A mixture model for water uptake, degradation, erosion and drug release from polydisperse polymeric networks

被引:52
作者
Soares, Joao S. [1 ,2 ]
Zunino, Paolo [1 ]
机构
[1] Politecn Milan, Dept Math F Brioschi, MOX Modeling & Sci Comp, I-20133 Milan, Italy
[2] Univ Tecn Lisboa, Dept Math, CEMAT Ctr Math & Its Applicat, Inst Super Tecn, P-1049001 Lisbon, Portugal
关键词
Modeling; Hydrolysis; Biodegradation; Bioerosion; Controlled drug release; Polylactic acid; BIODEGRADABLE POLYMERS; POLY(LACTIC ACID); ELUTING STENT; MATRICES; TRANSPORT; DELIVERY; PERMEATION; PREDICTION; MOLECULES; KINETICS;
D O I
10.1016/j.biomaterials.2010.01.008
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
We introduce a general class of mixture models suitable to describe water-dependent degradation and erosion of biodegradable polymers in conjunction with drug release. The ability to predict and quantify degradation and erosion has direct impact in a variety of biomedical applications and is a useful design tool for biodegradable implants and tissue engineering scaffolds. The model is based on a finite number of constituents describing the polydisperse polymeric system, each representing chains of an average size, and two additional constituents, water and drug. Hydrolytic degradation of individual chains occurs at the molecular level and mixture constituents diffuse individually accordingly to Fick's 1st law at the bulk level - such analysis confers a multi-scale aspect to the resulting reaction-diffusion system. A shift between two different types of behavior, each identified to surface or bulk erosion, is observed with the variation of a single non-dimensional parameter measuring the relative importance of the mechanisms of reaction and diffusion. Mass loss follows a sigmoid decrease in bulk eroding polymers, whereas decreases linearly in surface eroding polymers. Polydispersity influences degradation and erosion of bulk eroding polymers and drug release from unstable surface eroding matrices is dramatically enhanced in an erosion-controlled release. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3032 / 3042
页数:11
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