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Effect of testosterone incorporation on cell proliferation and differentiation for polymer-bioceramic composites

机译:睾酮掺入对聚合物-生物陶瓷复合材料细胞增殖和分化的影响

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摘要

In the current study, we characterized the polycaprolactone (PCL), poly(lactic acid-co-glycolic acid) (PLGA), and biphasic calcium phosphate (BCP) composites coated with testosterone propionate (T) using Fourier transform infrared spectroscopy (FTIR) and powder X-ray diffraction (XRD). Osteoblastic cells were seeded with PCL/BCP, PCL/BCP/T, PLGA/PCL/BCP and PLGA/PCL/ BCP/T scaffolds, and cell viability, proliferation, differentiation and adhesion were analyzed. The results of physic-chemical experiments showed no displacements or suppression of bands in the FTIR spectra of scaffolds. The XRD patterns of the scaffolds showed an amorphous profile. The osteoblastic cells viability and proliferation increased in the presence of composites with testosterone over 72 h, and were significantly greater when PLGA/PCL/ BCP/T scaffold was tested against PCL/BCP/T. Furthermore alkaline phosphatase production was significantly greater in the same group. In conclusion, the PLGA/PCL/ BCP scaffold with testosterone could be a promising option for bone tissue applications due to its biocompatibility and its stimulatory effect on cell proliferation.
机译:在当前的研究中,我们使用傅立叶变换红外光谱(FTIR)对涂有丙酸睾丸酮(T)的聚己内酯(PCL),聚乳酸-乙醇酸(PLGA)和双相磷酸钙(BCP)复合材料进行了表征和粉末X射线衍射(XRD)。将成骨细胞植入PCL / BCP,PCL / BCP / T,PLGA / PCL / BCP和PLGA / PCL / BCP / T支架,并分析细胞活力,增殖,分化和粘附。物理化学实验的结果表明,在支架的FTIR光谱中没有位移或谱带的抑制。支架的XRD图谱显示无定形轮廓。在含有睾丸酮的复合物存在下,成骨细胞的生存能力和增殖在72小时内增加,并且当针对PCL / BCP / T测试PLGA / PCL / BCP / T支架时,成骨细胞的生存能力和增殖显着增加。此外,在同一组中碱性磷酸酶的产量明显更高。总之,具有睾丸激素的PLGA / PCL / BCP支架由于其生物相容性及其对细胞增殖的刺激作用,可能成为骨组织应用的有前途的选择。

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  • 来源
    《Journal of materials science》 |2012年第11期|2751-2759|共9页
  • 作者单位

    Departamento de Odontologia Restauradora, Faculdade de Odontologia, Universidade Federal de Minas Gerais, Av. Antonio Carlos, 6627, Belo Horizonte, MG 31270901, Brazil;

    Departamento de Qufmica, Instituto de Ciencias Exatas, Universidade Federal de Minas Gerais, Belo Horizonte. MG, Brazil;

    Departamento de Qufmica, Instituto de Ciencias Exatas, Universidade Federal de Minas Gerais, Belo Horizonte. MG, Brazil;

    Departamento de Qufmica, Instituto de Ciencias Exatas, Universidade Federal de Minas Gerais, Belo Horizonte. MG, Brazil;

    Departamento de Clinica Odontologica, Cirurgia e Patologia, Faculdade de Odontologia, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil;

    Departamento de Odontologia Restauradora, Faculdade de Odontologia, Universidade Federal de Minas Gerais, Av. Antonio Carlos, 6627, Belo Horizonte, MG 31270901, Brazil,Department of Restorative Dentistry, Universidade Federal de Minas Gerais, Av. Antonio Carlos, 6627, Belo Horizonte, MG 31270901, Brazil;

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