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In vitro evaluation of biomimetic chitosan-calcium phosphate scaffolds with potential application in bone tissue engineering

机译:仿生壳聚糖磷酸钙支架的体外评价及其在骨组织工程中的潜在应用

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This work reports on the physicochemical properties and in vitro cytotoxicity assessment of chitosan-calcium phosphate (Cs-CP) scaffolds for bone tissue engineering, which were synthesized by a novel biomimetic co-precipitation method. X-ray diffraction (XRD) along with scanning electron microscopy (SEM) analysis confirmed the porous morphology of the scaffolds and the amorphous nature of the inorganic phase with different crystallite sizes and the formation of various forms of calcium phosphate. Compressive mechanical testing revealed that the Young's modulus of the biomaterials is in the range of human trabecular bone. In vitro tests were performed on the biomaterials for up to 14 days to study the behavior of the osteoblast-like human cell line (MG63), primary human osteoblasts (HOS) and human dermal microvascular endothelial cells (HDMEC). The cytotoxicity was evaluated by the MTS assay for cell metabolism and the detection of membrane integrity (lactate dehydrogenase-LDH release). An expression of the vascular endothelial growth factor (VEGF) in the cell supernatants was quantified by ELISA. Cell viability gave values close to untreated controls for MG63 and HOS, while in the case of HDMEC the viability after 2 weeks in the cell culture was between 80-90%. The cytotoxicity induced by the Cs-CP scaffolds on MG63, HOS and HDMEC in vitro was evaluated by the amount of LDH released, which is a sensitive and accurate marker for cellular toxicity. The increased levels of VEGF obtained in the osteoblast culture highlights its important role in the regulation of vascularization and bone remodeling. The biological responses of the Cs-CP scaffolds demonstrate a similar proliferation and differentiation characteristics of the cells comparable to the controls. These results reveal that biomimetic Cs-CP composite scaffolds are promising biomaterials for bone tissue engineering; their in vivo response remains to be tested.
机译:这项工作报告了用于骨组织工程的壳聚糖磷酸钙(Cs-CP)支架的理化性质和体外细胞毒性评估,这些支架是通过新型仿生共沉淀方法合成的。 X射线衍射(XRD)以及扫描电子显微镜(SEM)分析证实了支架的多孔形态以及具有不同微晶尺寸的无机相的非晶态性质以及各种形式的磷酸钙的形成。压缩机械测试表明,该生物材料的杨氏模量在人类小梁骨的范围内。在生物材料上进行了长达14天的体外测试,以研究成骨细胞样人细胞系(MG63),原代人成骨细胞(HOS)和人皮肤微血管内皮细胞(HDMEC)的行为。通过用于细胞代谢的MTS分析和膜完整性(乳酸脱氢酶-LDH释放)的检测来评估细胞毒性。通过ELISA定量细胞上清液中的血管内皮生长因子(VEGF)的表达。细胞活力的值接近未处理的MG63和HOS对照,而在HDMEC情况下,细胞培养2周后的活力在80-90%之间。通过释放的LDH量评估Cs-CP支架在体外对MG63,HOS和HDMEC诱导的细胞毒性,LDH是细胞毒性的敏感而准确的标志物。在成骨细胞培养物中获得的VEGF水平升高,突显了其在调节血管形成和骨骼重塑中的重要作用。 Cs-CP支架的生物学反应表明,与对照组相比,细胞具有相似的增殖和分化特性。这些结果表明仿生的Cs-CP复合支架是用于骨组织工程的有前途的生物材料。它们的体内反应仍有待测试。

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