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丝素微球作为人重组 BMPs 的载体。物理特性表征和药物释放。

Silk fibroin microparticles as carriers for delivery of human recombinant BMPs. Physical characterization and drug release.

机构信息

3B's Research Group - Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, Ave Park, 4806-909 Taipas, Guimarães, Portugal.

出版信息

J Tissue Eng Regen Med. 2010 Jul;4(5):349-55. doi: 10.1002/term.245.

Abstract

Bone morphogenetic proteins (BMPs) are cytokines with strong ability to promote new bone formation. Herein, we report the use of silk fibroin microparticles as carriers for the delivery of BMP-2, BMP-9 or BMP-14. BMP-containing fibroin microparticles were prepared by a mild methodology using dropwise addition of ethanol, exhibiting mean diameters of 2.7 +/- 0.3 microm. Encapsulation efficiencies varied between 67.9 +/- 6.1 % and 97.7 +/- 2.0 % depending on the type and the amount of BMP loaded. Release kinetics showed that BMP-2, BMP-9 and BMP-14 were released in two phases profile, with a burst release in the first two days followed by a slower release, for a period of 14 days. The release data were best explained by Korsmeyer's model and the Fickian model of drug diffusion. Silk fibroin microparticles can offer a promising approach for the sustained delivery of different BMPs in tissue engineering applications.

摘要

骨形态发生蛋白(BMPs)是具有强烈促进新骨形成能力的细胞因子。在此,我们报告了使用丝素蛋白微球作为载体来递送 BMP-2、BMP-9 或 BMP-14。通过使用乙醇逐滴添加的温和方法制备了含 BMP 的丝素蛋白微球,其平均直径为 2.7 +/- 0.3 微米。根据负载的 BMP 的类型和数量,包封效率在 67.9 +/- 6.1%至 97.7 +/- 2.0%之间变化。释放动力学表明,BMP-2、BMP-9 和 BMP-14 以两相释放曲线释放,在最初两天有一个突释,然后是一个较慢的释放,持续 14 天。释放数据最好通过 Korsmeyer 模型和药物扩散的 Fickian 模型来解释。丝素蛋白微球可为组织工程应用中不同 BMP 的持续递送提供一种有前途的方法。

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