-
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., Lennernäs 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
Lennernäs, H.2
Shah, V.P.3
Crison, J.R.4
-
2
-
-
0002990226
-
Sodium luaryl sulfate
-
Wade A., and Weller P.J. (Eds), Alden Multimedia, Northamton
-
Behn S. Sodium luaryl sulfate. In: Wade A., and Weller P.J. (Eds). Handbook of Pharmaceutical Excipients. 2nd Ed. (1994), Alden Multimedia, Northamton 448-450
-
(1994)
Handbook of Pharmaceutical Excipients. 2nd Ed.
, pp. 448-450
-
-
Behn, S.1
-
3
-
-
0036182021
-
The use of chemically modified cyclodextrins in the development of formulations for chemical delivery systems
-
Brewster M.E., and Loftsson T. The use of chemically modified cyclodextrins in the development of formulations for chemical delivery systems. Pharmazie 57 (2002) 94-101
-
(2002)
Pharmazie
, vol.57
, pp. 94-101
-
-
Brewster, M.E.1
Loftsson, T.2
-
4
-
-
0035998944
-
Effect of mechanical processing on phase composition
-
Brittain H.G. Effect of mechanical processing on phase composition. J. Pharm. Sci. 91 (2002) 1573-1580
-
(2002)
J. Pharm. Sci.
, vol.91
, pp. 1573-1580
-
-
Brittain, H.G.1
-
5
-
-
0037074108
-
The mechanisms of drug release from solid dispersions in water-soluble polymers
-
Craig D.Q.M. The mechanisms of drug release from solid dispersions in water-soluble polymers. Int. J. Pharm. 231 (2002) 131-144
-
(2002)
Int. J. Pharm.
, vol.231
, pp. 131-144
-
-
Craig, D.Q.M.1
-
6
-
-
0346671290
-
Water-soluble prodrugs of dipeptide HIV protease inhibitors based on O → N intramolecular acyl migration: design, synthesis and kinetic study
-
Hamada Y., Matsumoto H., Yamaguchi S., Kimura T., Hayashi Y., and Kiso Y. Water-soluble prodrugs of dipeptide HIV protease inhibitors based on O → N intramolecular acyl migration: design, synthesis and kinetic study. Bioorg. Med. Chem. 12 (2004) 159-170
-
(2004)
Bioorg. Med. Chem.
, vol.12
, pp. 159-170
-
-
Hamada, Y.1
Matsumoto, H.2
Yamaguchi, S.3
Kimura, T.4
Hayashi, Y.5
Kiso, Y.6
-
7
-
-
0032533877
-
Aspect of mechanical activation in terms of comminution theory
-
Juhász Z. Aspect of mechanical activation in terms of comminution theory. Colloids Surf. A: Physicochem. Eng. Aspects 141 (1998) 449-462
-
(1998)
Colloids Surf. A: Physicochem. Eng. Aspects
, vol.141
, pp. 449-462
-
-
Juhász, Z.1
-
8
-
-
0033958846
-
Stability characterization of controlled release coprecipitates and solid dispersions
-
Khan M.A., Karnachi A.A., Agarwal V., Vaithiyalingam S.R., Nazzal S., and Reddy I.K. Stability characterization of controlled release coprecipitates and solid dispersions. J. Control. Release 63 (2000) 1-6
-
(2000)
J. Control. Release
, vol.63
, pp. 1-6
-
-
Khan, M.A.1
Karnachi, A.A.2
Agarwal, V.3
Vaithiyalingam, S.R.4
Nazzal, S.5
Reddy, I.K.6
-
9
-
-
0034601240
-
Improving drug solubility for oral delivery using solid dispersions
-
Leuner C., and Dressman J. Improving drug solubility for oral delivery using solid dispersions. Eur. J. Pharm. Biopharm. 50 (2000) 47-60
-
(2000)
Eur. J. Pharm. Biopharm.
, vol.50
, pp. 47-60
-
-
Leuner, C.1
Dressman, J.2
-
10
-
-
16644373945
-
Design, synthesis and in vitro evaluation of novel water-soluble prodrugs of buparvaquone
-
Mántylá A., Rautio J., Nevalainen T., Keski-Rahkonen P., Vepsälainen J., and Järvinen T. Design, synthesis and in vitro evaluation of novel water-soluble prodrugs of buparvaquone. Eur. J. Pharm. Sci. 23 (2004) 151-158
-
(2004)
Eur. J. Pharm. Sci.
