三螺旋
生物材料
材料科学
胶原螺旋
共价键
纺纱
复合材料
化学
极限抗拉强度
高分子化学
纳米技术
有机化学
立体化学
作者
M. Tarik Arafat,Giuseppe Tronci,Jie Yin,David J. Wood,Stephen J. Russell
出处
期刊:Polymer
[Elsevier]
日期:2015-09-19
卷期号:77: 102-112
被引量:56
标识
DOI:10.1016/j.polymer.2015.09.037
摘要
One of the limitations of electrospun collagen as bone-like fibrous structure is the potential collagen triple helix denaturation in the fibre state and the corresponding inadequate wet stability even after crosslinking. Here, we have demonstrated the feasibility of accomplishing wet-stable fibres by wet spinning and diacid-based crosslinking of collagen triple helices, whereby fibre ability to act as bone-mimicking mineralisation system has also been explored. Circular dichroism (CD) demonstrated nearly complete triple helix retention in resulting wet-spun fibres, and the corresponding chemically crosslinked fibres successfully preserved their fibrous morphology following 1-week incubation in phosphate buffer solution (PBS). The presented novel diacid-based crosslinking route imparted superior tensile modulus and strength to the resulting fibres indicating that covalent functionalization of distant collagen molecules is unlikely to be accomplished by current state-of-the-art carbodiimide-based crosslinking. To mimic the constituents of natural bone extra cellular matrix (ECM), the crosslinked fibres were coated with carbonated hydroxyapatite (CHA) through biomimetic precipitation, resulting in an attractive biomaterial for guided bone regeneration (GBR), e.g. in bony defects of the maxillofacial region.
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