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可生物降解聚合物泡沫内的无溶剂蛋白质封装

Solvent-free protein encapsulation within biodegradable polymer foams.

作者信息

Hile David D, Pishko Michael V

机构信息

Texas A&M University, Department of Chemical Engineering, College Station, Texas, USA.

出版信息

Drug Deliv. 2004 Sep-Oct;11(5):287-93. doi: 10.1080/10717540490493961.

Abstract

Microporous poly(D,L-lactide-co-glycolide) matrices containing encapsulated proteins were fabricated in a solvent-free manner. Microporous foam was generated by saturating a mixture of polymer and protein particles in supercritical carbon dioxide (SC-CO2), dispersing the protein particles in the polymer melt followed by a rapid evaporation of the CO2 phase. The release rates of protein encapsulated within porous poly(lactide-co-glycolide)(PLGA) constructs produced in SC-CO2 were measured in vitro. Although a substantial amount of protein was released within the first 48 h, results indicated that protein may be dispersed throughout the polymer phase and released over 3 weeks using this solvent-free technique. Basic fibroblast growth factor (bFGF), known to promote angiogenesis in vivo, was encapsulated within the polymer matrix. In addition, retention of biological activity was measured for bFGF encapsulated within PLGA foams. Encapsulated bFGF was released from the porous constructs for up to 10 days in vitro with little loss of biological activity.

摘要

含有包封蛋白质的微孔聚(D,L-丙交酯-共-乙交酯)基质以无溶剂方式制备。通过在超临界二氧化碳(SC-CO₂)中使聚合物和蛋白质颗粒的混合物饱和,将蛋白质颗粒分散在聚合物熔体中,随后快速蒸发CO₂相来产生微孔泡沫。对在SC-CO₂中制备的多孔聚(丙交酯-共-乙交酯)(PLGA)构建体中包封的蛋白质的释放速率进行了体外测量。尽管在最初的48小时内释放了大量蛋白质,但结果表明,使用这种无溶剂技术,蛋白质可能分散在整个聚合物相中并在3周内释放。已知可促进体内血管生成的碱性成纤维细胞生长因子(bFGF)被包封在聚合物基质中。此外,还测量了包封在PLGA泡沫中的bFGF的生物活性保留情况。包封的bFGF在体外从多孔构建体中释放长达10天,生物活性几乎没有损失。

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