蛋白缓释透明质酸酪胺微凝胶的合成

Elaheh Jooybar, M. Abdekhodaie, P. Dijkstra
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引用次数: 1

摘要

微凝胶是一种高含水量的亲水聚合物基质,适用于生物分子的包封和递送。本研究采用油包水乳化法合成透明质酸微凝胶。首先用酪胺修饰透明质酸,然后将聚合物溶液以异辛烷为油相均质制备微乳液。以辣根过氧化物酶(酶)和过氧化氢为原料,采用酶促交联的方法制备了稳定的HA微滴,交联反应温和。结果表明,增加初始聚合物浓度可以获得更大的微凝胶。将牛血清白蛋白(BSA)和溶菌酶两种样品蛋白加入到聚合物网络中,研究微凝胶的包封效率。结果表明,该方法具有较高的蛋白包封效率(> 70%)。释放谱显示,溶菌酶作为一种阳离子蛋白,在两周内持续释放。而牛血清白蛋白作为带负电荷的蛋白,其释放速度更快。制备微凝胶的简单方法,以及被包裹的蛋白质的持续释放,使透明质酸微凝胶成为一种很有前途的阳离子蛋白质递送载体。
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Synthesis of Hyaluronic acid-Tyramine Microgels for Sustained Protein Release
Microgels are hydrophilic polymer matrix with high water content suitable for encapsulation and delivery of biomolecules. In this study, hyaluronic acid (HA) microgels were synthesized using a water in oil emulsion method. First, hyaluronic acid was modified with tyramine, and then the microemulsion was produced by homogenizing the polymer solution in isooctane as an oil phase. HA microdroplets were crosslinked via enzymatic method by addition of horseradish peroxidase (enzyme) and hydrogen peroxide, and stable microgels were produced in a mild crosslinking reaction. According to the results, larger microgels were achieved by increasing the initial polymer concentration. Two sample proteins, Bovine serum albumin (BSA) and lysozyme, were incorporated in the polymer network to investigate the encapsulation efficiency of the microgels. The results demonstrated that the proposed method has a high efficiency for protein encapsulation (> 70%). The release profiles showed that lysozyme, as a cationic protein, was released in a sustained manner over a period of two weeks. However, BSA, as a negatively charged protein, showed a faster release rate. The simple method of microgel fabrication, besides the sustained release of the encapsulated proteins, makes the HA microgels a promising vehicle for delivery of cationic proteins.
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