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首页> 外文期刊>European journal of pharmaceutical sciences >Delivery of bioactive macromolecules from microporous polymer matrices: Release and activity profiles of lysozyme, collagenase and catalase.
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Delivery of bioactive macromolecules from microporous polymer matrices: Release and activity profiles of lysozyme, collagenase and catalase.

机译:从微孔聚合物基质中递送生物活性大分子:溶菌酶,胶原酶和过氧化氢酶的释放和活性曲线。

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摘要

Microporous polycaprolactone (PCL) matrices containing lysozyme, collagenase and catalase respectively with molecular weight covering a wide range from 14.3 to 240kDa were produced by a novel method involving rapid cooling of particle suspensions in dry ice. The enzyme loading efficiency (lysozyme (50%), collagenase (75%) and catalase (90%)) depended on the enzyme molecular weight and the non-solvent used to extract acetone from the hardened matrices. Sustained enzyme release occurred from the PCL matrices over 11 days with retained activity dependent on the particular enzyme used (collagenase 100% activity at 11 days, lysozyme 75-80% at 11 days, catalase 10-20% at 5 days). The present findings confirm the potential of microporous PCL matrices for delivering bioactive macromolecules from implantable/insertable depot-type formulations and tissue engineering scaffolds and recommend catalase as a challenging model protein for evaluating such devices.
机译:通过一种新颖的方法制备含溶菌酶,胶原酶和过氧化氢酶的微孔聚己内酯(PCL)基质,分子量分别覆盖14.3至240kDa的宽范围,该方法涉及在干冰中快速冷却颗粒悬浮液。酶的负载效率(溶菌酶(50%),胶原酶(75%)和过氧化氢酶(90%))取决于酶的分子量和从硬化基质中提取丙酮所用的非溶剂。从PCL基质持续释放酶超过11天,保留的活性取决于所使用的特定酶(胶原酶在11天时为100%活性,溶菌酶在11天时为75-80%,过氧化氢酶在5天时为10-20%)。目前的发现证实了微孔PCL基质从可植入/可插入的长效型制剂和组织工程支架中递送生物活性大分子的潜力,并推荐过氧化氢酶作为一种具有挑战性的模型蛋白来评估此类设备。

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