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通过形成溶菌酶-油酸盐复合物,将溶菌酶从电纺聚(ε-己内酯)/聚(乙二醇)非织造膜中包封和控制释放。

Encapsulation and controlled release of lysozyme from electrospun poly(epsilon-caprolactone)/poly(ethylene glycol) non-woven membranes by formation of lysozyme-oleate complexes.

作者信息

Li Yan, Jiang Hongliang, Zhu Kangjie

机构信息

Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, China.

出版信息

J Mater Sci Mater Med. 2008 Feb;19(2):827-32. doi: 10.1007/s10856-007-3175-6. Epub 2007 Jul 31.

Abstract

In this study, the concept of hydrophobic ion pairing was adopted for incorporating lysozyme into electrospun poly(epsilon-caprolactone) (PCL)/poly(ethylene glycol) (PEG) non-woven membranes. The solubility of lysozyme in organic solvent was enhanced through the formation of lysozyme-oleate complexes, which could be directly loaded into PCL/PEG membranes using electrospinning technique. The resultant PCL/PEG nanofibers have a compact structure with an average diameter ranged from about 0.4 microm to 0.9 microm. The addition of PEG into the PCL nanofibers not only improved the hydrophilicity of the membrane, but also played an important role on in vitro lysozyme release rate. It was found that the release rate of lysozyme was enhanced with the increase of PEG content. In addition, the increase of salt concentration in the release medium accelerated lysozyme release. It has also been shown that the released lysozyme retained most of its enzymatic activity.

摘要

在本研究中,采用疏水离子对的概念将溶菌酶掺入静电纺聚己内酯(PCL)/聚乙二醇(PEG)非织造膜中。通过形成溶菌酶 - 油酸酯复合物提高了溶菌酶在有机溶剂中的溶解度,该复合物可使用静电纺丝技术直接载入PCL/PEG膜中。所得的PCL/PEG纳米纤维具有紧密结构,平均直径范围约为0.4微米至0.9微米。在PCL纳米纤维中添加PEG不仅改善了膜的亲水性,而且对体外溶菌酶释放速率也起重要作用。发现随着PEG含量的增加,溶菌酶的释放速率提高。此外,释放介质中盐浓度的增加加速了溶菌酶的释放。还表明,释放的溶菌酶保留了其大部分酶活性。

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