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首页> 外文期刊>Journal of Materials Chemistry, B. materials for biology and medicine >RGDS covalently surfaced nanodiamond as a tumor targeting carrier of VEGF-siRNA: synthesis, characterization and bioassay
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RGDS covalently surfaced nanodiamond as a tumor targeting carrier of VEGF-siRNA: synthesis, characterization and bioassay

机译:RGDS共价表面沉积的纳米金刚石作为VEGF-siRNA的肿瘤靶向载体:合成,表征和生物测定

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摘要

A nonviral tumor targeting vector for siRNA transfer is of importance. Here, a novel delivery system consisting of a covalent conjugate of NDCO-RGDS and VEGF-siRNA, NDCO-RGDS/VEGF-siRNA, was presented. In vitro, NDCO-RGDS/VEGF-siRNA released and transferred VEGF-siRNA in a long-acting manner. Compared to the control, NDCO-RGDS/VEGF-siRNA decreased the expression of VEGF mRNA and protein in HeLa cells by 88.41 +/- 3.49% and 83.94 +/- 2.00%, respectively. In vivo, NDCO-RGDS/VEGF-siRNA exhibited gene silencing and slowed tumor growth. FT-MS spectrum analysis revealed that NDCO-RGDS/VEGF-siRNA mainly distributed in tumor tissue of the treated S180 mice. Therefore NDCO-RGDS could be considered a promising nonviral tumor-targeting vector for siRNA transfer in tumor therapy.
机译:用于siRNA转移的非病毒肿瘤靶向载体非常重要。在这里,提出了由NDCO-RGDS和VEGF-siRNA的共价结合物NDCO-RGDS / VEGF-siRNA组成的新型递送系统。在体外,NDCO-RGDS / VEGF-siRNA以长效方式释放并转移了VEGF-siRNA。与对照组相比,NDCO-RGDS / VEGF-siRNA使HeLa细胞中VEGF mRNA和蛋白的表达分别降低了88.41 +/- 3.49%和83.94 +/- 2.00%。在体内,NDCO-RGDS / VEGF-siRNA表现出基因沉默并减慢了肿瘤的生长。 FT-MS光谱分析表明,NDCO-RGDS / VEGF-siRNA主要分布在治疗的S180小鼠的肿瘤组织中。因此,NDCO-RGDS可以被认为是在肿瘤治疗中用于siRNA转移的有希望的非病毒靶向肿瘤载体。

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