-
1
-
-
0343527392
-
Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards
-
DOI: 10.1016/S0939-6411(00)00091-6
-
R. Lobenberg and G. L. Amidon, Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards, Eur. J. Pharm. Biopharm. 50 (2000) 3-12; DOI: 10.1016/S0939-6411(00)00091-6.
-
(2000)
Eur. J. Pharm. Biopharm
, vol.50
, pp. 3-12
-
-
Lobenberg, R.1
Amidon, G.L.2
-
2
-
-
85176822415
-
-
H. Yan, S. E. Tabibi and S. H. Yalkowsky, Solubilization of two structurally related anticancer drugs: XK-469 and PPA, J. Pharm. Sci. 95 (2006) 97-107; DOI: 10.1002/jps.20500.
-
H. Yan, S. E. Tabibi and S. H. Yalkowsky, Solubilization of two structurally related anticancer drugs: XK-469 and PPA, J. Pharm. Sci. 95 (2006) 97-107; DOI: 10.1002/jps.20500.
-
-
-
-
3
-
-
1042264121
-
Impact of solid state properties on developability assessment of drug candidates
-
DOI: 10.1016/j.addr.2003.10.007
-
L. F. Huang and W. Q. Tong, Impact of solid state properties on developability assessment of drug candidates, Adv. Drug Del. Rev. 56 (2004) 321-334; DOI: 10.1016/j.addr.2003.10.007.
-
(2004)
Adv. Drug Del. Rev
, vol.56
, pp. 321-334
-
-
Huang, L.F.1
Tong, W.Q.2
-
4
-
-
20344391910
-
Trends in solubility of polymorphs
-
DOI: 10.1002/jps.20302
-
M. Pudipeddi and A. T. M. Serajuddin, Trends in solubility of polymorphs, J. Pharm. Sci. 94 (2005) 929-939; DOI: 10.1002/jps.20302.
-
(2005)
J. Pharm. Sci
, vol.94
, pp. 929-939
-
-
Pudipeddi, M.1
Serajuddin, A.T.M.2
-
5
-
-
0037074108
-
The mechanisms of drug release from solid dispersions in water-soluble polymers
-
DOI: 10.1016/S0378-5173(01)00891-2
-
D. Q. M. Craig, The mechanisms of drug release from solid dispersions in water-soluble polymers, Int. J. Pharm. 231 (2002) 131-144; DOI: 10.1016/S0378-5173(01)00891-2.
-
(2002)
Int. J. Pharm
, vol.231
, pp. 131-144
-
-
Craig, D.Q.M.1
-
6
-
-
34548672900
-
A comparative assessment of solubility advantage from glassy and crystalline forms of a water-insoluble drug
-
DOI: 10.1016/j.ejps.2007.05.111
-
G. Chawla and A. K. Bansal, A comparative assessment of solubility advantage from glassy and crystalline forms of a water-insoluble drug, Eur. J. Pharm. Sci. 32 (2007) 45-57; DOI: 10.1016/j.ejps.2007.05.111.
-
(2007)
Eur. J. Pharm. Sci
, vol.32
, pp. 45-57
-
-
Chawla, G.1
Bansal, A.K.2
-
7
-
-
10844266571
-
Kinetics of decomposition of irbesartan in aqueous solutions determined by high performance liquid chromatography
-
C. J. Mbah, Kinetics of decomposition of irbesartan in aqueous solutions determined by high performance liquid chromatography, Pharmazie 59 (1994) 920-922.
-
(1994)
Pharmazie
, vol.59
, pp. 920-922
-
-
Mbah, C.J.1
-
8
-
-
0036531002
-
Dissolution and phase transition of pharmaceutical compounds
-
DOI: 10.1016/S0022-0248(01)02282-5
-
E. Garcia, C. Hoff and S. Veesler, Dissolution and phase transition of pharmaceutical compounds, J. Crys. Growth 237-239 (2002) 2233-2239; DOI: 10.1016/S0022-0248(01)02282-5.
-
(2002)
J. Crys. Growth
, vol.237-239
, pp. 2233-2239
-
-
Garcia, E.1
Hoff, C.2
Veesler, S.3
-
9
-
-
0347995143
-
Phase transitions in supersaturated drug solution
-
DOI: 10.1021/op034089f
-
S. Veesler, L. Lafferrere, E. Garcia and C. Hoff, Phase transitions in supersaturated drug solution, Org. Process Res. Develop. 7 (2003) 983-989; DOI: 10.1021/op034089f.
-
(2003)
Org. Process Res. Develop
, vol.7
, pp. 983-989
-
-
Veesler, S.1
Lafferrere, L.2
Garcia, E.3
Hoff, C.4
-
10
-
-
0034886795
-
Physicochemical considerations in the preparation of amorphous ritonavir-poly(ethylene glycol) 8000 solid dispersions
-
DOI: 10.1002/jps.1054
-
B. Law, S. L. Krill, E. A. Schmitt, J. J. Fort, Y. Qiu, W. Wang and W. R. Porter, Physicochemical considerations in the preparation of amorphous ritonavir-poly(ethylene glycol) 8000 solid dispersions, J. Pharm. Sci. 90 (2001) 1015-1025; DOI: 10.1002/jps.1054.
