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首页> 外文期刊>Colloid and polymer science >Encapsulation of proteinase K in PEL A ultrafine fibers by emulsion electrospinning: preparation and in vitro evaluation
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Encapsulation of proteinase K in PEL A ultrafine fibers by emulsion electrospinning: preparation and in vitro evaluation

机译:乳液静电纺丝法将蛋白酶K包裹在PEL A超细纤维中:制备和体外评价

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The aims of this study were to encapsulate water-soluble bioactive agents into biodegradable hydrophobic polymers via emulsion electrospinning for drug delivery and tissue engineering applications and propose a simple and facile method to evaluate the bioactivity of the encapsulated protein. Proteinase K was selected as a model protein to be incorporated into poly(ethylene glycol)-poly (L-lactide) (PELA) ultrafine fibers. Core-shell structured fibers with single core or multi-core were observed. In vitro release study showed that after a burst release at the early stage, a sustained release was achieved, indicating that proteinase K was incorporated inside ultrathin fibers successfully. Results of in vitro incubation in Tris-HCl buffer at pH8.6 and 37°C revealed that electrospun PELA membranes containing proteinase K (PELA-P) showed obvious morphological changes, large mass loss, and slight decreases in melting temperature, melting enthalpy and relative molecular mass in 7 days. Additionally, a significant drop in pH value of the buffer after incubation of the PELA-P membrane was also observed. These findings clearly showed that encapsulation of water-soluble bioactive agents inside hydrophobic polymers could be achieved by emulsion electrospinning without compromising their bioactivity.
机译:这项研究的目的是通过乳液静电纺丝将水溶性生物活性剂封装到可生物降解的疏水性聚合物中,以用于药物输送和组织工程应用,并提出一种简单而简便的方法来评估封装的蛋白质的生物活性。选择蛋白酶K作为模型蛋白,以掺入聚(乙二醇)-聚(L-丙交酯)(PELA)超细纤维中。观察到具有单核或多核的核-壳结构纤维。体外释放研究表明,在早期爆发释放后,实现了持续释放,这表明蛋白酶K已成功掺入超薄纤维内。在pH8.6和37°C的Tris-HCl缓冲液中进行体外培养的结果表明,含有蛋白酶K的电纺PELA膜(PELA-P)表现出明显的形态变化,质量损失大,熔融温度,熔融焓和熔融温度略有降低7天的相对分子质量。另外,还观察到在孵育PELA-P膜后缓冲液的pH值显着下降。这些发现清楚地表明,通过乳液静电纺丝可以在不损害其生物活性的情况下将水溶性生物活性剂包裹在疏水性聚合物中。

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