PDMSstar-PEG hydrogels prepared via solvent-induced phase separation (SIPS) and their potential utility as tissue engineering scaffolds

被引:30
作者
Bailey, Brennan M. [1 ,2 ]
Fei, Ruochong [1 ]
Munoz-Pinto, Dany [3 ]
Hahn, Mariah S. [2 ,3 ]
Grunlan, Melissa A. [1 ,2 ]
机构
[1] Texas A&M Univ, Dept Biomed Engn, College Stn, TX 77843 USA
[2] Texas A&M Univ, Mat Sci & Engn Program, College Stn, TX 77843 USA
[3] Texas A&M Univ, Dept Chem Engn, College Stn, TX 77843 USA
关键词
Poly(ethylene glycol); Polydimethylsiloxane; Hydrogel; Scaffold; Tissue engineering; POLY(ETHYLENE GLYCOL)-BASED HYDROGELS; IN-VITRO DEGRADATION; SMOOTH-MUSCLE-CELLS; EXTRACELLULAR-MATRIX; POLYMERIC BIOMATERIALS; MECHANICAL-PROPERTIES; GELATIN-SILOXANE; ASPECT-RATIO; MESH SIZE; BEHAVIOR;
D O I
10.1016/j.actbio.2012.07.034
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Inorganic-organic hydrogels based on methacrylated star polydimethylsiloxane (PDMSstar-MA) and diacrylated poly(ethylene glycol) (PEG-DA) macromers were prepared via solvent-induced phase separation (SIPS). The macromers were combined in a dichloromethane precursor solution and sequentially photopolymerized, dried and hydrated. The chemical and physical properties of the hydrogels were further tailored by varying the number average molecular weight (M-n) of PEG-DA (M-n = 3.4k and 6k g mol(-1)) as well as the weight percent ratio of PDMSstar-MA (M-n = 7k g mol(-1)) to PEG-DA from 0:100 to 20:80. Compared to analogous hydrogels fabricated from aqueous precursor solutions, SIPS produced hydrogels with a macroporous morphology, a more even distribution of PDMS(star)MA, increased modulus and enhanced degradation rates. The morphology, swelling ratio, mechanical properties, bioactivity, non-specific protein adhesion, controlled introduction of cell adhesion, and cytocompatibility of the hydrogels were characterized. As a result of their tunable properties, this library of hydrogels is useful to study materialguided cell behavior and ultimate tissue regeneration. (C) 2012 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:4324 / 4333
页数:10
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