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首页> 外文期刊>Journal of biomedical materials research, Part A >Varying the sustained release of BMP-2 from chitosan nanogel-functionalized polycaprolactone fiber mats by different polycaprolactone surface modifications
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Varying the sustained release of BMP-2 from chitosan nanogel-functionalized polycaprolactone fiber mats by different polycaprolactone surface modifications

机译:通过不同的聚己内酯表面改性,改变壳聚糖纳米凝胶官能化的聚己内酯纤维垫的持续释放BMP-2

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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.
机译:采用壳聚糖纳米凝胶涂层对具有不同表面修饰的聚己内酯(PCL)纤维垫进行功能化,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性表面修饰对BMP-2结合和体外释放的影响。表面改性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。在PCL纤维上涂覆聚多巴胺可使每表面积结合最大量的BMP-2。然而,在所研究的时间段内,大多数结合是不可逆的,导致体外释放较低。具有壳聚糖接枝PCL涂层和附加海藻酸钠层的PCL纤维垫,以及具有空气等离子体表面修饰的无边界BMP-2的PCL纤维垫,但固定化的蛋白质几乎可以完全释放。通过多多巴胺和血浆修饰以及未修饰的PCL,大量BMP-2也可以直接附着到表面。将BMP-2整合到壳聚糖纳米凝胶功能化中显著增加了对所有亲水表面的结合,并导致BMP-2的持续释放,初始释放时不会在体外检测到生物活性的损失。

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