, vol.23
, pp. 151-158
-
-
Mántylá, A.1
Rautio, J.2
Nevalainen, T.3
Keski-Rahkonen, P.4
Vepsälainen, J.5
Järvinen, T.6
-
12
-
-
33644538321
-
Drug nanoparticle formation from drug/HPMC/SDS ternary ground mixture
-
Moribe K., Pongpeerapat A., Tozuka Y., and Yamamoto K. Drug nanoparticle formation from drug/HPMC/SDS ternary ground mixture. Pharmazie 61 (2006) 97-101
-
(2006)
Pharmazie
, vol.61
, pp. 97-101
-
-
Moribe, K.1
Pongpeerapat, A.2
Tozuka, Y.3
Yamamoto, K.4
-
13
-
-
0037026338
-
Investigation of effects of grinding and co-grinding on physicochemical properties of glisentide
-
Mura P., Cirri M., Faucci M.T., Ginès-Dorado J.M., and Bettinetti G.P. Investigation of effects of grinding and co-grinding on physicochemical properties of glisentide. J. Pharm. Biomed. Anal. 30 (2002) 227-237
-
(2002)
J. Pharm. Biomed. Anal.
, vol.30
, pp. 227-237
-
-
Mura, P.1
Cirri, M.2
Faucci, M.T.3
Ginès-Dorado, J.M.4
Bettinetti, G.P.5
-
14
-
-
11144235831
-
Assessment of the combined approach of N-alkylation and salt formation to enhance aqueous solubility of tertiary amines using bupivacaine as a model drug
-
Nielsen A.B., Frydenvang K., Liljefors T., Buur A., and Larsen C. Assessment of the combined approach of N-alkylation and salt formation to enhance aqueous solubility of tertiary amines using bupivacaine as a model drug. Eur. J. Pharm. Sci. 24 (2005) 85-93
-
(2005)
Eur. J. Pharm. Sci.
, vol.24
, pp. 85-93
-
-
Nielsen, A.B.1
Frydenvang, K.2
Liljefors, T.3
Buur, A.4
Larsen, C.5
-
15
-
-
0016075556
-
Milling of pharmaceutical solids
-
Parrott E.L. Milling of pharmaceutical solids. J. Pharm. Sci. 63 (1974) 813-829
-
(1974)
J. Pharm. Sci.
, vol.63
, pp. 813-829
-
-
Parrott, E.L.1
-
16
-
-
33750614933
-
Molecular interaction among Probucol/PVP/SDS multicomponent system investigated by solid-state NMR
-
Pongpeerapat A., Higashi K., Tozuka Y., Moribe K., and Yamamoto K. Molecular interaction among Probucol/PVP/SDS multicomponent system investigated by solid-state NMR. Pharm. Res. 23 (2006) 2566-2574
-
(2006)
Pharm. Res.
, vol.23
, pp. 2566-2574
-
-
Pongpeerapat, A.1
Higashi, K.2
Tozuka, Y.3
Moribe, K.4
Yamamoto, K.5
-
17
-
-
9944247596
-
Formation and stability of nanoparticles obtained from drug/PVP/SDS ternary ground mixture
-
Pongpeerapat A., Itoh K., Tozuka Y., Moribe K., Oguchi T., and Yamamoto K. Formation and stability of nanoparticles obtained from drug/PVP/SDS ternary ground mixture. J. Drug Sci. Tech. 14 (2004) 441-447
-
(2004)
J. Drug Sci. Tech.
, vol.14
, pp. 441-447
-
-
Pongpeerapat, A.1
Itoh, K.2
Tozuka, Y.3
Moribe, K.4
Oguchi, T.5
Yamamoto, K.6
-
18
-
-
39549094916
-
Formation mechanism of colloidal nanoparticles obtained from probucol/PVP/SDS ternary ground mixture
-
Pongpeerapat A., Wanawongthai C., Tozuka Y., Moribe K., and Ymamoto K. Formation mechanism of colloidal nanoparticles obtained from probucol/PVP/SDS ternary ground mixture. Int. J. Pharm. 352 (2008) 309-316
-
(2008)
Int. J. Pharm.
, vol.352
, pp. 309-316
-
-
Pongpeerapat, A.1
Wanawongthai, C.2
Tozuka, Y.3
Moribe, K.4
Ymamoto, K.5
-
20
-
-
38849159854
-
In vivo assessment of oral administration of probucol nanoparticles in rats
-
Shudo J., Pongpeerapat A., Wanawongthai C., Moribe K., and Yamamoto K. In vivo assessment of oral administration of probucol nanoparticles in rats. Biol. Pharm. Bull. 31 (2008) 321-325
-
(2008)
Biol. Pharm. Bull.
, vol.31
, pp. 321-325
-
-
Shudo, J.1
Pongpeerapat, A.2
Wanawongthai, C.3
Moribe, K.4
Yamamoto, K.5
-
21
-
-
0035186701
-
A nifedipine coground mixture with sodium deoxycholate. II. Dissolution characteristics and stability
-
Suzuki H., Ogawa M., Hironaka K., Ito K., and Sunada H. A nifedipine coground mixture with sodium deoxycholate. II. Dissolution characteristics and stability. Drug Dev. Ind. Pharm. 27 (2001) 951-958
-
(2001)
Drug Dev. Ind. Pharm.
