Urethane-based low-temperature curing, highly-customized and multifunctional poly(glycerol sebacate)-co-poly(ethylene glycol) copolymers

被引:42
|
作者
Wang, Zihao [1 ,3 ]
Ma, Yifan [1 ,3 ]
Wang, YanXiang [1 ,3 ]
Liu, Yutong [1 ,3 ]
Chen, Kai [1 ,3 ]
Wu, Zihan [1 ,3 ]
Yu, Shuang [1 ,3 ]
Yuan, Yuan [1 ,3 ]
Liu, Changsheng [1 ,2 ,3 ]
机构
[1] East China Univ Sci & Technol, Key Lab Ultrafine Mat, Minist Educ, Shanghai 200237, Peoples R China
[2] East China Univ Sci & Technol, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
[3] East China Univ Sci & Technol, Engn Res Ctr Biomat, Minist Educ, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
Supramolecular bioelastomer; Urethane-based PEGylated PGS; Low-temperature curing; Highly-customized; Multiple biomedical applications; IN-VITRO; BIODEGRADABLE ELASTOMERS; BIOMEDICAL APPLICATIONS; POLYURETHANE HYDROGELS; MECHANICAL-PROPERTIES; BONE REGENERATION; SEBACATE); POLYPEPTIDES; SCAFFOLDS; TISSUE;
D O I
10.1016/j.actbio.2018.03.011
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Poly (glycerol sebacate) (PGS), a tough elastomer, has been widely explored in tissue engineering due to the desirable mechanical properties and biocompatibility. However, the complex curing procedure (high temperature and vacuum) and limited hydrophilicity (similar to 90 degrees of wetting angle) greatly impede its functionalities. To address these challenges, a urethane-based low-temperature setting, PEGylated PGS bioelastomer was developed with and without solvent. By simultaneously tailoring PEG and hexamethylene diisocyanate (HDI) contents, the elastomers X-P-mUs (X referred to the PEG content and m referred to HDI content) with a broad ranging mechanical properties and customized hydrophilicity were constructed. The X-P-mUs synthesized exhibited adjustable tensile Young's modulus, ultimate tensile strength and elongation at break in the range of 1.0 MPa-14.2 MPa, 0.3 MPa-7.6 MPa and 53.6%-272.8%, with the water contact angle varying from 28.6 degrees to 71.5 degrees, respectively. Accordingly, these elastomers showed favorable biocompatibility in vitro and mild host response in vivo. Furthermore, the potential applications of X-P-mU elastomers prepared with solvent-base and solvent-free techniques in biomedical fields were investigated. The results showed that these X-P-mU elastomers with high molding capacity at mild temperature could be easily fabricated into various shapes, used as reinforcement for fragile materials, and controllable delivery of drugs and proteins with excellent bioactivity, demonstrating that the X-P-mU elastomers could be tailored as potential building blocks for diverse applications in biomedical research. (C) 2018 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:279 / 292
页数:14
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