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The design and features of apatite-coated chitosan microspheres as injectable scaffold for bone tissue engineering

机译:磷灰石包覆的壳聚糖微球作为骨组织工程注射支架的设计和特点

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In this paper we developed two types of chitosan-based microspheres with and without biomimetic apatite coatings and compared their potential as injectable scaffolds for bone regeneration. The microspheres were obtained by emulsion cross-linking (E0) and coacervate precipitation (C0), respectively. They were then biomimetically coated with apatite to become E1 and C1 microspheres. The physicochemical properties and biocompatibility of the microspheres were characterized. Both E0 and C0 microspheres presented favorable ranges of diameter, density and Rockwell hardness. However, there were differences in the degree of cross-linking, shape, morphology, degradation rate, swelling rate, pH value after PBS immersion and the biocompatibility between E0 and C0. The apatite coating was successfully prepared for both C0 and E0, which enhanced the attachment, proliferation and differentiation of MC3T3-E1 cells. In conclusion, our results suggest the feasibility of using chitosan microspheres as a potential injectable scaffold. Both the preparation method and the biomimetic apatite coating contribute to their biological properties.
机译:在本文中,我们开发了两种类型的带有和不带有仿生磷灰石涂层的壳聚糖基微球,并比较了它们作为可注射支架用于骨再生的潜力。分别通过乳液交联(E0)和凝聚层沉淀(C0)获得微球。然后用磷灰石仿生地涂覆它们,成为E1和C1微球。表征了微球的理化性质和生物相容性。 E0和C0微球均具有良好的直径,密度和洛氏硬度范围。但是,PBS浸泡后的交联度,形状,形态,降解率,溶胀率,pH值以及E0和C0之间的生物相容性存在差异。成功为C0和E0制备了磷灰石涂层,从而增强了MC3T3-E1细胞的附着,增殖和分化。总之,我们的结果表明使用壳聚糖微球作为潜在的可注射支架的可行性。制备方法和仿生磷灰石涂层均有助于它们的生物学性质。

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