-
(2001)
J. Pharm. Sci
, vol.90
, pp. 1015-1025
-
-
Law, B.1
Krill, S.L.2
Schmitt, E.A.3
Fort, J.J.4
Qiu, Y.5
Wang, W.6
Porter, W.R.7
-
11
-
-
33747033371
-
Development, characterization and stabilization of amorphous form of a low Tg drug
-
DOI: 10.1016/j.powtec.2006.05.012
-
V. B. Pokharkar, L. P. Mandpe, M. N. Padamwar, A. A. Ambike, K. R. Mahadik and A. Paradkar, Development, characterization and stabilization of amorphous form of a low Tg drug, Powder Technol. 167 (2006) 20-25; DOI: 10.1016/j.powtec.2006.05.012.
-
(2006)
Powder Technol
, vol.167
, pp. 20-25
-
-
Pokharkar, V.B.1
Mandpe, L.P.2
Padamwar, M.N.3
Ambike, A.A.4
Mahadik, K.R.5
Paradkar, A.6
-
12
-
-
0015124656
-
Pharmaceutical applications of solid dispersion systems
-
DOI: 10.1002/jps.2600600902
-
W. L. Chiou and S. Riegelman, Pharmaceutical applications of solid dispersion systems, J. Pharm. Sci. 60 (1971) 1281-1302; DOI: 10.1002/jps.2600600902.
-
(1971)
J. Pharm. Sci
, vol.60
, pp. 1281-1302
-
-
Chiou, W.L.1
Riegelman, S.2
-
13
-
-
0031393654
-
Preparation and dissolution behavior of ethenzamide solid dispersions using various sugars as dispersion carriers
-
K. Danjo, T. Nakata and A. Otsuka, Preparation and dissolution behavior of ethenzamide solid dispersions using various sugars as dispersion carriers, Chem. Pharm. Bull. 45 (1997) 1840-1844.
-
(1997)
Chem. Pharm. Bull
, vol.45
, pp. 1840-1844
-
-
Danjo, K.1
Nakata, T.2
Otsuka, A.3
-
14
-
-
0035095847
-
Characterization of glass solutions of poorly water-soluble drugs produced by melt extrusion with hydrophilic amorphous polymers
-
DOI: 10.1211/0022357011775532
-
A. Forster, J. Hempenstall and T. Rades, Characterization of glass solutions of poorly water-soluble drugs produced by melt extrusion with hydrophilic amorphous polymers, J. Pharm. Pharmacol. 53 (2001) 303-315; DOI: 10.1211/0022357011775532.
-
(2001)
J. Pharm. Pharmacol
, vol.53
, pp. 303-315
-
-
Forster, A.1
Hempenstall, J.2
Rades, T.3
-
15
-
-
33748209143
-
Enhancement of dissolution profile by solid dispersion (kneading) technique
-
DOI: 10.1208/pt070368
-
A. Modi and P. Tayade, Enhancement of dissolution profile by solid dispersion (kneading) technique, AAPS PharmSciTech. 7 (2006) E1-E6; DOI: 10.1208/pt070368.
-
(2006)
AAPS PharmSciTech
, vol.7
-
-
Modi, A.1
Tayade, P.2
-
16
-
-
33746630521
-
Physicochemical characterization of meloxicam-mannitol binary systems
-
DOI: 10.1016/j.jpba.2006.02.055
-
P. R. Nassab, R. Rajko and P. S. Revesz, Physicochemical characterization of meloxicam-mannitol binary systems, J. Pharm. Biomed. Anal. 41 (2006) 1191-1197; DOI: 10.1016/j.jpba.2006.02.055.
-
(2006)
J. Pharm. Biomed. Anal
, vol.41
, pp. 1191-1197
-
-
Nassab, P.R.1
Rajko, R.2
Revesz, P.S.3
-
17
-
-
0041177972
-
Study by DSC and HSM of the oxazepam-PEG 6000 and oxazepam-D-mannitol systems: Application to the preparation of solid dispersions
-
DOI: 10.1016/S0040-6031(98)00437-7
-
M. J. Arias, J. R. Moyano and J. M. Gines, Study by DSC and HSM of the oxazepam-PEG 6000 and oxazepam-D-mannitol systems: Application to the preparation of solid dispersions, Thermochim. Acta 321 (1998) 33-41; DOI: 10.1016/S0040-6031(98)00437-7.
-
(1998)
Thermochim. Acta
, vol.321
, pp. 33-41
-
-
Arias, M.J.1
Moyano, J.R.2
Gines, J.M.3
-
18
-
-
0031845544
-
Thermal analysis as a screening technique in preformulation studies on picotinamide solid dosage forms
-
DOI: 10.3109/03639049809082722
-
P. Mura, M. T. Faucci, A. Manderioli, S. Furlanetto and S. Pinzauti, Thermal analysis as a screening technique in preformulation studies on picotinamide solid dosage forms, Drug Dev. Ind. Pharm. 24 (1998) 747-756; DOI: 10.3109/03639049809082722.
