Thermoresponsive nanocomposite hydrogels with cell-releasing behavior

被引:100
作者
Hou, Yaping [1 ]
Matthews, Andrew R. [1 ]
Smitherman, Ashley M. [1 ]
Bulick, Allen. S. [2 ]
Hahn, Mariah S. [2 ]
Hou, Huijie [3 ]
Han, Arum [3 ]
Grunlan, Melissa A. [1 ]
机构
[1] Texas A&M Univ, Dept Biomed Engn, College Stn, TX 77843 USA
[2] Texas A&M Univ, Dept Chem Engn, College Stn, TX 77843 USA
[3] Texas A&M Univ, Dept Elect & Comp Engn, College Stn, TX 77843 USA
基金
美国国家科学基金会;
关键词
hydrogel; thermally responsive material; siloxane; nanoparticles; cell adhesion; photopolymerization;
D O I
10.1016/j.biomaterials.2008.04.024
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Poly(N-isopropylacrylamide) (PNIPAAm) hydrogels become more hydrophobic when they reversibly switch from a water-swollen to a deswollen state above the volume phase transition temperature (VPTT, similar to 33 degrees C) which has been used to modulate cell adhesion. In the current work, we prepared novel thermoresponsive nanocomposite hydrogels comprised of a PNIPAAm hydrogel matrix and polysiloxane colloidal nanoparticles (similar to 220 nm average diameter) via in situ photopolymerization of aqueous solutions of NIPAAm monomer, N,N'-methylenebisacrylamide (BIS, crosslinker), photoinitiator and polysiloxane nanoparticles (0.5-2.0 wt% based on solution weight) at similar to 7 degrees C. The VPTT of the nanocomposite hydrogels is not altered versus the pure PNIPAAm hydrogel. Dynamic mechanical analysis and tensile tests revealed that higher nanoparticle content generally produced improved hydrogel mechanical properties. Surfaces of nanocomposite hydrogels became increasingly more hydrophobic at all temperatures between 10 and 40 degrees C as the amount of hydrophobic polysiloxane nanoparticles was increased. When cooled from 37 to 25 degrees C, mouse smooth muscle precursor cells (10T1/2) were effectively detached from nanocomposite hydrogel surfaces. The utility of photopatterning to create surface micropillars comprised of nanocomposite hydrogels was demonstrated. Published by Elsevier Ltd.
引用
收藏
页码:3175 / 3184
页数:10
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