首页> 外文期刊>Journal of Controlled Release: Official Journal of the Controlled Release Society >Hybrid hyaluronan hydrogel encapsulating nanogel as a protein nanocarrier: New system for sustained delivery of protein with a chaperone-like function
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Hybrid hyaluronan hydrogel encapsulating nanogel as a protein nanocarrier: New system for sustained delivery of protein with a chaperone-like function

机译:混合透明质酸水凝胶,将纳米凝胶封装为蛋白质纳米载体:新的系统可持续递送具有伴侣功能的蛋白质

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摘要

Novel hybrid hyaluronan (HA) hydrogel encapsulating nanogels was designed for sustained delivery of protein. HA modified with 2-aminoethyl methacrylate was cross-linked via Michael addition in the presence of cholesteryl group-bearing pullulan (CHP) nanogels. The nanogels were physically entrapped and well dispersed in a three-dimensional network of chemically cross-linked HA (HA gel). Therapeutic peptides and proteins, such as glucagon-like peptide-1, insulin and erythropoietin, were spontaneously trapped in the CHP nanogels in the HA gel just by immersing hybrid hydrogels into the drug solutions. CHP/protein complex nanogels were released from the hybrid hydrogels in a sustained manner both in vitro and in vivo. The release was controlled by the cross-linking density and the degradability of the HA gel, modulated by the initial gelation condition. The synergy between the CHP nanogel as a drug reservoir and the HA gel as a nanogel-releasing matrix of the hybrid hydrogel system simultaneously achieved both simple drug loading and controlled release with no denaturation of the protein drugs. This is a new method of fabricating biodegradable controlled release matrix with molecular chaperone-like activity for therapeutic proteins.
机译:新型混合透明质酸(HA)水凝胶封装纳米凝胶被设计用于蛋白质的持续传递。在带有胆固醇基的支链淀粉(CHP)纳米凝胶的存在下,通过迈克尔加成将甲基丙烯酸2-氨基乙酯改性的HA进行交联。纳米凝胶被物理包裹并很好地分散在化学交联的HA(HA凝胶)的三维网络中。仅通过将杂合水凝胶浸入药物溶液中,即可将治疗性肽和蛋白质(例如胰高血糖素样肽-1,胰岛素和促红细胞生成素)自发捕获在HA凝胶的CHP纳米凝胶中。 CHP /蛋白质复合物纳米凝胶在体外和体内均以持续的方式从杂化水凝胶中释放出来。通过初始凝胶条件调节的HA凝胶的交联密度和降解性来控制释放。 CHP纳米凝胶作为药物储库与HA凝胶作为混合水凝胶系统的纳米凝胶释放基质之间的协同作用同时实现了简单的药物加载和控释,而蛋白质药物没有变性。这是一种制备具有治疗性蛋白质分子伴侣样活性的可生物降解的控释基质的新方法。

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