Mechanical characterization of sequentially layered photo-clickable thiol-ene hydrogels

被引:20
|
作者
Aziz, Aaron H. [1 ,2 ]
Wahlquist, Joseph [3 ]
Soliner, Aaron [1 ]
Ferguson, Virginia [2 ,3 ,5 ]
DelRio, Frank W. [4 ]
Bryant, Stephanie J. [1 ,2 ,5 ]
机构
[1] Univ Colorado, Dept Chem & Biol Engn, UCB 596,3415 Colorado Ave, Boulder, CO 80309 USA
[2] Univ Colorado, BioFrontiers Inst, Boulder, CO 80309 USA
[3] Univ Colorado, Dept Mech Engn, Boulder, CO 80309 USA
[4] NIST, Appl Chem & Mat Div, Mat Measurement Lab, Boulder, CO 80305 USA
[5] Univ Colorado, Mat Sci & Engn Program, Boulder, CO 80309 USA
基金
美国国家科学基金会;
关键词
Multi-layer hydrogel; Interfacial properties; Nanoindentation; Atomic force microscopy; RADICAL POLYMERIZATION KINETICS; SOLUTE DIFFUSION; MULTILAYER HYDROGEL; ARTICULAR-CARTILAGE; PRIMARY CYCLIZATION; PEG HYDROGELS; SCAFFOLD; GLYCOL); GELS; DIFFERENTIATION;
D O I
10.1016/j.jmbbm.2016.09.007
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Multi-layer hydrogels are promising for tissue engineering due to the ability to control the local properties within each layer. However, the interface that forms between each layer-has the potential to affect the performance of the hydrogel. The goals of this study were to characterize how the interface forms via its thickness and mechanical properties, identify its impact on the overall hydrogel properties, and provide new insights into how to control the interface. A photo-clickable poly(ethylene glycol) hydrogel was used to form bilayer hydrogels that were sequentially polymerized in a step-and-repeat process. Different processing conditions were studied: the time (0-20 min) before initiating polymerization of the second layer (soak time, t(s)) and the hydrogel crosslink density (the same, less crosslinked, or more crosslinked) of the first layer as compared to the second layer. Interface thickness was characterized by confocal microscopy, monomer transport by Fickian diffusion, single and bilayer hydrogel mechanics by bulk moduli measurements, and interface moduli measurements using AFM, nanoindentation, and strain mapping. The interface thickness ranged from similar to 70 to 600 lam (1-10% of total height) depending on processing conditions, but did not affect the bulk hydrogel modulus. Analysis of monomer transport revealed that convection, due to changes in hydrogel swelling, and diffusion contribute to interface thickness. Nanomechanical analysis of bilayer hydrogels formed from soft (75 kPa) and stiff (250 kPa) layers showed a gradient in elastic modulus across the interface, which corresponded to strain maps. In summary, this work identifies that diffusive and convective transport of monomers across the interface controls its thickness and that a mechanically robust interface forms, which does.not affect the hydrogel modulus. By controlling the processing conditions, the thickness of the interface can be tuned without affecting the mechanical properties of the bulk hydrogel. (C) 2004 Published by Elsevier Ltd.
引用
收藏
页码:454 / 465
页数:12
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