壳聚糖-卡拉胶聚电解质复合物用于蛋白质药物的递送

Cunben Li, S. Hein, Kean Wang
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引用次数: 38

摘要

采用盐诱导阻聚法制备壳聚糖-卡拉胶聚电解质复合物(PEC),并用牛血清白蛋白(BSA)包封,研究其在pH响应性蛋白类药物口服递送中的应用潜力。FTIR光谱显示在实验条件下PEC的成功形成。在有消化酶和不含消化酶的模拟胃肠道液中研究了牛血清白蛋白的释放动力学。制备的PEC具有ph敏感性。在模拟肠液(SIF, pH 7.5)中,PEC具有典型的控释BSA (3 mg PEC释放180 μg),这是由于PEC明显的肿胀和崩解,而在模拟胃液(SGF, pH 1.2)中,PEC释放少量BSA (3 mg PEC释放11 μg),证实了制备的PEC具有酸性稳定性。发现消化酶的存在不影响PEC对环境pH值的响应,但加速了载体BSA的释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chitosan-Carrageenan Polyelectrolyte Complex for the Delivery of Protein Drugs
A chitosan-carrageenan polyelectrolyte complex (PEC) was prepared by salt induced impeding of polyplex formation method and was encapsulated with bovine serum albumin (BSA) to study the potential to be tailored to the pH responsive oral delivery of protein drugs. The FTIR spectra showed the successful formation of the PEC under the experimental condition. The release kinetics of BSA from the PEC was studied in the simulated gastrointestinal fluids with and without digestive enzymes. The prepared PEC showed the nature of pH-sensitivity. A typical controlled release of BSA from the PEC (180 μg of BSA from 3 mg of PEC) was obtained in the simulated intestinal fluid (SIF, pH 7.5), which was due to the significant swelling and disintegration of PEC, but little amount of BSA was released (11 μg of BSA from 3 mg of PEC) in the simulated gastric fluid (SGF, pH 1.2), confirming acidic stability of the prepared PEC. The presence of digestive enzymes was found not to affect the response of PEC to ambient pH value, but to speed up the release of BSA from carriers.
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