Dissolution Profiles of Solid Dispersions Containing Poorly Water-Soluble Drugs and Solubilizing Compositions |
Kim, Tae-Wan
(Biological Rhythm and Controlled Release Lab., College of Pharmacy, Kangwon National University,Pharm Tech Research Incorp.)
Choi, Choon-Young (Biological Rhythm and Controlled Release Lab., College of Pharmacy, Kangwon National University,Pharm Tech Research Incorp.) Cao, Qing-Ri (Biological Rhythm and Controlled Release Lab., College of Pharmacy, Kangwon National University) Kwon, Kyoung-Ae (Handok Pharmaceutical Co., LTD.) Lee, Beom-Jin (Biological Rhythm and Controlled Release Lab., College of Pharmacy, Kangwon National University,Pharm Tech Research Incorp.) |
1 | J.W. Wong, K.H. Yuen, Improved oral bioavailability of artemisinin through inclusion complexation with b- and g-cyclodestrins, Int. J. Pharm., 227, 177-185 (2001) DOI ScienceOn |
2 | A.M. Abdul-Fattah, H.N. Bhargava, Preparation and in vitro evaluation of solid dispersions of halofantrine, Int. J. Pharm., 235, 17-33 (2002) DOI ScienceOn |
3 | S.R. Vippagunta, K.A. Maul, S. Tallavajhala, Solid-state characterization of nifedipine solid dispersions, Int. J. Pharm., 236, 111-123 (2002) DOI ScienceOn |
4 | A. Acharya, S. K. Sanyal and S. P. Moulik, Physicochemical investigations on microemulsification of eucalyptol and water in presence of polyoxyethylene (4) lauryl ether (Brij-30) and ethanol, Int. J. Pharm., 229, 213-226 (2001) DOI ScienceOn |
5 | S. M. Khoo, A. J. Humberstone, C. J. H. Porter, G. A. Edwards and W. N. Charman, Formulation design and bioavailability assessment of lipidic self-emulsifying formulations of halo- fantrine, Int. J. Pharm., 167, 155-164 (1998) DOI ScienceOn |
6 | A. Billon, B. Bataille, G. Cassanas and M. Jacob, Develop- ment of spray-dried acetaminophen microparticles using experimental designs, Int. J. Pharm., 203, 159-168 (2000) DOI ScienceOn |
7 | E. Broman, C. Khoo, L.S. Taylor, A comparison of alterna- tive polymer excipients and processing methods for making solid dispersions of a poorly water soluble drug, Int. J. Pharm., 222, 139-151 (2001) DOI ScienceOn |
8 | M. O. Omelczuk, C. C. Wang, and D. G. Pope, Influence of miconization on the compaction properties of an inve-stigational drug using tableting index analysis, Eur. J. Pharm. Biopharm., 148, 123-130 (1997) |
9 | J.M. Aceves, R. Cruz, and E. Hernandez, Preparation and characterization of furosemide-eudragit controlled release systems, Int. J. Pharm., 195, 45-53 (2000) DOI ScienceOn |
10 | V. Agarwal, I.K. Reddy and M.A. Khan, Polymethyacrylate based microparticulates of insulin for oral delivery: Preparation and in vitro dissolution stability in the presence of enzyme inhibitors, Int. J. Pharm., 225, 31-39 (2001) DOI ScienceOn |
11 | N. Zerrouk, C. Chemtob, P. Arnaud, and S. Toscani, In vitro and in vivo evaluation of carbamazepine-PEG 6000 solid dispersions, Int. J. Pharm., 225, 49-62 (2001) DOI ScienceOn |
12 | A. Zornoza, C. Martin, M. Sanchez, I. Velaz and A. Piquer, Inclusion complexation of glisentide with -,- and -cyclodextrins, Int. J. Pharm., 169, 239-244 (1998) DOI ScienceOn |
13 | D.Q.M Craig, The mechanisms of drug release from solid dispersions in water-soluble polymers, Int. J. Pharm., 231, 131-144 (2002) DOI ScienceOn |