Development of an Injectable Nitric Oxide Releasing Poly(ethylene) Glycol-Fibrin Adhesive Hydrogel

被引:36
作者
Joseph, Carly A. [1 ]
McCarthy, Connor W. [1 ]
Tyo, Ariana G. [1 ]
Hubbard, Kenneth R. [1 ]
Fisher, Hannah C. [1 ]
Altscheffel, Jacob A. [1 ]
He, Weilue [1 ]
Pinnaratip, Rattapol [1 ]
Liu, Yuan [1 ]
Lee, Bruce P. [1 ]
Rajachar, Rupak M. [1 ]
机构
[1] Michigan Technol Univ, Dept Biomed Engn, 1400 Townsend Dr, Houghton, MI 49931 USA
来源
ACS BIOMATERIALS SCIENCE & ENGINEERING | 2019年 / 5卷 / 02期
基金
美国国家卫生研究院;
关键词
fibrin hydrogel; inducible; injectable; microparticle; nitric oxide; PEG-NHS; TISSUE ADHESIVE; CHEMISTRY; BIOMATERIALS; EFFICACY; CELLS; NO;
D O I
10.1021/acsbiomaterials.8b01331
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Fibrin microparticles were incorporated into poly(ethylene) glycol (PEG)-fibrinogen hydrogels to create an injectable composite that could serve as a wound healing support and vehicle to deliver therapeutic factors for tissue engineering. Nitric oxide (NO), a therapeutic agent in wound healing, was loaded into fibrin microparticles by blending S-nitroso-N-acetyl penicillamine (SNAP) with a fibrinogen solution. The incorporation of microparticles affected swelling behavior and improved tissue adhesivity of composite hydrogels. Controlled NO release was induced via photolytic and thermal activation, and modulated by weight percent of particles incorporated. These NO-releasing composites were noncytotoxic in culture. Cells maintained morphology, viability, and proliferative character. Fibrin microparticles loaded with SNAP and incorporated into a PEG-fibrinogen matrix creates a novel injectable composite hydrogel that offers improved tissue adhesivity and inducible NO-release for use as a regenerative support for wound healing and tissue engineering applications.
引用
收藏
页码:959 / 969
页数:21
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