首页> 外文期刊>Chemical and Pharmaceutical Bulletin >Improvements in Transfection Efficiency with Chitosan Modified Poly( DL -lactide-co-glycolide) Nanospheres Prepared by the Emulsion Solvent Diffusion Method, for Gene Delivery
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Improvements in Transfection Efficiency with Chitosan Modified Poly( DL -lactide-co-glycolide) Nanospheres Prepared by the Emulsion Solvent Diffusion Method, for Gene Delivery

机译:乳胶扩散法制备的壳聚糖修饰聚DL-丙交酯-乙交酯乙交酯纳米球用于基因传递的转染效率的提高

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This study sought to evaluate the in vitro transfection efficiency of plasmid DNA (pDNA)-loaded chitosan-modified poly( DL -lactide- co -glycolide) nanospheres (CS-PLGA NS) in a gene-delivery system. Using the emulsion solvent diffusion (ESD) method, pDNA-loaded PLGA NS was prepared and the surface of the PLGA NS was modified by binding to CS. Gene transfection ability of CS-PLGA NS was examined in A549 cells. The luciferase gene was used as a reporter gene. The pattern of luciferase activity by pDNA-loaded CS-PLGA NS was initially weak, but gradually grew stronger before decreasing activity. These phenomena should be in accordance with the sustained-release profile of pDNA from PLGA NS in the cytosol and the pDNA protection against DNase. Positively charged CS-PLGA NS was found, by 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2 H -tetrazolium, inner salt (MTS) assay, not to exhibit cytotoxicity on A549 cells. These results suggest that CS-PLGA NS are potential contributors to efficient pDNA delivery due to their increased interactions with cells and lack of cytotoxic effects.
机译:这项研究试图评估在基因传递系统中负载质粒DNA(pDNA)的壳聚糖修饰的聚(DL-丙交酯-共-乙交酯)纳米球(CS-PLGA NS)的体外转染效率。使用乳液溶剂扩散(ESD)方法,制备了装载pDNA的PLGA NS,并通过与CS结合来修饰PLGA NS的表面。在A549细胞中检查了CS-PLGA NS的基因转染能力。荧光素酶基因用作报告基因。加载pDNA的CS-PLGA NS的萤光素酶活性模式最初很弱,但在活性降低之前逐渐增强。这些现象应与PLGA NS中pDNA在细胞质中的缓释曲线和pDNA对DNase的保护作用相一致。通过3-(4,5-二甲基噻唑-2-基)-5-(3-羧基甲氧基苯基)-2-(4-磺基苯基)-2 H-四唑,内盐(MTS)发现带正电荷的CS-PLGA NS不能对A549细胞表现出细胞毒性。这些结果表明,CS-PLGA NS由于其与细胞的相互作用增强和缺乏细胞毒性作用而成为有效pDNA传递的潜在贡献者。

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