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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.
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页码:2619 / 2625
页数:7
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