Development and Optimization of Self-emulsifying Drug Delivery Systems (SEDDS) for Enhanced Dissolution and Permeability of Rosuvastatin
Makaleler > Tam Makale · 2016
Yazarlar: Hatice Yeşim KARASULU, Evren ATLIHAN GÜNDOĞDU, T. Turgay, U. O. Turk, S. Apaydin, Ilgın YILDIRIM ŞİMŞİR, C. Yilmaz, Ercüment KARASULU
Current Drug Delivery, SCI Expanded İndekslerine Giren Dergi, Uluslararası, Wos, 2016, cilt 13, ss 362-370
DOI: 10.2174/156720181303160520211640
Özet
Rosuvastatin calcium is commonly used statin for treatment of dyslipidemia. It has low bioavailability. The aim of this study was to develop new rosuvastatin calcium self-emulsifying drug delivery systems (SEDDS) as an alternative formulation and to evaluate the permeability of rosuvastatin calcium SEDDS by using Caco-2 cells. Rosuvastatin calcium SEDDSs were developed by using pseudo ternary phase diagram and characterized by using heating cooling cycle, robustness to dilution, stability and in vitro drug release and permeability. The permeability studies of rosuvastatin calcium SEDDS (Papp (A→B) for F1-RS=1.492×10-5±0.413×10-5 and Papp (A→B) for F2-RS=1.254×10-5±0.19×10-5) across Caco-2 cells showed that permeability value from apical to basolateral was higher than permeability value of commercial formulation (Papp (A→B) =7.13×10-5±0.668×10-5). In conclusion, SEDDS as a drug carrier may be used as an effective and alternative hyperlipidemia therapy for oral delivery of rosuvastatin calcium.