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Silk fibroin as a novel coating material for controlled release of theophylline

机译:丝素蛋白作为新型茶碱控释包衣材料

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摘要

The aim of this study was to explore potential use of the silk fibroin (SF) as an aqueous coating material for theophylline tablets. We have examined the film forming and coating properties of heat-treated fibroin, SF solution having different amounts of polyethylene glycol (PEG) and 1-ethyl-3-(3-dimethyl aminopropyl)carbodiimide (EDC) cross-linked SF. Heat-treated SF material possessed a brittle structure, which resulted in poor film forming and coating properties. The optimum PEG amount in SF solution was determined as 17% (by weight) for an acceptable film forming and zero order release profile. EDC cross-linked SF has shown a very good film forming and coating property with a potential for sustaining the drug release from coated theophylline tablets. Dissolution data for coated theophylline tablets were analyzed using Ritger and Peppas equation to describe the mechanism of drug release. Drug release from the EDC coated tablets followed zero-order kinetics. Release rate constants were found to be 0.26, 0.19, 0.16% min-1 for single-coated, double coated, and triple coated tablets, respectively. These results clearly demonstrated that silk fibroin has high utility as a novel aqueous coating material for controlled release products.
机译:这项研究的目的是探索丝素蛋白(SF)作为茶碱片的水性包衣材料的潜在用途。我们已经检查了具有不同量的聚乙二醇(PEG)和1-乙基-3-(3-二甲基氨基丙基)碳二亚胺(EDC)交联SF的热处理丝蛋白,SF溶液的成膜和涂层性能。热处理的SF材料具有脆性结构,导致较差的成膜性和涂层性。对于可接受的膜形成和零级释放曲线,将SF溶液中的最佳PEG量确定为17%(重量)。 EDC交联的SF已显示出非常好的成膜性和包衣性,并具有维持药物从包衣茶碱片中释放的潜力。使用Ritger和Peppas方程分析包衣茶碱片的溶出度数据,以描述药物释放的机理。从EDC包衣片剂释放的药物遵循零级动力学。发现单包衣,双包衣和三包衣的片剂的释放速率常数分别为0.26、0.19、0.16%min-1。这些结果清楚地表明,丝素蛋白作为控释产品的新型水性包衣材料具有很高的实用性。

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