Mechanical study of PLA-PCL fibers during in vitro degradation

被引:210
作者
Vieira, A. C. [1 ,2 ]
Vieira, J. C. [1 ]
Ferra, J. M. [3 ]
Magalhaes, F. D. [3 ]
Guedes, R. M. [2 ]
Marques, A. T. [2 ]
机构
[1] Inst Mech Engn & Ind Management, UMEC, P-4200465 Oporto, Portugal
[2] Univ Porto, Fac Engn, Dept Mech Engn, DEMec, P-4200465 Oporto, Portugal
[3] Univ Porto, Fac Engn, LEPAE Chem Engn Dept, P-4200465 Oporto, Portugal
关键词
PLA-PCL properties; Hydrolysis; Degradation; Modeling; HYDROLYTIC DEGRADATION; BIODEGRADABLE POLYMERS; ENZYMATIC DEGRADATION; MOLECULAR-WEIGHT; DRUG-RELEASE; POLY(L-LACTIDE); BLENDS; MODEL; ACID); CRYSTALLIZATION;
D O I
10.1016/j.jmbbm.2010.12.006
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The aliphatic polyesters are widely used in biomedical applications since they are susceptible to hydrolytic and/or enzymatic chain cleavage, leading to alpha-hydroxyacids, generally metabolized in the human body. This is particularly useful for many biomedical applications, especially, for temporary mechanical supports in regenerative medical devices. Ideally, the degradation should be compatible with the tissue recovering. In this work, the evolution of mechanical properties during degradation is discussed based on experimental data. The decrease of tensile strength of PLA-PCL fibers follows the same trend as the decrease of molecular weight, and so it can also be modeled using a first order equation. For each degradation stage, hyperelastic models such as Neo-Hookean, Mooney-Rivlin and second reduced order, allow a reasonable approximation of the material behavior. Based on this knowledge, constitutive models that describe the mechanical behavior during degradation are proposed and experimentally validated. The proposed theoretical models and methods may be adapted and used in other biodegradable materials, and can be considered fundamental tools in the design of regenerative medical devices where strain energy is an important requirement, such as, for example, ligaments, cartilage and stents. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:451 / 460
页数:10
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