Mechanical characterization and non-linear elastic modeling of poly(glycerol sebacate) for soft tissue engineering

被引:37
作者
Mitsak, Anna G. [1 ]
Dunn, Andrew M. [1 ]
Hollister, Scott J. [1 ,2 ,3 ]
机构
[1] Dept Biomed Engn, Ann Arbor, MI 48104 USA
[2] Univ Michigan, Dept Mech Engn, GG Brown Lab, Ann Arbor, MI 48109 USA
[3] Dept Surg, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会;
关键词
Poly(glycerol sebacate); Tissue engineering; Neo-Hookean; IN-VITRO; HYALURONIC-ACID; CHITOSAN SCAFFOLDS; HEART-MUSCLE; COLLAGEN; FIBRIN; PROLIFERATION; BIOCOMPATIBILITY; DIFFERENTIATION; DEFORMATION;
D O I
10.1016/j.jmbbm.2011.11.003
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Scaffold tissue engineering strategies for repairing and replacing soft tissue aim to improve reconstructive and corrective surgical techniques whose limitations include suboptimal mechanical properties, fibrous capsule formation and volume loss due to graft resorption. An effective tissue engineering strategy requires a scaffolding material with low elastic modulus that behaves similarly to soft tissue, which has been characterized as a nonlinear elastic material. The material must also have the ability to be manufactured into specifically designed architectures. Poly(glycerol sebacate) (PGS) is a thermoset elastomer that meets these criteria. We hypothesize that the mechanical properties of PGS can be modulated through curing condition and architecture to produce materials with a range of stiffnesses. To evaluate this hypothesis, we manufactured PGS constructs cured under various conditions and having one of two architectures (solid or porous). Specimens were then tensile tested according to ASTM standards and the data were modeled using a nonlinear elastic Neo-Hookean model. Architecture and testing conditions, including elongation rate and wet versus dry conditions, affected the mechanical properties. Increasing curing time and temperature led to increased tangent modulus and decreased maximum strain for solid constructs. Porous constructs had lower nonlinear elastic properties, as did constructs of both architectures tested under simulated physiological conditions (wetted at 37 degrees C). Both solid and porous PGS specimens could be modeled well with the Neo-Hookean model. Future studies include comparing PGS properties to other biological tissue types and designing and characterizing PGS scaffolds for regenerating these tissues. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3 / 15
页数:13
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