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首页> 外文期刊>Journal of biomedical materials research, Part A >Rapid prototyping of three-dimensional nanocomposite hydrogel constructs: Effect of silica nanofiller on swelling and solute release behaviors of the nanocomposite hydrogels
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Rapid prototyping of three-dimensional nanocomposite hydrogel constructs: Effect of silica nanofiller on swelling and solute release behaviors of the nanocomposite hydrogels

机译:三维纳米复合水凝胶结构的快速原型:二氧化硅纳米填料对纳米复合水凝胶溶胀和溶质释放行为的影响

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Three-dimensional (3D) patterning and engineering of biomaterials and biointerfaces have helped bioengineers harness the full potential of cell immobilization for different biomedical applications. However, the bioengineering of an efficient cell immobilized tool, having application in cell biology and tissue engineering, often comes into realization only when a cell friendly immobilization technique is combined with a compatible 3D patterning scheme. We have previously demonstrated the successful blue light induced photopolymerization of poly (ethyleneglycol) diacrylate (PEGDA) based hydrogels for the entrapment of Saccharomyces cerevisiae and NIH 3T3 fibroblast cells. In the present work we have modified rheology of the prepolymer solution by mixing fumed silica nanofiller in different concentrations. Here we demonstrate the rapid prototyping of cell immobilized nanocomposite hydrogels, where S. cerevisiae loaded nanofilled prepolymer solution was directly written in layer-by-layer fashion using solid free form fabrication also known as rapid prototyping technique and was cross-linked into 3D cell loaded construct via blue light induced polymerization. The swelling trend was found to be a function of silica nanofiller concentration and transitioned from decreasing to increasing type at 10% w/v nanofiller concentration. Dynamic swelling profile predicted that the swelling agent transported with in the gels via super case II type transport mechanism irrespective of the crosslink density. In contrast, the mode of transportation of the loaded solute was found to be fickian and nonfickian type respectively for loosely and tightly crosslinked gels. Spatial heterogeneity in the crosslinked network was resulted upon blue light curing, subsequently the 3D growth of the immobilized cells was observed to be a function of crosslink density. (c) 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 3237-3249, 2015.
机译:生物材料和生物界面的三维(3D)图案化和工程化已经帮助生物工程师利用细胞固定化的全部潜力来满足不同的生物医学应用。但是,只有将细胞友好的固定技术与兼容的3D图案化方案结合起来,才能在细胞生物学和组织工程中应用有效的细胞固定工具,进行生物工程改造。先前我们已经证明了成功的蓝光诱导的聚(乙二醇)二丙烯酸酯(PEGDA)基水凝胶的光致聚合,可用于酿酒酵母和NIH 3T3成纤维细胞的包裹。在目前的工作中,我们通过混合不同浓度的气相二氧化硅纳米填料,改变了预聚物溶液的流变性。在这里,我们展示了固定化细胞的纳米复合水凝胶的快速原型,其中酿酒酵母加载的纳米填充预聚物溶液是使用无固体形式的制造(也称为快速原型化技术)以逐层方式直接编写的,并交联到加载3D细胞中通过蓝光诱导的聚合反应构建。发现溶胀趋势是二氧化硅纳米填料浓度的函数,并且在10%w / v纳米填料浓度时从减少型转变为增加型。动态溶胀曲线预测溶胀剂通过super case II型转运机制在凝胶中转运,而与交联密度无关。相反,对于松散和紧密交联的凝胶,发现负载的溶质的运输方式分别为菲克式和非菲克式。蓝光固化导致了交联网络中的空间异质性,随后观察到固定化细胞的3D生长是交联密度的函数。 (c)2015 Wiley Periodicals,Inc. J Biomed Mater Res Part A:103A:3237-3249,2015年。

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