Mathematical modeling of degradation for bulk-erosive polymers: Applications in tissue engineering scaffolds and drug delivery systems

被引:133
作者
Chen, Yuhang [1 ]
Zhou, Shiwei [1 ]
Li, Qing [1 ]
机构
[1] Univ Sydney, Sch Aerosp Mech & Mechatron Engn, Sydney, NSW 2006, Australia
基金
澳大利亚研究理事会;
关键词
Biodegradation; Biodegradable polymers; Autocatalysis; Microparticle; Scaffold; COMPUTER-AIDED-DESIGN; PLGA MICROSPHERES; HYDROLYTIC DEGRADATION; BIODEGRADABLE POLYMERS; CONTROLLED-RELEASE; BONE REGENERATION; MICROCLIMATE PH; FINITE-ELEMENT; IN-VITRO; DEVICES;
D O I
10.1016/j.actbio.2010.09.038
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
The degradation of polymeric biomaterials, which are widely exploited in tissue engineering and drug delivery systems, has drawn significant attention in recent years. This paper aims to develop a mathematical model that combines stochastic hydrolysis and mass transport to simulate the polymeric degradation and erosion process. The hydrolysis reaction is modeled in a discrete fashion by a fundamental stochastic process and an additional autocatalytic effect induced by the local carboxylic acid concentration in terms of the continuous diffusion equation. Illustrative examples of microparticles and tissue scaffolds demonstrate the applicability of the model. It is found that diffusive transport plays a critical role in determining the degradation pathway, whilst autocatalysis makes the degradation size dependent. The modeling results show good agreement with experimental data in the literature, in which the hydrolysis rate, polymer architecture and matrix size actually work together to determine the characteristics of the degradation and erosion processes of bulk-erosive polymer devices. The proposed degradation model exhibits great potential for the design optimization of drug carriers and tissue scaffolds. (C) 2010 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1140 / 1149
页数:10
相关论文
共 54 条
[1]
Framework for optimal design of porous scaffold microstructure by computational simulation of bone regeneration [J].
Adachi, T ;
Osako, Y ;
Tanaka, M ;
Hojo, M ;
Hollister, SJ .
BIOMATERIALS, 2006, 27 (21) :3964-3972
[2]
Effects of fluid flow on the in vitro degradation kinetics of biodegradable scaffolds for tissue engineering [J].
Agrawal, CM ;
McKinney, JS ;
Lanctot, D ;
Athanasiou, KA .
BIOMATERIALS, 2000, 21 (23) :2443-2452
[3]
Amass W, 1998, POLYM INT, V47, P89, DOI 10.1002/(SICI)1097-0126(1998100)47:2<89::AID-PI86>3.0.CO
[4]
2-F
[5]
Biodegradation and biocompatibility of PLA and PLGA microspheres [J].
Anderson, JM ;
Shive, MS .
ADVANCED DRUG DELIVERY REVIEWS, 1997, 28 (01) :5-24
[6]
Mathematical modeling and simulation of drug release from microspheres: Implications to drug delivery systems [J].
Arifin, Davis Yohanes ;
Lee, Lai Yeng ;
Wang, Chi-Hwa .
ADVANCED DRUG DELIVERY REVIEWS, 2006, 58 (12-13) :1274-1325
[7]
Extracellular matrix as a biological scaffold material: Structure and function [J].
Badylak, Stephen F. ;
Freytes, Donald O. ;
Gilbert, Thomas W. .
ACTA BIOMATERIALIA, 2009, 5 (01) :1-13
[8]
Quantitative multi-agent models for simulating protein release from PLGA bioerodible nano- and microspheres [J].
Barat, Ana ;
Crane, Martin ;
Ruskin, Heather J. .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2008, 48 (02) :361-368
[9]
Modeling drug release from bioerodible microspheres using a cellular automaton [J].
Bertrand, Nicolas ;
Leclair, Gregoire ;
Hildgen, Patrice .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2007, 343 (1-2) :196-207
[10]
Hydrolytic degradation and drug release properties of ganciclovir-loaded biodegradable microspheres [J].
Chen, Xi ;
Ooi, Chui Ping .
ACTA BIOMATERIALIA, 2008, 4 (04) :1046-1056