Momin Munira, Pundarikakshudu K, Nagori S A
L. J. Institute of Pharmacy, Sanand Cross Road, Sarkhej Gandhinagar Highway, Ahmedabad-382 210, India.
Indian J Pharm Sci. 2008 May-Jun;70(3):338-43. doi: 10.4103/0250-474X.42998.
The present study was aimed at developing colon specific drug delivery system for sennosides and Triphala. These drugs are reputed Ayurvedic medicines for constipation in India. The proposed device explored the application of pectin and ethyl cellulose as a mixed film for colon specific delivery. This mixed film was prepared using non-aqueous solvents like acetone and isopropyl alcohol. A 32 factorial design was adopted to optimize the formulation variables like, ratio of ethyl cellulose to pectin (X1) and coat weight (X2). The rate and extent of drug release were found to be related to the thickness and the ratio of pectin to ethyl cellulose within the film. Statistical treatments to the drug release data revealed that the X1 variable was more important than X2. Under simulated colonic conditions, drug release was more pronounced from coating formulations containing higher proportions of pectin. The surface of the device was coated with Eudragit S100 to ensure that the device was more pH dependent and trigger the drug release only at higher pH. The final product is expected to have the advantage of being biodegradable and pH dependant. This type of a film effectively releases the drug while maintaining its integrity.
本研究旨在开发用于番泻苷和三果木的结肠靶向给药系统。这些药物在印度是著名的治疗便秘的阿育吠陀药物。所提出的装置探索了将果胶和乙基纤维素用作结肠靶向递送的混合膜。该混合膜使用丙酮和异丙醇等非水溶剂制备。采用32析因设计来优化制剂变量,如乙基纤维素与果胶的比例(X1)和包衣重量(X2)。发现药物释放速率和程度与膜内果胶与乙基纤维素的比例及厚度有关。对药物释放数据的统计处理表明,X1变量比X2更重要。在模拟结肠条件下,含较高比例果胶的包衣制剂药物释放更显著。该装置表面涂有尤特奇S100,以确保该装置对pH更敏感,仅在较高pH值时触发药物释放。预期最终产品具有可生物降解和pH依赖性的优点。这种类型的膜在保持其完整性的同时能有效释放药物。