-
1
-
-
0036742053
-
Poorly aqueous solubility: an industry wide problem in drug discovery
-
Lipinski C. Poorly aqueous solubility: an industry wide problem in drug discovery. Am. Pharm. Rev. 5 (2002) 82-85
-
(2002)
Am. Pharm. Rev.
, vol.5
, pp. 82-85
-
-
Lipinski, C.1
-
2
-
-
0035289779
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
Lipinski C.A., Lombardo F., Dominy B.W., and Feeney P.J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Deliv. Rev. 46 (2001) 3-26
-
(2001)
Adv. Drug Deliv. Rev.
, vol.46
, pp. 3-26
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
3
-
-
0034461768
-
Drug-like properties and the causes of poor solubility and poor permeability
-
Lipinski C.A. Drug-like properties and the causes of poor solubility and poor permeability. J. Pharmacol. Toxicol. Methods 44 (2000) 235-249
-
(2000)
J. Pharmacol. Toxicol. Methods
, vol.44
, pp. 235-249
-
-
Lipinski, C.A.1
-
4
-
-
34547864243
-
Drug delivery strategies for poorly water-soluble drugs
-
Fahr A., and Liu X. Drug delivery strategies for poorly water-soluble drugs. Expert Opin. Drug Deliv. 4 (2007) 403-416
-
(2007)
Expert Opin. Drug Deliv.
, vol.4
, pp. 403-416
-
-
Fahr, A.1
Liu, X.2
-
5
-
-
0032885450
-
Solid dispersions of poorly water-soluble drugs: early promises, subsequent problems, and recent breakthroughs
-
Serajuddin A.T.M. Solid dispersions of poorly water-soluble drugs: early promises, subsequent problems, and recent breakthroughs. J. Pharm. Sci. 88 (1999) 1058-1066
-
(1999)
J. Pharm. Sci.
, vol.88
, pp. 1058-1066
-
-
Serajuddin, A.T.M.1
-
6
-
-
0027243792
-
Improved oral absorption of a poorly water-soluble drug, HO-221, by wet-bead milling producing particles in submicron region
-
Kondo N., Iwao T., Masuda H., Yamanouchi K., Ishihara Y., Yamada N., Haga T., Ogawa Y., and Yokoyama K. Improved oral absorption of a poorly water-soluble drug, HO-221, by wet-bead milling producing particles in submicron region. Chem. Pharm. Bull. (Tokyo) 41 (1993) 737-740
-
(1993)
Chem. Pharm. Bull. (Tokyo)
, vol.41
, pp. 737-740
-
-
Kondo, N.1
Iwao, T.2
Masuda, H.3
Yamanouchi, K.4
Ishihara, Y.5
Yamada, N.6
Haga, T.7
Ogawa, Y.8
Yokoyama, K.9
-
7
-
-
0029080002
-
Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: I. Absolute oral bioavailability of nanocrystalline danazol in beagle dogs
-
Liversidge G.G., and Cundy K.C. Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: I. Absolute oral bioavailability of nanocrystalline danazol in beagle dogs. Int. J. Pharm. 125 (1995) 91-97
-
(1995)
Int. J. Pharm.
, vol.125
, pp. 91-97
-
-
Liversidge, G.G.1
Cundy, K.C.2
-
9
-
-
20844446627
-
The role of biopharmaceutics in the development of a clinical nanoparticle formulation of MK-0869: a Beagle dog model predicts improved bioavailability and diminished food effect on absorption in human
-
Wu Y., Loper A., Landis E., Hettrick L., Novak L., Lynn K., Chen C., Thompson K., Higgins R., Batra U., Shelukar S., Kwei G., and Storey D. The role of biopharmaceutics in the development of a clinical nanoparticle formulation of MK-0869: a Beagle dog model predicts improved bioavailability and diminished food effect on absorption in human. Int. J. Pharm. 285 (2004) 135-146
-
(2004)
Int. J. Pharm.
, vol.285
, pp. 135-146
-
-
Wu, Y.1
Loper, A.2
Landis, E.3
Hettrick, L.4
Novak, L.5
Lynn, K.6
Chen, C.7
Thompson, K.8
Higgins, R.9
Batra, U.10
Shelukar, S.11
Kwei, G.12
Storey, D.13
-
10
-
-
32544458008
-
Absence of food effect with a 145 mg nanoparticle fenofibrate tablet formulation
-
Sauron R., Wilkins M., Jessent V., Dubois A., Maillot C., and Weil A. Absence of food effect with a 145 mg nanoparticle fenofibrate tablet formulation. Int. J. Clin. Pharm. Ther. 44 (2006) 64-70
-
(2006)
Int. J. Clin. Pharm. Ther.