, vol.27
, pp. 951-958
-
-
Suzuki, H.1
Ogawa, M.2
Hironaka, K.3
Ito, K.4
Sunada, H.5
-
22
-
-
33746661551
-
Influence of the alkyl tail length on the anionic surfactant-PVP interaction
-
Tadeschi A.M., Busi E., Basodi R., Paduano L., and D'Errico G. Influence of the alkyl tail length on the anionic surfactant-PVP interaction. J. Solut. Chem. 35 (2006) 951-968
-
(2006)
J. Solut. Chem.
, vol.35
, pp. 951-968
-
-
Tadeschi, A.M.1
Busi, E.2
Basodi, R.3
Paduano, L.4
D'Errico, G.5
-
23
-
-
33846176619
-
A provisional biopharmaceutical classification of the top 200 oral drug products in the United States, Great Britain, Spain, and Japan
-
Takagi T., Ramachandran C., Bermejo M., Yamashita S., Yu L.X., and Amidon G.L. A provisional biopharmaceutical classification of the top 200 oral drug products in the United States, Great Britain, Spain, and Japan. Mol. Pharm. 3 (2006) 31-643
-
(2006)
Mol. Pharm.
, vol.3
, pp. 31-643
-
-
Takagi, T.1
Ramachandran, C.2
Bermejo, M.3
Yamashita, S.4
Yu, L.X.5
Amidon, G.L.6
-
24
-
-
16344364096
-
Design and evaluation of cyclodextrin-based drug formulation
-
Uekama K. Design and evaluation of cyclodextrin-based drug formulation. Chem. Pharm. Bull. 52 (2004) 900-915
-
(2004)
Chem. Pharm. Bull.
, vol.52
, pp. 900-915
-
-
Uekama, K.1
-
25
-
-
1842611878
-
Physicochemical characterization of solid dispersions of indomethacin with PEG, 6000 Myrj 52, lactose, sorbitol, dextrin, and Eudragit E100
-
Valizadeh H., Nokhodchi A., Qarakhani N., Zakeri-Milani P., Azarmi S., Hassanzadeh D., and Lobenberg R. Physicochemical characterization of solid dispersions of indomethacin with PEG, 6000 Myrj 52, lactose, sorbitol, dextrin, and Eudragit E100. Drug Dev. Ind. Pharm. 30 (2004) 303-317
-
(2004)
Drug Dev. Ind. Pharm.
, vol.30
, pp. 303-317
-
-
Valizadeh, H.1
Nokhodchi, A.2
Qarakhani, N.3
Zakeri-Milani, P.4
Azarmi, S.5
Hassanzadeh, D.6
Lobenberg, R.7
-
26
-
-
0037142222
-
In vivo evaluation of matrix pellets containing nanocrystalline ketoprofen
-
Vergote G.J., Vervaet C., Driessche I.V., Hoste S., Smedt S.D., Demeester J., Jain R.A., Ruddy S., and Remon J.P. In vivo evaluation of matrix pellets containing nanocrystalline ketoprofen. Int. J. Pharm. 240 (2002) 79-84
-
(2002)
Int. J. Pharm.
, vol.240
, pp. 79-84
-
-
Vergote, G.J.1
Vervaet, C.2
Driessche, I.V.3
Hoste, S.4
Smedt, S.D.5
Demeester, J.6
Jain, R.A.7
Ruddy, S.8
Remon, J.P.9
-
27
-
-
0005108843
-
Povidone
-
Wade A., and Weller P.J. (Eds), Alden Multimedia, Northamton
-
Walking W.D. Povidone. In: Wade A., and Weller P.J. (Eds). Handbook of Pharmaceutical Excipients. 2nd Ed. (1994), Alden Multimedia, Northamton 392-399
-
(1994)
Handbook of Pharmaceutical Excipients. 2nd Ed.
, pp. 392-399
-
-
Walking, W.D.1
-
28
-
-
0030062860
-
Dissolution behavior of probucol from solid dispersion systems of probucol-polyvinylpyrrolidone
-
Yagi N., Terashima Y., Kenmotsu H., Sekikawa H., and Takada M. Dissolution behavior of probucol from solid dispersion systems of probucol-polyvinylpyrrolidone. Chem. Pharm. Bull. 44 (1996) 241-244
-
(1996)
Chem. Pharm. Bull.
, vol.44
, pp. 241-244
-
-
Yagi, N.1
Terashima, Y.2
Kenmotsu, H.3
Sekikawa, H.4
Takada, M.5
-
29
-
-
67349257306
-
Pharmacokinetics of probucol dosage forms in clinical tests
-
Zaitseva T.M., Lupanov V.P., Lyakishev A.A., Titov V.N., and Polevaya T.Y. Pharmacokinetics of probucol dosage forms in clinical tests. Pharm. Chem. J. 29 (1995) 245-247
-
(1995)
Pharm. Chem. J.
, vol.29
, pp. 245-247
-
-
Zaitseva, T.M.1
Lupanov, V.P.2
Lyakishev, A.A.3
Titov, V.N.4
Polevaya, T.Y.5
-
30
-
-
3042757199
-
Synthesis and cytotoxicity of water soluble quaternary salt derivatives of camptothecin
-
Zu Y.G., Li Q.Y., Fu Y.J., and Wang W. Synthesis and cytotoxicity of water soluble quaternary salt derivatives of camptothecin. Bioorg. Med. Chem. Lett. 14 (2004) 4023-4026
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 4023-4026
-
-
Zu, Y.G.1
Li, Q.Y.2
Fu, Y.J.3
Wang, W.4
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