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聚乙交酯:降解与药物释放。第二部分:药物释放。

Polyglycolide: degradation and drug release. Part II: drug release.

作者信息

Hurrell S, Cameron R E

机构信息

Department of Materials Science and Metallurgy, University of Cambridge, Pembroke Street, Cambridge, CB2 3QZ.

出版信息

J Mater Sci Mater Med. 2001 Sep;12(9):817-20. doi: 10.1023/a:1017910408871.

Abstract

This paper considers drug release from a polyglycolide (PGA) matrix and is divided into two sections. The first investigates the effects on the degradation of the polymer of incorporating a model drug, theophylline, into the polymer. Small and wide angle X-ray scattering, and mass loss and water uptake measurements indicate that the presence of this drug does not affect the time scale of the degradation process. However, the dissolved theophylline molecules affect the extent to which the polymer crystallizes during degradation. In the second section, theophylline release profiles, obtained using UV-spectrophotometry, show that the erosion of the polymer controls the release of the drug. The drug release results add further evidence to support the four stage degradation process which was described in Part I.

摘要

本文研究了聚乙交酯(PGA)基质中的药物释放情况,分为两个部分。第一部分研究了将模型药物茶碱掺入聚合物中对聚合物降解的影响。小角和广角X射线散射、质量损失和吸水率测量表明,这种药物的存在不会影响降解过程的时间尺度。然而,溶解的茶碱分子会影响聚合物在降解过程中的结晶程度。在第二部分中,使用紫外分光光度法获得的茶碱释放曲线表明,聚合物的侵蚀控制着药物的释放。药物释放结果进一步证明了第一部分中描述的四阶段降解过程。

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