, vol.44
, pp. 64-70
-
-
Sauron, R.1
Wilkins, M.2
Jessent, V.3
Dubois, A.4
Maillot, C.5
Weil, A.6
-
11
-
-
33344478634
-
Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs
-
Jinno J., Kamada N., Miyake M., Yamada K., Mukai T., Odomi M., Toguchi H., Liversidge G.G., Higaki K., and Kimura T. Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs. J. Control. Release 111 (2006) 56-64
-
(2006)
J. Control. Release
, vol.111
, pp. 56-64
-
-
Jinno, J.1
Kamada, N.2
Miyake, M.3
Yamada, K.4
Mukai, T.5
Odomi, M.6
Toguchi, H.7
Liversidge, G.G.8
Higaki, K.9
Kimura, T.10
-
12
-
-
1842559836
-
Nanoparticle engineering processes for enhancing the dissolution rates of poorly water soluble drugs
-
Hu J., Johnston K.P., and Williams III R.O. Nanoparticle engineering processes for enhancing the dissolution rates of poorly water soluble drugs. Drug Dev. Ind. Pharm. 30 (2004) 233-245
-
(2004)
Drug Dev. Ind. Pharm.
, vol.30
, pp. 233-245
-
-
Hu, J.1
Johnston, K.P.2
Williams III, R.O.3
-
13
-
-
28444461830
-
Drug nanocrystals of poorly soluble drugs produced by high pressure homogenisation
-
Keck C.M., and Muller R.H. Drug nanocrystals of poorly soluble drugs produced by high pressure homogenisation. Eur. J. Pharm. Biopharm. 62 (2006) 3-16
-
(2006)
Eur. J. Pharm. Biopharm.
, vol.62
, pp. 3-16
-
-
Keck, C.M.1
Muller, R.H.2
-
14
-
-
0038032150
-
Solid lipid nanoparticles (SLN) for controlled drug delivery - a review of the state of the art
-
Muller R.H., Mader K., and Gohla S. Solid lipid nanoparticles (SLN) for controlled drug delivery - a review of the state of the art. Eur. J. Pharm. Biopharm. 50 (2000) 161-177
-
(2000)
Eur. J. Pharm. Biopharm.
, vol.50
, pp. 161-177
-
-
Muller, R.H.1
Mader, K.2
Gohla, S.3
-
15
-
-
0343487750
-
Formulation of self-emulsifying drug delivery systems
-
Pouton C.W. 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
-
16
-
-
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
-
17
-
-
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
-
18
-
-
34547861305
-
Nanosizing of a drug/carrageenan complex to increase solubility and dissolution rate
-
Dai W., Dong L.C., and Song Y. Nanosizing of a drug/carrageenan complex to increase solubility and dissolution rate. Int. J. Pharm. 342 (2007) 201-207
-
(2007)
Int. J. Pharm.
, vol.342
, pp. 201-207
-
-
Dai, W.1
Dong, L.C.2
Song, Y.3
-
19
-
-
33846783997
-
Turbidimetric measurement and prediction of dissolution rates of poorly soluble drug nanocrystals
-
Crisp M.T., Tucker C.J., Rogers T.L., Williams III R.O., and Johnston K.P. Turbidimetric measurement and prediction of dissolution rates of poorly soluble drug nanocrystals. J. Control. Release 117 (2007) 351-359
-
(2007)
J. Control. Release
, vol.117
, pp. 351-359
-
-
Crisp, M.T.1
Tucker, C.J.2
Rogers, T.L.3
Williams III, R.O.4
Johnston, K.P.5
-
21
-
-
0242290406
-
Limited influence of P-glycoprotein on small-intestinal absorption of cilostazol, a high absorptive permeability drug
-
Toyobuku H., Tamai I., Ueno K., and Tsuji A. Limited influence of P-glycoprotein on small-intestinal absorption of cilostazol, a high absorptive permeability drug. J. Pharm. Sci. 92 (2003) 2249-2259
-
(2003)
J. Pharm. Sci.
, vol.92
, pp. 2249-2259
-
-
Toyobuku, H.1
Tamai, I.2
Ueno, K.3
Tsuji, A.4
-
22
-
-
0024596954
-
The effect of particle size distribution on dissolution rate and oral absorption
-
Hints R.J., and Johnson K.C. The effect of particle size distribution on dissolution rate and oral absorption. Int. J. Pharm. 51 (1989) 9-17
-
(1989)
Int. J. Pharm.
