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Magnetic Mechanotransduction of Mesenchymal Stem Cells via a Highly Fluorescent Magnetic Micro Patterned Anti-Microbial Composite Scaffold

机译:间充质干细胞磁力机械调节通过高荧光磁性微观图案抗微生物复合支架支架

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Mesenchymal stem cells differentiates into different phenotype in the process of development or repair different organs in presence of various signals including physical stimulus. Osteogenesis is a complex process which involves not only growth factors like BMP-2 and RunX-2 but also requires physical stimuli like mechanical stretch. However, it is difficult for a tissue engineering scaffold to be mechanically stimulated especially in an in vivo system. In this context a micropattemed nanocomposite scaffold is fabricated which incorporated highly luminescent magnetic iron oxide nanoparticles and nanosilver doped hydroxyapatite nanoparticles. The nanoparticles were synthesized in hydrothermal route and characterized via TEM, SEM, EDX, FTIR, Raman, XPS, UV Vis spectroscopy, fluorescence spectroscopy and SQUID. The scaffold preparation was characterized via SEM, rheology, AFM and mechanical testing measurement. The final fabrication was a 3d printed lattice structured scaffold. The cell culture evaluation was performed in vitro via rat bone marrow derived stem cells using MTT assay, fluorescence microscopy, SEM, ALP assay, DNA quantification assay, o-cresolphthalein Ca deposition assay and PCR based gene expression study. The antimicrobial activity study was conducted against S aureus and E Coli. Cell cultured scaffolds were implanted subcutaneously on albino rats on different time intervals. Post sacrifice the sections were evaluated for bone growth via histology and immuno histochemistry study. In all the biological study 1 mT rare earth magnets were used to provide static magnetic field.
机译:间充质干细胞在发生包括物理刺激的各种信号的情况下在发育过程中分化为不同的器官的不同表型。成骨是一种复杂的过程,不仅涉及BMP-2和Runx-2等生长因子,而且还需要像机械拉伸等物理刺激。然而,难以将组织工程支架尤其在体内系统中机械刺激。在本文中,制造了一种微渗透型纳米复合材料支架,其掺入高发光磁性氧化铁纳米颗粒和纳米单体掺杂羟基磷灰石纳米颗粒。在水热途径中合成纳米颗粒,并通过TEM,SEM,EDX,FTIR,拉曼,XPS,UV Vis光谱,荧光光谱和鱿鱼。通过SEM,流变学,AFM和机械测试测量表征支架制剂。最终的制造是3D印刷晶格结构脚手架。通过使用MTT测定,荧光显微镜,SEM,ALP测定,DNA定量测定,O-Crsolphthalein Ca沉积测定和PCR基基因表达研究,通过大鼠骨髓衍生的干细胞体外进行细胞培养评估。对抗AUREUS和E COLI进行抗菌活性研究。细胞培养的支架在不同的时间间隔上皮下植入白化大鼠。牺牲后术后通过组织学和免疫组织化学研究评估骨骼生长的部分。在所有生物学研究中,1 MT稀土磁铁用于提供静磁场。

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