...
首页> 外文期刊>MedChemComm >Evaluation of chemical modification effects on DNA plasmid transfection efficiency of singlewalled carbon nanotube-succinate- polyethylenimine conjugates as non-viral gene carriers
【24h】

Evaluation of chemical modification effects on DNA plasmid transfection efficiency of singlewalled carbon nanotube-succinate- polyethylenimine conjugates as non-viral gene carriers

机译:单壁碳纳米管 - 琥珀酸酯 - 聚乙烯亚胺缀合物作为非病毒基因载体的化学修饰对化学改性效应的评价

获取原文
获取原文并翻译 | 示例
           

摘要

Polyethylenimine (PEI) is a widely used non-viral vector for DNA delivery. One major obstacle of higher molecular weight PEIs is the increased cytotoxicity despite the improved transfection efficiency and numerous chemical modifications that have been reported to overcome this problem. Carbon nanotubes (CNT) are carbon nanomaterials capable of penetrating into cell membranes with no cytotoxic effects. Covalent and noncovalent functionalization methods have been used to improve their solubility in aqueous media. The idea of conjugating PEIs and CNT through different chemical bonds and linkers seems promising as it may result in highly effective carriers due to combination of the transfection ability of PEI with cell internalization of CNT. In this study, six different water-soluble PEI conjugates of single-walled carbon nanotubes (SWNTs) were prepared by grafting PEI with one of three molecular weights (1.8, 10 and 25 kDa) through succinate as a linker which refers to "an organic moiety through which a SWNT is conjugated to PEI." The succinate linker was introduced to the surface of SWNTs through two different chemical strategies: a) ester and b) acyl linkages. The resulting SWNT-PEI vectors were characterized by IR spectroscopy, thermogravimetric analysis (TGA) and SEM imaging. All synthesized carriers were evaluated and compared for their cytotoxicity and transfection efficiency in murine neuroblastoma cells as polyplexes with plasmid DNA for luciferase and green fluorescent protein (GFP). The most efficient carriers were prepared by attaching PEI with the lowest molecular weight (1.8 kDa) through acyl linkage, which gave a transfection efficiency 190-fold greater than that of the corresponding free PEI. Transfection efficiency was the highest in polyplexes prepared with acyl-linked conjugates in all the plasmid/vector ratios studied.
机译:聚乙烯菊氨酸(PEI)是用于DNA递送的广泛使用的非病毒载体。尽管改善了转染效率和据报道的许多化学修饰来克服这一问题,但较高分子量PeI的一个主要障碍是增加的细胞毒性。碳纳米管(CNT)是能够穿透到没有细胞毒性作用的细胞膜中的碳纳米材料。共价和非共价官能化方法已被用于改善其在水性介质中的溶解度。通过不同的化学键和接头缀合PeI和CNT的想法似乎有望,因为它可能导致高效的载体由于PEI的转染能力与CNT细胞内化的组合。在这项研究中,通过用琥珀酸盐作为链接剂将PEI嫁接PEI,通过琥珀酸盐将PEI嫁接PEI,以“有机”,通过琥珀酸盐中的一种(1.8,10和25kDa)制备单壁碳纳米管(SWNT)的六种不同水溶性PEI缀合物。 SWNT与PEI缀合的部分。“通过两种不同的化学策略将琥珀酸酯连接物引入SWNT的表面:a)酯和b)酰基键。由此产生的SWNT-PEI载体的特征在于IR光谱,热重分析(TGA)和SEM成像。评估所有合成的载体,并将其与鼠神经母细胞瘤细胞的细胞毒性和转染效率进行比较,因为具有用于荧光素酶和绿色荧光蛋白(GFP)的质粒DNA的络合物。通过将PEI与酰基键连接的最低分子量(1.8kDa)附着,通过酰基键将PEI与酰基键合来制备最有效的载体。转染效率是用酰基连接的缀合物在研究的所有质粒/载体比例中制备的多单双中最高。

著录项

  • 来源
    《MedChemComm》 |2017年第2期|共12页
  • 作者单位

    Pharmaceutical Research Center School of Pharmacy Mashhad University of Medical Sciences Mashhad Iran;

    Pharmaceutics Research Center Institute of Neuropharmacology Kerman University of Medical Sciences Kerman Iran;

    Pharmaceutical Research Center School of Pharmacy Mashhad University of Medical Sciences Mashhad Iran;

    Nanobiotechnology Group Department of Life Science Engineering Faculty of New Sciences and Technologies University of Tehran Tehran Iran;

    Department of Chemistry Faculty of Sciences Ferdowsi University of Mashhad Mashhad Iran;

    Department of Medicinal Chemistry University of Minnesota-Twin Cities Minneapolis MN 55455 USA;

    Pharmaceutical Research Center School of Pharmacy Mashhad University of Medical Sciences Mashhad Iran;

    Pharmaceutical Research Center School of Pharmacy Mashhad University of Medical Sciences Mashhad Iran;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

    Evaluation; modification; gene carriers;

    机译:评估;修改;基因载体;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号