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胰岛素从嵌入聚乙烯醇水凝胶中的聚乳酸-羟基乙酸共聚物纳米颗粒中的控释。

Controlled release of insulin from PLGA nanoparticles embedded within PVA hydrogels.

作者信息

Liu J, Zhang S M, Chen P P, Cheng L, Zhou W, Tang W X, Chen Z W, Ke C M

机构信息

Advanced Biomaterials and Tissue Engineering Center, Huazhong University of Science and Technology, Wuhan 430074, China.

出版信息

J Mater Sci Mater Med. 2007 Nov;18(11):2205-10. doi: 10.1007/s10856-007-3010-0. Epub 2007 Aug 1.

Abstract

A simple and versatile delivery platform for peptide and protein based on physically cross-linked poly (vinyl alcohol) (PVA) hydrogels containing insulin-loaded poly (lactic-co-glycolic acid) (PLGA) nanoparticles was successfully fabricated. The particle morphology and size were characterized by SEM and laser light scattering method, respectively. Results showed that these particles had a mean diameter of 615 nm with a narrow size distribution and homogeneous particle production. The protein encapsulation efficiency was 72.6%. When insulin-loaded PLGA nanoparticles were administered intraperitoneally as a single dose (20 U/kg) to streptozotocin-induced diabetic mouse, blood glucose levels of these mice decreased and it could be sustained at such levels over 24 h. In vitro release further indicated that entrapment of the nanoparticles into the PVA hydrogels causes a reduction in both the release rate and the total amount of insulin released, which suggesting that PLGA nanoparticles entrapped into the PVA hydrogels showed more suitable controlled release kinetics for protein delivery.

摘要

基于含有负载胰岛素的聚乳酸-乙醇酸共聚物(PLGA)纳米颗粒的物理交联聚乙烯醇(PVA)水凝胶,成功制备了一种简单且通用的肽和蛋白质递送平台。分别通过扫描电子显微镜(SEM)和激光散射法对颗粒形态和尺寸进行了表征。结果表明,这些颗粒的平均直径为615 nm,粒径分布窄且颗粒生成均匀。蛋白质包封率为72.6%。当将负载胰岛素的PLGA纳米颗粒以单剂量(20 U/kg)腹腔注射给链脲佐菌素诱导的糖尿病小鼠时,这些小鼠的血糖水平下降,并且在24小时内可维持在该水平。体外释放进一步表明,将纳米颗粒包封到PVA水凝胶中会导致胰岛素释放速率和释放总量降低,这表明包封在PVA水凝胶中的PLGA纳米颗粒在蛋白质递送方面表现出更合适的控释动力学。

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