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首页> 外文期刊>Journal of Materials Science. Materials in Medicine >Controlled release of insulin from PLGA nanoparticles embedded within PVA hydrogels
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Controlled release of insulin from PLGA nanoparticles embedded within PVA hydrogels

机译:从PVA水凝胶中嵌入的PLGA纳米颗粒中控制释放胰岛素

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摘要

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 intraperi-toneally as a single dose (20 U/kg) to streptozotocin-in-duced 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.
机译:成功地构建了一个简单而通用的肽和蛋白质递送平台,该平台基于包含胰岛素负载的聚乳酸-乙醇酸(PLGA)纳米粒子的物理交联的聚乙烯醇(PVA)水凝胶,从而成功地实现了这一目标。用SEM和激光散射法分别表征了颗粒的形貌和尺寸。结果表明,这些颗粒的平均直径为615 nm,具有窄的粒度分布和均匀的颗粒产生。蛋白质的包封率为72.6%。当将负荷胰岛素的PLGA纳米颗粒以单剂量(20 U / kg)腹腔内给药于链脲佐菌素诱导的糖尿病小鼠时,这些小鼠的血糖水平降低,并且可以维持这种水平超过24小时。体外释放进一步表明,纳米颗粒截留在PVA水凝胶中会导致释放速率和释放的胰岛素总量降低,这表明截留在PVA水凝胶中的PLGA纳米颗粒显示出更合适的蛋白质释放控制动力学。

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