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含多嵌段共聚物的聚(ε-己内酯)的选择性酶促降解

Selective enzymatic degradation of poly(epsilon-caprolactone) containing multiblock copolymers.

作者信息

Kulkarni A, Reiche J, Hartmann J, Kratz K, Lendlein A

机构信息

Experimental Physics, University of Potsdam, Potsdam, Germany.

出版信息

Eur J Pharm Biopharm. 2008 Jan;68(1):46-56. doi: 10.1016/j.ejpb.2007.05.021. Epub 2007 Jul 14.

Abstract

The hydrolytic and Pseudomonas lipase catalysed enzymatic degradation was studied for PDC multiblock copolymers consisting of poly(epsilon-caprolactone) (PCL) segments and poly(p-dioxanone) (PPDO) segments with variable composition. The enzymatic degradation of these multiblock copolymers is significantly accelerated by Pseudomonas lipase in contrast to the hydrolytic degradation where the degradation behaviour is determined by the PPDO segments. Degradation time intervals up to 200h are selected, where the PPDO segments remain stable and do not contribute to the degradation process. A linear correlation between weight loss and increasing PCL content of the multiblock copolymers was found. X-ray diffraction data confirm that both crystalline and amorphous PCL are attacked by the enzymes. SEM cross-section images reveal that Pseudomonas lipase penetrates into the PDC polymers. The present study impressively demonstrates that selective enzymatic degradation of PCL containing multifunctional polymers is a beneficial tool for controlling their degradation properties.

摘要

研究了由聚(ε-己内酯)(PCL)链段和聚(对二氧环己酮)(PPDO)链段组成的不同组成的聚己内酯-聚对二氧环己酮多嵌段共聚物(PDC)的水解降解和假单胞菌脂肪酶催化的酶促降解。与水解降解相比,这些多嵌段共聚物的酶促降解在假单胞菌脂肪酶的作用下显著加速,水解降解行为由PPDO链段决定。选择了长达200小时的降解时间间隔,在此期间PPDO链段保持稳定,不参与降解过程。发现多嵌段共聚物的重量损失与PCL含量增加之间存在线性关系。X射线衍射数据证实,结晶和无定形PCL均受到酶的攻击。扫描电子显微镜横截面图像显示,假单胞菌脂肪酶可渗透到PDC聚合物中。本研究令人印象深刻地表明,含PCL的多功能聚合物的选择性酶促降解是控制其降解性能的有益工具。

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