Self-Healing Elastin-Bioglass Hydrogels

被引:54
作者
Zeng, Qiongyu [1 ,2 ,3 ]
Desai, Malay S. [1 ,2 ]
Jin, Hyo-Eon [1 ,2 ,5 ]
Lee, Ju Hun [1 ,2 ]
Chang, Jiang [3 ,4 ]
Lee, Seung-Wuk [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[2] Lawrence Berkeley Natl Lab, Biol Syst & Engn Div, Berkeley, CA 94720 USA
[3] Shanghai Jiao Tong Univ, Med X Res Inst, Sch Biomed Engn, 1954 Huashan Rd, Shanghai 200030, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Ceram, 1295 Dingxi Rd, Shanghai 200050, Peoples R China
[5] Ajou Univ, Coll Pharm, Suwon 16499, South Korea
关键词
BIOACTIVE GLASS; DRUG-DELIVERY; COMPOSITE HYDROGEL; BIOMEDICAL APPLICATIONS; INJECTABLE HYDROGELS; CELL CARRIERS; CROSS-LINKING; POLYPEPTIDES; POLYMERS; PROTEIN;
D O I
10.1021/acs.biomac.6b00621
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tailorable hydrogels that are mechanically robust, injectable, and self-healable, are useful for many biomedical applications including tissue repair and drug delivery. Here we use biological and chemical engineering approaches to develop a novel in situ forming organic/ inorganic composite hydrogel with dynamic aldimine cross links using elastin-like polypeptides (ELP) and bioglass (BG). The resulting ELP/BG biocomposites exhibit tunable gelling behavior and mechanical characteristics in a composition and concentration dependent manner. We also demonstrate self-healing in the ELP/BG hydrogels by successfully reattaching severed pieces as well as through rheology. In addition, we show the strength of genetic engineering to easily customize ELP by fusing cell-stimulating "RGD" peptide motifs. We showed that the resulting composite materials are cytocompatible as they support the cellular growth and attachment. Our robust in situ forming ELP/BG composite hydrogels will be useful as injectable scaffolds for delivering cell and drug molecules to promote soft tissue regeneration in the future.
引用
收藏
页码:2619 / 2625
页数:7
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