, vol.51
, pp. 9-17
-
-
Hints, R.J.1
Johnson, K.C.2
-
23
-
-
0141680647
-
Dissolution and absorption modeling: model expansion to simulate the effects of precipitation, water absorption, longitudinally changing intestinal permeability, and controlled release on drug absorption
-
Johnson K.C. Dissolution and absorption modeling: model expansion to simulate the effects of precipitation, water absorption, longitudinally changing intestinal permeability, and controlled release on drug absorption. Drug Dev. Ind. Pharm. 29 (2003) 833-842
-
(2003)
Drug Dev. Ind. Pharm.
, vol.29
, pp. 833-842
-
-
Johnson, K.C.1
-
24
-
-
0033496577
-
Relative bioavailability and effects of a high fat meal on single dose cilostazol pharmacokinetics
-
Bramer S.L., and Forbes W.P. Relative bioavailability and effects of a high fat meal on single dose cilostazol pharmacokinetics. Clin. Pharmacokinet. 37 Suppl 2 (1999) 13-23
-
(1999)
Clin. Pharmacokinet.
, vol.37
, Issue.SUPPL. 2
, pp. 13-23
-
-
Bramer, S.L.1
Forbes, W.P.2
-
25
-
-
21844461846
-
Preparation and characterization of nanocrystals for solubility and dissolution rate enhancement of nifedipine
-
Hecq J., Deleers M., Fanara D., Vranckx H., and Amighi K. Preparation and characterization of nanocrystals for solubility and dissolution rate enhancement of nifedipine. Int. J. Pharm. 299 (2005) 167-177
-
(2005)
Int. J. Pharm.
, vol.299
, pp. 167-177
-
-
Hecq, J.1
Deleers, M.2
Fanara, D.3
Vranckx, H.4
Amighi, K.5
-
26
-
-
0031913402
-
Dissolution testing as a prognostic tool for oral drug absorption: immediate release dosage forms
-
Dressman J.B., Amidon G.L., Reppas C., and Shah V.P. Dissolution testing as a prognostic tool for oral drug absorption: immediate release dosage forms. Pharm. Res. 15 (1998) 11-22
-
(1998)
Pharm. Res.
, vol.15
, pp. 11-22
-
-
Dressman, J.B.1
Amidon, G.L.2
Reppas, C.3
Shah, V.P.4
-
28
-
-
0036481691
-
Gastrointestinal transit and drug absorption
-
Kimura T., and Higaki K. Gastrointestinal transit and drug absorption. Biol. Pharm. Bull. 25 (2002) 149-164
-
(2002)
Biol. Pharm. Bull.
, vol.25
, pp. 149-164
-
-
Kimura, T.1
Higaki, K.2
-
29
-
-
34248582287
-
Prediction of oral absorption of griseofulvin, BCS class II drug, based on GITA model: utilization of a more suitable medium for in vitro dissolution study
-
Fujioka Y., Kadono K., Fujie Y., Metsugi Y., Ogawara K., Higaki K., and Kimura T. Prediction of oral absorption of griseofulvin, BCS class II drug, based on GITA model: utilization of a more suitable medium for in vitro dissolution study. J. Control. Release 119 (2007) 222-228
-
(2007)
J. Control. Release
, vol.119
, pp. 222-228
-
-
Fujioka, Y.1
Kadono, K.2
Fujie, Y.3
Metsugi, Y.4
Ogawara, K.5
Higaki, K.6
Kimura, T.7
-
30
-
-
39449086202
-
Evaluation of in vivo dissolution behavior and GI transit of griseofulvin, a BCS class II drug
-
Fujioka Y., Metsugi Y., Ogawara K., Higaki K., and Kimura T. Evaluation of in vivo dissolution behavior and GI transit of griseofulvin, a BCS class II drug. Int. J. Pharm. 352 (2008) 36-43
-
(2008)
Int. J. Pharm.
, vol.352
, pp. 36-43
-
-
Fujioka, Y.1
Metsugi, Y.2
Ogawara, K.3
Higaki, K.4
Kimura, T.5
-
31
-
-
84874877344
-
-
Wade A., and Weller P.J. (Eds), The Pharmaceutical Press, London
-
In: Wade A., and Weller P.J. (Eds). Handbook of Pharmaceutical Excipients. 2nd Ed. (1994), The Pharmaceutical Press, London 448-450
-
(1994)
Handbook of Pharmaceutical Excipients. 2nd Ed.
