-
1
-
-
0002820601
-
Poorly soluble drugs, a challenge in drug delivery
-
Muller RH, Benita S, Bohm B Eds, Medpharm Scientific Publishers, Stuttgart
-
Speiser P .P., Poorly soluble drugs, a challenge in drug delivery. In: Muller RH, Benita S, Bohm B Eds Emulsions and nanosuspensions for the formulation of poorly soluble drugs, Medpharm Scientific Publishers, Stuttgart, 1998, 15-28.
-
(1998)
Emulsions and nanosuspensions for the formulation of poorly soluble drugs
, pp. 15-28
-
-
Speiser, P.P.1
-
2
-
-
77953471412
-
-
Chaudhari P. D., Sharma P. K., Badagale M. M., Dave K. D., Kulkarni P. A., Barhate N. S., Current trends in solid dispersions technology, Pharmainfotech, 2006.
-
Chaudhari P. D., Sharma P. K., Badagale M. M., Dave K. D., Kulkarni P. A., Barhate N. S., Current trends in solid dispersions technology, Pharmainfotech, 2006.
-
-
-
-
3
-
-
77953470828
-
-
th edition Merck Research Laboratory, 2001.
-
th edition Merck Research Laboratory, 2001.
-
-
-
-
5
-
-
33744909400
-
-
Article
-
Viswanathan C. L., Kulkarni S. K., Kolwankar D. R., Spherical Agglomeration of Mefenamic Acid and Nabumetone to Improve Micromeritics and Solubility: A Technical Note, AAPS PharmSciTech., 2006, 7(2), Article 48.
-
(2006)
Spherical Agglomeration of Mefenamic Acid and Nabumetone to Improve Micromeritics and Solubility: A Technical Note, AAPS PharmSciTech
, vol.7
, Issue.2
, pp. 48
-
-
Viswanathan, C.L.1
Kulkarni, S.K.2
Kolwankar, D.R.3
-
6
-
-
0037189994
-
-
Sarkari M., Brown J., Chen X., Swinnea S., Williams R. O., Johnston K. P., Enhancement drug dissolution using evaporative precipitation into aqueous solution, Int. J. Pharm., 2002, 28;243(1-2), 17-31.
-
Sarkari M., Brown J., Chen X., Swinnea S., Williams R. O., Johnston K. P., Enhancement drug dissolution using evaporative precipitation into aqueous solution, Int. J. Pharm., 2002, 28;243(1-2), 17-31.
-
-
-
-
7
-
-
0037467170
-
Microcrystals for dissolution rate enhancement of poorly water-soluble drugs
-
Rasenack N., Hartenhauer H., Müller B.W., Microcrystals for dissolution rate enhancement of poorly water-soluble drugs, International Journal of Pharmaceutics, 254 (2): 137-145.
-
International Journal of Pharmaceutics
, vol.254
, Issue.2
, pp. 137-145
-
-
Rasenack, N.1
Hartenhauer, H.2
Müller, B.W.3
-
8
-
-
0035859996
-
Stabilization of supersaturated solutions of a lipophilic drug for dermal delivery
-
Moser K., Kriwet K., Kalia Y. N., Guy R. H., Stabilization of supersaturated solutions of a lipophilic drug for dermal delivery, International Journal of Pharmaceutics, 224: 169-176.
-
International Journal of Pharmaceutics
, vol.224
, pp. 169-176
-
-
Moser, K.1
Kriwet, K.2
Kalia, Y.N.3
Guy, R.H.4
-
9
-
-
0014824052
-
Acyloxymethyl esters of ampicillin
-
Daehne W. V., Frederiksen E., Gundersen E., Lund F., Morch P., Peterson H. J., Roholt K., Trybring L., Godtfredsen W., Acyloxymethyl esters of ampicillin, J. Med. Chem., 1970, 13, 607-612.
-
(1970)
J. Med. Chem
, vol.13
, pp. 607-612
-
-
Daehne, W.V.1
Frederiksen, E.2
Gundersen, E.3
Lund, F.4
Morch, P.5
Peterson, H.J.6
Roholt, K.7
Trybring, L.8
Godtfredsen, W.9
-
10
-
-
77953368587
-
-
ANDA, Manufacturing and control Information, Central Drug Evaluation and Research CDER
-
ANDA, Pharmaceutical Solid polymorphism Chemistry, Manufacturing and control Information, Central Drug Evaluation and Research (CDER), 2007.
-
(2007)
Pharmaceutical Solid polymorphism Chemistry
-
-
-
11
-
-
77953366465
-
-
Derle D. V., Bele M., Kasliwal N., In vitro and in vivo evaluation of mefenamic acid and its complexes with β-Cyclodextrin and HP-β-Cyclodextrin, Asian Journal of Pharmaceutics, 2008, 2, 30-34.
