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用于生物医学递送应用的纳米结构聚合物整体材料

Nanostructured Polymer Monoliths for Biomedical Delivery Applications.

作者信息

Xie Yihui, Hillmyer Marc A

机构信息

Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455-0431, United States.

出版信息

ACS Appl Bio Mater. 2020 May 18;3(5):3236-3247. doi: 10.1021/acsabm.0c00228. Epub 2020 Apr 21.

Abstract

Drug delivery systems are designed to control the release rate and location of therapeutic agents in the body to achieve enhanced drug efficacy and to mitigate adverse side effects. In particular, drug-releasing implants provide sustained and localized release. We report nanostructured polymer monoliths synthesized by polymerization-induced microphase separation (PIMS) as potential implantable delivery devices. As a model system, free poly(ethylene oxide) homopolymers were incorporated into the nanoscopic poly(ethylene oxide) domains contained within a cross-linked polystyrene matrix. The release of these poly(ethylene oxide) molecules from monoliths was investigated as a function of poly(ethylene oxide) loading and molar mass as well as the molar mass and weight fraction of poly(ethylene oxide) macro-chain transfer agent used in the PIMS process for forming the monoliths. We also developed nanostructured microneedles targeting efficient and long-term transdermal drug delivery by combining PIMS and microfabrication techniques. Finally, given the prominence of poly(lactide) in drug delivery devices, the degradation rate of microphase-separated poly(lactide) in PIMS monoliths was evaluated and compared with bulk poly(lactide).

摘要

药物递送系统旨在控制治疗剂在体内的释放速率和位置,以提高药物疗效并减轻不良副作用。特别是,药物释放植入物可实现持续和局部释放。我们报道了通过聚合诱导微相分离(PIMS)合成的纳米结构聚合物整体材料作为潜在的可植入递送装置。作为模型系统,将游离聚环氧乙烷均聚物掺入交联聚苯乙烯基质中包含的纳米级聚环氧乙烷域中。研究了这些聚环氧乙烷分子从整体材料中的释放情况,作为聚环氧乙烷负载量、摩尔质量以及用于形成整体材料的PIMS过程中使用的聚环氧乙烷大分子链转移剂的摩尔质量和重量分数的函数。我们还通过结合PIMS和微加工技术开发了用于高效和长期透皮给药的纳米结构微针。最后,鉴于聚丙交酯在药物递送装置中的突出地位,评估了PIMS整体材料中微相分离聚丙交酯的降解速率,并与本体聚丙交酯进行了比较。

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