, pp. 448-450
-
-
-
32
-
-
0026101530
-
Physicochemical aspects of drug release. XIII. The effect of sodium dodecyl sulfate additions on the structure and dissolution of a drug in solid dispersions
-
Sjokvist E., Nystrom C., and Alden M. Physicochemical aspects of drug release. XIII. The effect of sodium dodecyl sulfate additions on the structure and dissolution of a drug in solid dispersions. Int. J. Pharm. 69 (1991) 53-62
-
(1991)
Int. J. Pharm.
, vol.69
, pp. 53-62
-
-
Sjokvist, E.1
Nystrom, C.2
Alden, M.3
-
33
-
-
0025930844
-
Solubilization and wetting effects of bile salts on the dissolution of steroids
-
Bakatselou V., Oppenheim R.C., and Dressman J.B. Solubilization and wetting effects of bile salts on the dissolution of steroids. Pharm. Res. 8 (1991) 1461-1469
-
(1991)
Pharm. Res.
, vol.8
, pp. 1461-1469
-
-
Bakatselou, V.1
Oppenheim, R.C.2
Dressman, J.B.3
-
34
-
-
0035660775
-
Evaluation and selection of bio-relevant dissolution media for a poorly water-soluble new chemical entity
-
Tang L., Khan S.U., and Muhammad N.A. Evaluation and selection of bio-relevant dissolution media for a poorly water-soluble new chemical entity. Pharm. Dev. Technol. 6 (2001) 531-540
-
(2001)
Pharm. Dev. Technol.
, vol.6
, pp. 531-540
-
-
Tang, L.1
Khan, S.U.2
Muhammad, N.A.3
-
35
-
-
0026502791
-
Physicochemical aspects of drug release. XIV. The effects of some ionic and non-ionic surfactants on properties of a sparingly soluble drug in solid dispersions
-
Sjokvist E., Nystrom C., Alden M., and Caram-Lelham N. Physicochemical aspects of drug release. XIV. The effects of some ionic and non-ionic surfactants on properties of a sparingly soluble drug in solid dispersions. Int. J. Pharm. 79 (1992) 123-133
-
(1992)
Int. J. Pharm.
, vol.79
, pp. 123-133
-
-
Sjokvist, E.1
Nystrom, C.2
Alden, M.3
Caram-Lelham, N.4
-
36
-
-
0028848465
-
The wetting of powders by bile salt solutions and gastric juice
-
Fell J.T., and Mohammad H.A.H. The wetting of powders by bile salt solutions and gastric juice. Int. J. Pharm. 125 (1995) 327-330
-
(1995)
Int. J. Pharm.
, vol.125
, pp. 327-330
-
-
Fell, J.T.1
Mohammad, H.A.H.2
-
37
-
-
32244434196
-
Characterization of the human upper gastrointestinal contents under conditions simulating bioavailability/bioequivalence studies
-
Kalantzi L., Goumas K., Kalioras V., Abrahamsson B., Dressman J.B., and Reppas C. Characterization of the human upper gastrointestinal contents under conditions simulating bioavailability/bioequivalence studies. Pharm. Res. 23 (2006) 165-176
-
(2006)
Pharm. Res.
, vol.23
, pp. 165-176
-
-
Kalantzi, L.1
Goumas, K.2
Kalioras, V.3
Abrahamsson, B.4
Dressman, J.B.5
Reppas, C.6
-
38
-
-
33745377516
-
Canine intestinal contents vs. simulated media for the assessment of solubility of two weak bases in the human small intestinal contents
-
Kalantzi L., Persson E., Polentarutti B., Abrahamsson B., Goumas K., Dressman J.B., and Reppas C. Canine intestinal contents vs. simulated media for the assessment of solubility of two weak bases in the human small intestinal contents. Pharm. Res. 23 (2006) 1373-1381
-
(2006)
Pharm. Res.
, vol.23
, pp. 1373-1381
-
-
Kalantzi, L.1
Persson, E.2
Polentarutti, B.3
Abrahamsson, B.4
Goumas, K.5
Dressman, J.B.6
Reppas, C.7
-
39
-
-
14144250013
-
In vivo in vitro correlations for a poorly soluble drug, danazol, using the flow-through dissolution method with biorelevant dissolution media
-
Sunesen V.H., Pedersen B.L., Kristensen H.G., and Mullertz A. In vivo in vitro correlations for a poorly soluble drug, danazol, using the flow-through dissolution method with biorelevant dissolution media. Eur. J. Pharm. Sci. 24 (2005) 305-313
-
(2005)
Eur. J. Pharm. Sci.
, vol.24
, pp. 305-313
-
-
Sunesen, V.H.1
Pedersen, B.L.2
Kristensen, H.G.3
Mullertz, A.4
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