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用于血管内皮生长因子递送的聚乳酸-羟基乙酸共聚物/碳量子点微球的微流控合成

Microfluidic synthesis of PLGA/carbon quantum dot microspheres for vascular endothelial growth factor delivery.

作者信息

Omidi Meisam, Hashemi Mohadeseh, Tayebi Lobat

机构信息

Marquette University School of Dentistry Milwaukee WI USA

Department of Biomedical Engineering, The University of Texas at Austin Austin USA.

出版信息

RSC Adv. 2019 Oct 17;9(57):33246-33256. doi: 10.1039/c9ra06279c. eCollection 2019 Oct 15.

Abstract

In this study, vascular endothelial growth factor (VEGF) loaded poly(d,l-lactide--glycolide) (PLGA) - carbon quantum dot microspheres were produced using microfluidic platforms. The microcapsules were fabricated in flow-focusing geometry with a biphasic flow to generate solid/oil/water (s-o-w) droplets. To avoid any damage to protein functional and structural stability during the encapsulation process, the VEGF was PEGylated. The produced microspheres were intact and highly monodisperse in size (CV < 5%). Furthermore, microspheres in a size range of 16-36 µm were achieved by adjusting the flow ratio parameter. The encapsulation efficiency, release profile, and bioactivity of the produced microparticles were also studied. The loading efficiency of PEGylated VEGF in the microparticles was varied from 51-69% and more than 90% of PEGylated VEGF was released within 28 days. Furthermore, the release of VEGF was indirectly monitored by carbon quantum dots. The present monodisperse and controllable VEGF loaded microspheres with reproducible manner could be widely used in tissue engineering and therapeutic applications.

摘要

在本研究中,使用微流控平台制备了负载血管内皮生长因子(VEGF)的聚(d,l-丙交酯-乙交酯)(PLGA)-碳量子点微球。微胶囊采用双相流的流动聚焦几何结构制备,以产生固/油/水(s-o-w)液滴。为避免在包封过程中对蛋白质功能和结构稳定性造成任何损害,对VEGF进行了聚乙二醇化修饰。所制备的微球完整且尺寸高度均一(变异系数<5%)。此外,通过调节流速比参数获得了尺寸范围为16-36 µm的微球。还研究了所制备微粒的包封效率、释放曲线和生物活性。微粒中聚乙二醇化VEGF的负载效率在51%-69%之间,超过90%的聚乙二醇化VEGF在28天内释放。此外,通过碳量子点间接监测VEGF的释放。目前这种具有可重复方式的单分散且可控的负载VEGF微球可广泛应用于组织工程和治疗应用。

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