-
(2008)
In vitro and in vivo evaluation of mefenamic acid and its complexes with β-Cyclodextrin and HP-β-Cyclodextrin, Asian Journal of Pharmaceutics
, vol.2
, pp. 30-34
-
-
Derle, D.V.1
Bele, M.2
Kasliwal, N.3
-
12
-
-
0342702115
-
Effect of dosage form on drug absorption. A frequent variable in clinical pharmacology
-
Levy G., Effect of dosage form on drug absorption. A frequent variable in clinical pharmacology, Arch. Int. Pharmacodyn. Ther., 1964, 152, 59-68.
-
(1964)
Arch. Int. Pharmacodyn. Ther
, vol.152
, pp. 59-68
-
-
Levy, G.1
-
13
-
-
0000625698
-
Physicochemical properties of 1-(3,4-dimethoxyphenyl) -2,3-bis-(methoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynapthalene, a new hypo cholesterolemic agent, and its gastrointestinal absorption in dogs
-
Kubo H., Mizobe M., Physicochemical properties of 1-(3,4-dimethoxyphenyl) -2,3-bis-(methoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynapthalene, a new hypo cholesterolemic agent, and its gastrointestinal absorption in dogs, Yakuzaigaku, 1995, 55, 244-249.
-
(1995)
Yakuzaigaku
, vol.55
, pp. 244-249
-
-
Kubo, H.1
Mizobe, M.2
-
14
-
-
24744466894
-
Solubility of (±)-ibuprofen and S (+)-ibuprofen in the presence of cosolvents and cyclodextrins
-
Nerurkar J., Beach J. W., Park M. O., Jun H. W., Solubility of (±)-ibuprofen and S (+)-ibuprofen in the presence of cosolvents and cyclodextrins, Pharm. Dev. Technol., 2005, 10, 413-421.
-
(2005)
Pharm. Dev. Technol
, vol.10
, pp. 413-421
-
-
Nerurkar, J.1
Beach, J.W.2
Park, M.O.3
Jun, H.W.4
-
15
-
-
0035991618
-
Examination of the solubilization of drugs by bile salt micelles
-
Wiedmann T. S., Kamel L., Examination of the solubilization of drugs by bile salt micelles, J. Pharm. Sci., 2002, 91, 1743-1764.
-
(2002)
J. Pharm. Sci
, vol.91
, pp. 1743-1764
-
-
Wiedmann, T.S.1
Kamel, L.2
-
16
-
-
8144230197
-
Griseofulvin micronization and dissolution rate improvement by super critical assisted atomization
-
Reverchon E., Dellaporta G., Spade A., Antonacci A., Griseofulvin micronization and dissolution rate improvement by super critical assisted atomization, J. Pharm. Pharmacol., 2004, 56, 1379-1387.
-
(2004)
J. Pharm. Pharmacol
, vol.56
, pp. 1379-1387
-
-
Reverchon, E.1
Dellaporta, G.2
Spade, A.3
Antonacci, A.4
-
17
-
-
1642399085
-
Physicochemical characterization and dissolution properties of meloxicam-cyclodextrin binary systems
-
Naidu N. B., Choudary K. P. R., Murthy K. V. R., Satyanarana V., Hayman A. R., Becket G., Physicochemical characterization and dissolution properties of meloxicam-cyclodextrin binary systems, J. Pharma. Biomed. Anal., 2004, 35: 75-86.
-
(2004)
J. Pharma. Biomed. Anal
, vol.35
, pp. 75-86
-
-
Naidu, N.B.1
Choudary, K.P.R.2
Murthy, K.V.R.3
Satyanarana, V.4
Hayman, A.R.5
Becket, G.6
-
18
-
-
33748209143
-
-
Modi A., Tayade P., Enhancement of Dissolution Profile by Solid Dispersion (Kneading) Technique, AAPS PharmSciTech., 2006, 7 (3), Article 68.
-
Modi A., Tayade P., Enhancement of Dissolution Profile by Solid Dispersion (Kneading) Technique, AAPS PharmSciTech., 2006, 7 (3), Article 68.
-
-
-
-
19
-
-
34347386072
-
Studies on enhancement of dissolution rate of etoposide
-
Raju Y. P., Garbhapu A., Prasanna S. A. L., Rao B. S., Ramana M. K. V., Studies on enhancement of dissolution rate of etoposide, Indian Journal of Pharmaceutical Sciences, 2007, 69, 269-273.
-
(2007)
Indian Journal of Pharmaceutical Sciences
, vol.69
, pp. 269-273
-
-
Raju, Y.P.1
Garbhapu, A.2
Prasanna, S.A.L.3
Rao, B.S.4
Ramana, M.K.V.5
-
20
-
-
77953423668
-
-
US Patent 6756062, Preparation of drug particles using evaporation precipitation into aqueous solutions, US patent, 2004
-
US Patent (6756062), Preparation of drug particles using evaporation precipitation into aqueous solutions, US patent, 2004.
-
-
-
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