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Stimuli-Sensitive Hydrogel Based on N-Isopropylacrylamide and Itaconic Acid for Entrapment and Controlled Release of Candida rugosa Lipase under Mild Conditions

机译:基于N-异丙基丙烯酰胺和衣康酸的刺激敏感水凝胶在温和条件下可诱捕和控制释放念珠菌脂肪酶

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摘要

Stimuli responsive pH- and temperature-sensitive hydrogel drug delivery systems, as those based on N-isopropylacrylamide (NiPAAm) and itaconic acid (IA), have been attracting much of the attention of the scientific community nowadays, especially in the field of drug release. By adjusting comonomer composition, the matrix is enabled to protect the incorporated protein in the highly acidic environment of upper gastrointestinal tract and deliver it in the neutral or slightly basic region of the lower intestine. The protein/poly(NiPAAm-co-IA) hydrogels were synthetized by free radical crosslinking copolymerization and were characterized concerning their swelling capability, mechanical properties, and morphology. The pore structure and sizes up to 1.90 nm allowed good entrapment of lipase molecules. Model protein, lipase from Candida rugosa, was entrapped within hydrogels upon mild conditions that provided its protection from harmful environmental influences. The efficiency of the lipase entrapment reached 96.7%, and was dependent on the initial concentration of lipase solution. The swelling of the obtained hydrogels in simulated pH and temperature of gastrointestinal tract, the lipase entrapment efficiency, and its release profiles from hydrogels were investigated as well.
机译:像基于N-异丙基丙烯酰胺(NiPAAm)和衣康酸(IA)的刺激响应pH和温度敏感的水凝胶药物传递系统,如今引起了科学界的广泛关注,尤其是在药物释放领域。通过调节共聚单体的组成,基质能够在上胃肠道的高酸性环境中保护掺入的蛋白质,并将其输送到下肠的中性或弱碱性区域。通过自由基交联共聚合成蛋白质/聚(NiPAAm-co-IA)水凝胶,并对其溶胀能力,机械性能和形态进行了表征。孔结构和最大1.90 1.nm的尺寸允许脂肪酶分子良好的包封。在温和条件下,模型蛋白(来自假丝酵母(Candida rugosa)的脂肪酶)被截留在水凝胶中,从而保护其免受有害环境的影响。脂肪酶截留的效率达到96.7%,并取决于脂肪酶溶液的初始浓度。还研究了获得的水凝胶在胃肠道的pH和温度下的溶胀,脂肪酶的包封效率及其从水凝胶中的释放曲线。

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