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Novel conductive polypyrrole/silk fibroin scaffold for neural tissue repair

机译:用于神经组织修复的新型导电聚吡咯/丝素蛋白支架

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摘要

Three dimensional (3D) bioprinting,which involves depositing bioinks (mixed biomaterials) layer by layer to form computer-aided designs,is an ideal method for fabricating complex 3D biological structures.However,it remains challenging to prepare biomaterials with micro-nanostructures that accurately mimic the nanostructural features of natural tissues.A novel nanotechnological tool,electrospinning,permits the processing and modification of proper nanoscale biomaterials to enhance neural cell adhesion,migration,proliferation,differentiation,and subsequent nerve regeneration.The composite scaffold was prepared by combining 3D bioprinting with subsequent electrochemical deposition of polypyrrole and electrospinning of silk fibroin to form a composite polypyrrole/silk fibroin scaffold.Fourier transform infrared spectroscopy was used to analyze scaffold composition.The surface morphology of the scaffold was observed by light microscopy and scanning electron microscopy.A digital multimeter was used to measure the resistivity of prepared scaffolds.Light microscopy was applied to observe the surface morphology of scaffolds immersed in water or Dulbecco's Modified Eagle's Medium at 37℃ for 30 days to assess stability.Results showed characteristic peaks of polypyrrole and silk fibroin in the synthesized conductive polypyr-srole/silk fibroin scaffold,as well as the structure of the electrospun nanofiber layer on the surface.The electrical conductivity was 1 × 10-5-1 × 10-3 S/cm,while stability was 66.67%.A 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide assay was employed to measure scaffold cytotoxicity in vitro.Fluorescence microscopy was used to observe EdU-labeled Schwann cells to quantify cell proliferation.Immunohistochemistry was utilized to detect S100β immunoreactivity,while scanning electron microscopy was applied to observe the morphology of adherent Schwann cells.Results demonstrated that the polypyrrole/silk fibroin scaffold was not cytotoxic and did not affect Schwann cell proliferation.Moreover,filopodia formed on the scaffold and Schwann cells were regularly arranged.Our findings verified that the composite polypyrrole/silk fibroin scaffold has good biocompatibility and may be a suitable material for neural tissue engineering.
机译:三维(3D)生物打印涉及一层一层地沉积生物墨水(混合生物材料)以形成计算机辅助设计,是制造复杂3D生物结构的理想方法。然而,制备具有微纳米结构的生物材料仍然具有挑战性模拟自然组织的纳米结构特征。一种新型的纳米技术工具,静电纺丝,允许对适当的纳米级生物材料进行加工和修饰,以增强神经细胞的粘附,迁移,增殖,分化和随后的神经再生。结合3D生物打印制备复合支架聚吡咯的电化学沉积和丝素蛋白的静电纺丝形成聚吡咯/丝素蛋白复合支架。傅里叶变换红外光谱分析支架的组成,通过光学显微镜和扫描电子显微镜观察支架的表面形态。万用表w用光学显微镜观察37℃下浸入水或Dulbecco's改良Eagle's培养基中30天的支架表面形态,以评估其稳定性。结果显示,支架中的聚吡咯和丝素蛋白具有特征峰。合成的导电聚吡咯/丝素蛋白支架,以及表面电纺纳米纤维层的结构。电导率为1×10-5-1×10-3 S / cm,稳定性为66.67%.A采用3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2-H-四唑溴化物测定体外支架的细胞毒性,荧光显微镜观察EdU标记的施万细胞对细胞的定量免疫组织化学法检测S100β的免疫反应性,扫描电镜观察粘附的雪旺细胞的形态,结果表明聚吡咯/丝素蛋白支架无细胞毒作用。不影响雪旺氏细胞的增殖。此外,有规律地排列在支架上的丝状伪足和雪旺氏细胞。我们的发现证实,聚吡咯/丝素蛋白复合物支架具有良好的生物相容性,可能是神经组织工程的合适材料。

著录项

  • 来源
    《中国神经再生研究(英文版)》 |2018年第8期|1455-1464|共10页
  • 作者单位

    Key Laboratory of Science and Technology of Eco-textiles, Ministry of Education, Jiangnan University, Wuxi, Jiangsu Province, China;

    Key Laboratory of Neuroregeneration, Co-innovation Center of Neuroregeneration, Nantong University, Nantong, Jiangsu Province, China;

    Medical School, Nantong University, Nantong, Jiangsu Province, China;

    Medical School, Nantong University, Nantong, Jiangsu Province, China;

    Wen Zheng College, Soochow University, Suzhou, Jiangsu Province, China;

    Key Laboratory of Science and Technology of Eco-textiles, Ministry of Education, Jiangnan University, Wuxi, Jiangsu Province, China;

    Key Laboratory of Neuroregeneration, Co-innovation Center of Neuroregeneration, Nantong University, Nantong, Jiangsu Province, China;

    Key Laboratory of Science and Technology of Eco-textiles, Ministry of Education, Jiangnan University, Wuxi, Jiangsu Province, China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-19 04:25:49
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