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首页> 外文期刊>Indian journal of pharmaceutical sciences. >Design and Development of Mixed Film of Pectin: Ethyl Cellulose for Colon Specific Drug Delivery of Sennosides and Triphala
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Design and Development of Mixed Film of Pectin: Ethyl Cellulose for Colon Specific Drug Delivery of Sennosides and Triphala

机译:果胶:乙基纤维素混合膜的设计与开发:用于人参皂苷和三叶草的结肠特异性药物递送

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摘要

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.
机译:本研究旨在开发针对番石榴苷和Triphala的结肠特异性药物递送系统。这些药物是印度著名的用于便秘的印度草药。拟议的设备探索了果胶和乙基纤维素作为结肠特异性递送的混合膜的应用。该混合膜是使用非水溶剂如丙酮和异丙醇制备的。采用32因子设计来优化配方变量,例如乙基纤维素与果胶的比例(X1)和涂层重量(X2)。发现药物释放的速率和程度与膜中果胶与乙基纤维素的厚度和比例有关。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,含有更高比例果胶的涂料配方的药物释放更为明显。装置的表面涂有Eudragit S100,以确保该装置对pH的依赖性更大,并且仅在较高pH时触发药物释放。预期最终产品具有可生物降解和依赖pH的优势。这种类型的薄膜可有效释放药物,同时保持其完整性。

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