J.H., Chen I.W., and Lievens H. The effect of dosage form on oral absorption of L-365260, a potent CCKB receptor antagonist, in beagle dogs. Pharm. Res. 8 (1991) S-272
-
(1991)
Pharm. Res.
, vol.8
-
-
Lin, J.H.1
Chen, I.W.2
Lievens, H.3
-
21
-
-
0028079609
-
Influence of a fat-rich meal on the pharmacokinetics of a new oral formulation of cyclosporine in a crossover comparison with the market formulation
-
Mueller E.A., Kovarik J.M., van Bree J.B., Grevel J., Lucker P.W., and Kutz K. Influence of a fat-rich meal on the pharmacokinetics of a new oral formulation of cyclosporine in a crossover comparison with the market formulation. Pharm. Res. 11 (1994) 151-155
-
(1994)
Pharm. Res.
, vol.11
, pp. 151-155
-
-
Mueller, E.A.1
Kovarik, J.M.2
van Bree, J.B.3
Grevel, J.4
Lucker, P.W.5
Kutz, K.6
-
22
-
-
0021140493
-
The effect of different oils on the absorption of probucol in the rat
-
Palin K.J., and Winson C.G. The effect of different oils on the absorption of probucol in the rat. J. Pharm. Pharmacol. 36 (1984) 641-643
-
(1984)
J. Pharm. Pharmacol.
, vol.36
, pp. 641-643
-
-
Palin, K.J.1
Winson, C.G.2
-
23
-
-
33645016577
-
Accelrated stability testing for prediction of drug product stability
-
Pope D.G. Accelrated stability testing for prediction of drug product stability. Drug Cosmetic Ind. (1980) 48-116
-
(1980)
Drug Cosmetic Ind.
, pp. 48-116
-
-
Pope, D.G.1
-
24
-
-
0343051915
-
Uptake of drugs into the intestinal lymphatics after oral administration
-
Porter C.J., and Charman W.N. Uptake of drugs into the intestinal lymphatics after oral administration. Adv. Drug Deliv. Rev. 25 (1997) 71-89
-
(1997)
Adv. Drug Deliv. Rev.
, vol.25
, pp. 71-89
-
-
Porter, C.J.1
Charman, W.N.2
-
25
-
-
4344578729
-
Susceptibility to lipase-mediated digestion reduces the oral bioavailability of danazol after administration as a medium-chain lipid-based microemulsion formulation
-
Porter C.J., Kaukonen A.M., Boyd B.J., Edwards G.A., and Charman W.N. Susceptibility to lipase-mediated digestion reduces the oral bioavailability of danazol after administration as a medium-chain lipid-based microemulsion formulation. Pharm. Res. 21 (2004) 1405-1412
-
(2004)
Pharm. Res.
, vol.21
, pp. 1405-1412
-
-
Porter, C.J.1
Kaukonen, A.M.2
Boyd, B.J.3
Edwards, G.A.4
Charman, W.N.5
-
26
-
-
0022366625
-
Self-emulsifying drug delivery systems: assessment of the efficiency of emulsification
-
Pouton C.W. Self-emulsifying drug delivery systems: 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
-
27
-
-
0028194817
-
Self-emulsifying drug delivery systems (SEDDS) with polyglycolyzed glycerides for improving in vitro dissolution and oral absorption of lipophilic drugs
-
Shah N.H., Carvajal M.T., Patel C.I., Infeld M.H., and Malick A.W. 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, M.H.4
Malick, A.W.5
-
29
-
-
0024565173
-
Enhanced intestinal absorption of cyclosporine in rats through the reduction of emulsion droplet size
-
Tarr B.D., and Yalkowsky S.H. Enhanced intestinal absorption of cyclosporine in rats through the reduction of emulsion droplet size. Pharm. Res. 6 (1989) 40-43
-
(1989)
Pharm. Res.
, vol.6
, pp. 40-43
-
-
Tarr, B.D.1
Yalkowsky, S.H.2
-
30
-
-
0003045016
-
Evaluation of the self-emulsifying performance of a non-ionic surfactant-vegetable oil mixture
-
Wakerly M.G., Pouton C.W., and Meakin B.J. Evaluation of the self-emulsifying performance of a non-ionic surfactant-vegetable oil mixture. J. Pharm. Pharmacol. 39 (1987) 6P
-
(1987)
J. Pharm. Pharmacol.
, vol.39
-
-
Wakerly, M.G.1
Pouton, C.W.2
Meakin, B.J.3
-
31
-
-
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.N., Lambert G., and 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. 21 (2004) 261-270
-
(2004)
Pharm. Res.
, vol.21
, pp. 261-270
-
-
Yang, S.1
Gursoy, R.N.2
Lambert, G.3
Benita, S.4
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