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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >An efficient two-step preparation of photocrosslinked gelatin microspheres as cell carriers to support MC3T3-E1 cells osteogenic performance
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An efficient two-step preparation of photocrosslinked gelatin microspheres as cell carriers to support MC3T3-E1 cells osteogenic performance

机译:光源瘤明胶微球作为细胞载体的高效两步制备,以支持MC3T3-E1细胞骨质发生性能

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摘要

Gelatin microspheres have been commonly used in tissue engineering, but their application is often limited by the uncontrollability and potential cytotoxicity of traditional chemical cross-linking method. Methylacrylamide modification and photocrosslinking provide a controllable and cytocompatible cross-linking method for gelatin hydrogels, however, microspheres fabricated by this single photopolymerization process is uncontrollable. In this study, we show that increasing the gelling ability of gelatin methacrylamide (GMA) at low temperatures is vital to prepare photocrosslinked gelatin microspheres, which in turn improves the controllability and compatibility of conventional chemical cross-linking methods. We detailed characterized the rheological performance with varying temperature and demonstrated that the gelling capability of GMA could be improved by increasing GMA solution concentration and reducing methacrylate substitution. The physicochemical properties of the photocrosslinked microspheres can be modulated via methacrylamide modification, as evidenced by the positive correlation between the physicochemical optimization of the hydrogel bulk and the degree of methacrylate substitution. Next, we successfully fabricated GMA spheres by a two-step process of low-temperature gelation followed by photopolymerization crosslinking. Finally, we show that the microcarriers exhibited favorable supporting for MC3T3-E1 cell proliferation, spreading, and osteogenic differentiation. This study provided a controllable and cytocompatible photocrosslinking procedure for GMA microspheres with broad application prospects, of course, not limited to cell microcarriers.
机译:明胶微球已经常用于组织工程,但它们的应用通常受传统化学交联方法的不可控制和潜在的细胞毒性的限制。甲基丙烯酰胺改性和光学源分解提供了明胶水凝胶的可控和细胞势互相相干的交联方法,然而,通过该单一光聚合过程制造的微球是无法控制的。在这项研究中,我们表明,在低温下增加明胶甲基丙烯酰胺(GMA)的胶凝能力对于制备光学表带的明胶微球至关重要,这又改善了常规化学交联方法的可控性和相容性。我们详细用来具有不同温度的流变性能,并证明通过增加GMA溶液浓度并降低甲基丙烯酸酯取代,可以提高GMA的胶凝能力。光源源细胞的物理化学性能可以通过甲基丙烯酰胺改性调节,如水凝胶块状物理化学优化与甲基丙烯酸酯取代度之间的正相关性所证明。接下来,我们通过两步工艺通过低温凝胶化的两步工艺成功地制造了GMA球体,然后通过光聚合交联。最后,我们表明微载体表现出对MC3T3-E1细胞增殖,扩散和成骨分化的良好支持。该研究提供了具有广泛应用前景的GMA微球的可控和细胞势不可平相的光电解过程,当然不限于细胞微载体。

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