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可注射型弹性蛋白基水凝胶的生物相容性。

Biocompatibility of injectable resilin-based hydrogels.

机构信息

Department of Materials Science and Engineering, University of Delaware, Newark, Delaware, 19716.

Division of Otolaryngology-Head and Neck Surgery, Department of Surgery, University of Wisconsin-Madison, 5136 WIMR, 1111 Highland Ave, Madison, Wisconsin, 53792.

出版信息

J Biomed Mater Res A. 2018 Aug;106(8):2229-2242. doi: 10.1002/jbm.a.36418. Epub 2018 May 11.

DOI:10.1002/jbm.a.36418
PMID:29611890
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6030450/
Abstract

Vocal folds are connective tissues housed in the larynx, which can be subjected to various injuries and traumatic stimuli that lead to aberrant tissue structural alterations and fibrotic-induced biomechanical stiffening observed in patients with voice disorders. Much effort has been devoted to generate soft biomaterials that are injectable directly to sites of injury. To date, materials applied toward these applications have been largely focused on natural extracellular matrix-derived materials such as collagen, fibrin or hyaluronic acid; these approaches have suffered from the fact that materials are not sufficiently robust mechanically nor offer sufficient flexibility to modulate material properties for targeted injection. We have recently developed multiple resilin-inspired elastomeric hydrogels that possess similar mechanical properties as those reported for vocal fold tissues, and that also show promising in vitro cytocompatibility and in vivo biocompatibility. Here we report studies that test the delivery of resilin-based hydrogels through injection to the subcutaneous tissue in a wild-type mice model; histological and genetic expression outcomes were monitored. The rapid kinetics of crosslinking enabled facile injection and ensured the rapid transition of the viscous resilin precursor solution to a solid-like hydrogel in the subcutaneous space in vivo; the materials exhibited storage shear moduli in the range of 1000-2000 Pa when characterized through oscillatory rheology. Histological staining and gene expression profiles suggested minimal inflammatory profiles three weeks after injection, thereby demonstrating the potential suitability for site-specific in vivo injection of these elastomeric materials. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 106A: 2229-2242, 2018.

摘要

声带是位于喉中的结缔组织,可能会受到各种损伤和创伤性刺激,导致声带疾病患者出现异常的组织结构改变和纤维诱导的生物力学僵硬。人们已经投入大量精力来生成可直接注射到损伤部位的软生物材料。迄今为止,应用于这些应用的材料主要集中在天然细胞外基质衍生材料上,如胶原蛋白、纤维蛋白或透明质酸;这些方法存在一个问题,即材料在机械上不够坚固,也没有足够的柔韧性来调节材料特性以进行靶向注射。我们最近开发了多种类弹性蛋白弹性体水凝胶,它们具有与报道的声带组织相似的机械性能,并且在体外细胞相容性和体内生物相容性方面也表现出了良好的效果。在这里,我们报告了通过注射将基于类弹性蛋白的水凝胶递送到野生型小鼠模型的皮下组织的研究;监测了组织学和基因表达结果。交联的快速动力学使得易于注射,并确保粘性类弹性蛋白前体溶液在体内皮下空间中迅速转变为固态水凝胶;通过动态流变学分析,这些材料的存储剪切模量在 1000-2000 Pa 范围内。组织学染色和基因表达谱表明,注射三周后炎症反应最小,从而证明了这些弹性材料在体内特定部位注射的潜在适用性。© 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part A:106A:2229-2242,2018。

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