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通过不同的聚己内酯表面修饰来改变壳聚糖纳米凝胶功能化的聚己内酯纤维垫中 BMP-2 的持续释放。

Varying the sustained release of BMP-2 from chitosan nanogel-functionalized polycaprolactone fiber mats by different polycaprolactone surface modifications.

机构信息

Technische Universität Braunschweig, Institut für Pharmazeutische Technologie und Biopharmazie, Braunschweig, Germany.

Technische Universität Braunschweig, Institut für Technische Chemie, Braunschweig, Germany.

出版信息

J Biomed Mater Res A. 2021 May;109(5):600-614. doi: 10.1002/jbm.a.37045. Epub 2020 Jul 14.

Abstract

Polycaprolactone (PCL) fiber mats with different surface modifications were functionalized with a chitosan nanogel coating to attach the growth factor human bone morphogenetic protein 2 (BMP-2). Three different hydrophilic surface modifications were compared with regard to the binding and in vitro release of BMP-2. The type of surface modification and the specific surface area derived from the fiber thickness had an important influence on the degree of protein loading. Coating the PCL fibers with polydopamine resulted in the binding of the largest BMP-2 quantity per surface area. However, most of the binding was irreversible over the investigated period of time, causing a low release in vitro. PCL fiber mats with a chitosan-graft-PCL coating and an additional alginate layer, as well as PCL fiber mats with an air plasma surface modification boundless BMP-2, but the immobilized protein could almost completely be released. With polydopamine and plasma modifications as well as with unmodified PCL, high amounts of BMP-2 could also be attached directly to the surface. Integration of BMP-2 into the chitosan nanogel functionalization considerably increased binding on all hydrophilized surfaces and resulted in a sustained release with an initial burst release of BMP-2 without detectable loss of bioactivity in vitro.

摘要

聚己内酯(PCL)纤维垫经过不同的表面改性处理,并用壳聚糖纳米凝胶涂层进行功能化,以附着生长因子人骨形态发生蛋白 2(BMP-2)。比较了三种不同的亲水表面改性方法,以研究 BMP-2 的结合和体外释放情况。表面改性的类型和纤维厚度产生的比表面积对蛋白质负载程度有重要影响。用聚多巴胺对 PCL 纤维进行涂层处理,导致单位面积结合的 BMP-2 数量最多。然而,在研究期间,大部分结合是不可逆的,导致体外释放量较低。具有壳聚糖接枝-PCL 涂层和额外藻酸盐层的 PCL 纤维垫以及经过空气等离子体表面改性的 PCL 纤维垫能够无限制地结合 BMP-2,但固定的蛋白质几乎可以完全释放。使用聚多巴胺和等离子体改性以及未改性的 PCL,也可以直接将大量 BMP-2 附着到表面上。将 BMP-2 整合到壳聚糖纳米凝胶功能化中,显著增加了所有亲水化表面上的结合,并导致初始突释后持续释放 BMP-2,而体外检测不到生物活性损失。

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