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Evaluation of Biological Responses of UMR-106 Cells to Porous PHBV Matrix

机译:UMR-106细胞对多孔PHBV矩阵的生物反应评价

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This paper compared the results of osteoblast-like UMR-106 cells response to 3-D biodegradable porous with nonporous PHBV (poly (3-hydroxybutyrate-co-3-hydroxyvalerate) films. Nonporous PHBV films were prepared by solvent casting and evaporation. Porous PHBV films were prepared by solute leaching of salt/PHBV cast film. Sieved sodium chloride (~150μm) was used to create a matrix with high porosity and then leached out by the solvent. Thermo gravimetric analysis showed that over 99% of the salts were leached out by the solvent. Osteoblast-like UMR-106 cells were seeded onto the nonporous and porous PHBV films, respectively. After 6 and 10 days of incubation, the growth rate of UMR-106 cells on porous film was higher than on nonporous film. Viable cell proliferation on the porous and nonporous PHBV film was quantified by (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt) (MTS) assay. The results of this study suggest that UMR-106 cells proliferate more on the porous PHBV matrix and porous PHBV films are a promising material for bone tissue engineering applications.
机译:本文将成骨细胞样UMR-106细胞的结果与无孔PHBV(聚(3-羟基丁酸酯-CO-3-羟基戊羟戊苯基)膜进行了3D可生物降解多孔的响应。通过溶剂浇铸和蒸发制备无孔PHBV薄膜。多孔通过溶质浸出盐/ pHBV浇铸薄膜制备PHBV薄膜。使用氯化钠(〜150μm)来制备具有高孔隙率的基质,然后通过溶剂浸出。热重量分析显示,超过99%的盐用溶剂浸出。分别将成骨细胞样UMR-106细胞接种到无孔和多孔的PHBV膜上。孵育6至10天后,多孔膜上的UMR-106细胞的生长速率高于无孔膜。通过(3-(4,5-二甲基噻唑-2-基)-5-(3-羧甲氧基苯基)-2-(4-磺酰苯基)-2H-四唑,内部的可行细胞增殖(3-(4,5-二甲基噻唑-2-基)-5-(4-磺基苯基)-2H-四唑,内部盐)(MTS)测定。本研究结果表明UMR-106细胞在多孔PHBV基质上更加激增,多孔PHBV膜是骨组织工程应用的有希望的材料。

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