Increased physical stability and improved dissolution properties of itraconazole, a class II drug, by solid dispersions that combine fast- and slow-dissolving polymers. Export

@article{citeulike:490862, abstract = {Solid dispersions were prepared of itraconazole-Eudragit E100, itraconazole-PVPVA64, and itraconazole-Eudragit E100/PVPVA64 using a corotating twin-screw hot-stage extruder. Modulated temperature differential scanning calorimetry (MTDSC) was used to evaluate the miscibility of the extrudates, and dissolution experiments were performed in simulated gastric fluid without pepsin (SGF(sp)). Itraconazole and Eudragit E100 are miscible up to 13\% w/w drug loading. From that concentration on, phase separation is observed. Pharmaceutical performance of this dispersion was satisfactory because 80\% of the drug dissolved after 30 min. Extrudates of itraconazole and PVPVA64 were completely miscible but the pharmaceutical performance was low, with 45\% of drug dissolved after 3 h. Combination of both polymers in different ratios, with a fixed drug loading of 40\% w/w, was evaluated. MTDSC results clearly indicated a two-phase system consisting of itraconazole-Eudragit E100 and itraconazole-PVPVA64 phases. In these extrudates, no free crystalline or glassy clusters of itraconazole were observed; all itraconazole was mixed with one of both polymers. The pharmaceutical performance was tested in SGF(sp) for different polymer ratios, and Eudragit E100/PVPVA64 ratios of 50/50 and 60/40 showed significant increases in dissolution rate and level. Polymer ratios of 70/30 and 80/20, on the other hand, had a release of 85\% after 30 min. Precipitation of the drug was never observed. The combination of the two polymers provides a solid dispersion with good dissolution properties and improved physical stability compared with the binary solid dispersions of itraconazole.}, address = {Laboratorium voor Farmacotechnologie en Biofarmacie, Campus Gasthuisberg O + N, 49 Herestraat, Leuven, B-3000 Belgium.}, author = {Six, K. and Verreck, G. and Peeters, J. and Brewster, M. and Van Den Mooter, G.}, citeulike-article-id = {490862}, citeulike-linkout-0 = {http://dx.doi.org/10.1002/jps.10522}, citeulike-linkout-1 = {http://view.ncbi.nlm.nih.gov/pubmed/14648642}, citeulike-linkout-2 = {http://www.hubmed.org/display.cgi?uids=14648642}, doi = {10.1002/jps.10522}, issn = {0022-3549}, journal = {J Pharm Sci}, keywords = {extrusion, hot, melt}, month = {January}, number = {1}, pages = {124--131}, posted-at = {2006-02-03 10:09:05}, priority = {3}, title = {Increased physical stability and improved dissolution properties of itraconazole, a class II drug, by solid dispersions that combine fast- and slow-dissolving polymers.}, url = {http://dx.doi.org/10.1002/jps.10522}, volume = {93}, year = {2004} }

TY - JOUR ID - citeulike:490862 L3 - citeulike-article-id:490862 N2 - Solid dispersions were prepared of itraconazole-Eudragit E100, itraconazole-PVPVA64, and itraconazole-Eudragit E100/PVPVA64 using a corotating twin-screw hot-stage extruder. Modulated temperature differential scanning calorimetry (MTDSC) was used to evaluate the miscibility of the extrudates, and dissolution experiments were performed in simulated gastric fluid without pepsin (SGF(sp)). Itraconazole and Eudragit E100 are miscible up to 13% w/w drug loading. From that concentration on, phase separation is observed. Pharmaceutical performance of this dispersion was satisfactory because 80% of the drug dissolved after 30 min. Extrudates of itraconazole and PVPVA64 were completely miscible but the pharmaceutical performance was low, with 45% of drug dissolved after 3 h. Combination of both polymers in different ratios, with a fixed drug loading of 40% w/w, was evaluated. MTDSC results clearly indicated a two-phase system consisting of itraconazole-Eudragit E100 and itraconazole-PVPVA64 phases. In these extrudates, no free crystalline or glassy clusters of itraconazole were observed; all itraconazole was mixed with one of both polymers. The pharmaceutical performance was tested in SGF(sp) for different polymer ratios, and Eudragit E100/PVPVA64 ratios of 50/50 and 60/40 showed significant increases in dissolution rate and level. Polymer ratios of 70/30 and 80/20, on the other hand, had a release of 85% after 30 min. Precipitation of the drug was never observed. The combination of the two polymers provides a solid dispersion with good dissolution properties and improved physical stability compared with the binary solid dispersions of itraconazole. IS - 1 JF - J Pharm Sci SN - 0022-3549 AD - Laboratorium voor Farmacotechnologie en Biofarmacie, Campus Gasthuisberg O + N, 49 Herestraat, Leuven, B-3000 Belgium. EP - 131 TI - Increased physical stability and improved dissolution properties of itraconazole, a class II drug, by solid dispersions that combine fast- and slow-dissolving polymers. VL - 93 SP - 124 KW - extrusion KW - hot KW - melt AU - Six, K AU - Verreck, G AU - Peeters, J AU - Brewster, M AU - Van Den Mooter, G PY - 2004/01// UR - http://dx.doi.org/10.1002/jps.10522 ER -