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Glycosaminoglycan-functionalized gold nanorods: interactions with cardiac cells and type I collagen

机译:糖胺聚糖功能化的金纳米棒:与心肌细胞和I型胶原蛋白的相互作用。

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摘要

The sulfated glycosaminoglycans (sGAG) heparin and chondroitin sulfate (CS) were immobilized on the surfaces of gold nanorods as part of a polyelectrolyte multilayer. The effects of these nanomaterials on the self-assembly of type I collagen were examined by turbidity assays and microscopy, and desorption of sGAG from nanomaterial-collagen composites was quantified biochemically. The interactions of sGAG-coated nanorods with cardiac cells were also explored through a collagen gel contraction assay and confocal microscopy. In contrast to soluble forms of sGAG, sGAG-coated nanorods consistently accelerated collagen fibrillogenesis. Soluble heparin, and heparin- and CS-coated nanorods inhibited cell-mediated contraction of collagen gels, whereas soluble CS did not. Both heparin and CS-coated nanorods were detected in the peri- and/or intra-cellular compartments of the cells, but there was no evidence of cytotoxicity over 72 h of culture. These results indicate that biological polyanions, such as sGAG, may be useful in the modification of nanoparticle surface chemistry for biological and/or therapeutic applications.
机译:硫酸化的糖胺聚糖(sGAG)肝素和硫酸软骨素(CS)被固定在金纳米棒的表面上,作为聚电解质多层膜的一部分。通过浊度分析和显微镜检查,检查了这些纳米材料对I型胶原自组装的影响,并通过生化定量了sGAG从纳米材料-胶原蛋白复合物中的解吸。 sGAG涂层的纳米棒与心肌细胞的相互作用也通过胶原蛋白凝胶收缩测定和共聚焦显微镜进行了探讨。与可溶性形式的sGAG相比,sGAG包被的纳米棒持续促进胶原原纤维形成。可溶性肝素,肝素和CS包覆的纳米棒抑制细胞介导的胶原蛋白凝胶收缩,而可溶性CS则不然。肝素和CS包被的纳米棒均在细胞的周和/或细胞内区室中被检测到,但是在培养72小时后没有细胞毒性的证据。这些结果表明,诸如sGAG的生物聚阴离子可用于修饰纳米颗粒表面化学以用于生物学和/或治疗应用。

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