-
(1998)
Drug Dev. Ind. Pharm
, vol.24
, pp. 747-756
-
-
Mura, P.1
Faucci, M.T.2
Manderioli, A.3
Furlanetto, S.4
Pinzauti, S.5
-
19
-
-
0032915277
-
Development of a mathematical model for the water distribution in freeze-dried solids
-
DOI: 10.1023A: 1018812305562
-
H. K. Chan, K. L. Au-Yeung and I. Gonda, Development of a mathematical model for the water distribution in freeze-dried solids, Pharmacol. Res. 16 (1999) 660-665; DOI: 10.1023A: 1018812305562.
-
(1999)
Pharmacol. Res
, vol.16
, pp. 660-665
-
-
Chan, H.K.1
Au-Yeung, K.L.2
Gonda, I.3
-
20
-
-
3242706588
-
Phase behaviour analysis of solid dispersions of loperamide and two structurally related compounds with the polymers PVP-K30 and PVP-VA64
-
DOI: 10.1016/j.ejps.2004. 04.002
-
I. Weuts, D. Kempen, A. Decorte, G. Verreck, J. Peeters, M. Brewster and G. van den Mooter, Phase behaviour analysis of solid dispersions of loperamide and two structurally related compounds with the polymers PVP-K30 and PVP-VA64, Eur. J. Pharm. Sci. 22 (2004) 375-385; DOI: 10.1016/j.ejps.2004. 04.002.
-
(2004)
Eur. J. Pharm. Sci
, vol.22
, pp. 375-385
-
-
Weuts, I.1
Kempen, D.2
Decorte, A.3
Verreck, G.4
Peeters, J.5
Brewster, M.6
van den Mooter, G.7
-
21
-
-
0001106314
-
Ideal copolymers and the second-order transitions of synthetic rubbers 1: Non-crystalline copolymers
-
M. Gordon and J. S. Taylor, Ideal copolymers and the second-order transitions of synthetic rubbers 1: Non-crystalline copolymers, J. Appl. Chem. 2 (1952) 493-498.
-
(1952)
J. Appl. Chem
, vol.2
, pp. 493-498
-
-
Gordon, M.1
Taylor, J.S.2
-
22
-
-
0031958399
-
Comparison of nicotinamide, ethylurea and polyethylene glycol as carriers for nifedipine solid dispersion systems
-
H. Suzuki and H. Sunada, Comparison of nicotinamide, ethylurea and polyethylene glycol as carriers for nifedipine solid dispersion systems, Chem. Pharm. Bull. 46 (1998) 482-487.
-
(1998)
Chem. Pharm. Bull
, vol.46
, pp. 482-487
-
-
Suzuki, H.1
Sunada, H.2
-
23
-
-
0036794236
-
Selection of suitable drug and excipient candidates to prepare glass solutions by melt extrusion for immediate release oral formulations
-
A. Forster, T. Rades and J. Hempenstall, Selection of suitable drug and excipient candidates to prepare glass solutions by melt extrusion for immediate release oral formulations, Pharm. Technol. (Europe) (2002) 27-37.
-
(2002)
Pharm. Technol. (Europe
, pp. 27-37
-
-
Forster, A.1
Rades, T.2
Hempenstall, J.3
-
24
-
-
45849111476
-
Dissolution rates and supersaturation behavior of amorphous repaglinide particles produced by controlled precipitation
-
DOI: 10.1166/jbn.2007.001
-
P. Sinswat, M. E. Matteucci, K. P. Johnston and R. O. Williams III, Dissolution rates and supersaturation behavior of amorphous repaglinide particles produced by controlled precipitation, J. Biomed. Nanotech. 3 (2007) 18-27; DOI: 10.1166/jbn.2007.001.
-
(2007)
J. Biomed. Nanotech
, vol.3
, pp. 18-27
-
-
Sinswat, P.1
Matteucci, M.E.2
Johnston, K.P.3
Williams III, R.O.4
-
25
-
-
0029047420
-
Influence of the preparation method of solid dispersions on their dissolution rate: Study of triamterene-D-mannitol system
-
DOI: 10.1016/0378-5173(95)00026-F
-
M. J. Arias, J. M. Gines, J. R. Moyano, J. I. Perez-Martinez and A. M. Rabasco, Influence of the preparation method of solid dispersions on their dissolution rate: Study of triamterene-D-mannitol system, Int. J. Pharm. 123 (1995) 25-31; DOI: 10.1016/0378-5173(95)00026-F.
-
(1995)
Int. J. Pharm
, vol.123
, pp. 25-31
-
-
Arias, M.J.1
Gines, J.M.2
Moyano, J.R.3
Perez-Martinez, J.I.4
Rabasco, A.M.5
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