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Non-covalent functionalization of single-walled carbon nanotubes with modified polyethyleneimines for efficient gene delivery

机译:单壁碳纳米管的非共价功能化与改性聚乙烯亚胺的有效基因传递

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Functionalized carbon nanotubes (CNTs) have been recently emerged as important class of vectors for delivery of DNA and other biomolecules into various cells. In this study, single-walled carbon nanotubes (SWNTs) were functionalized by non-covalent binding of hydrophobic moieties, which were covalently linked to polyethyleneimines (PEIs). PEIs of three molecular weights (25, 10 and 1.8 kDa) were used. CNTs were functionalized with the PEI series either through phospholipid moiety (via a polyethyleneglycol linker) or through directly-attached long (18 carbons) or intermediate (10 carbons) hydrophobic alkyl moieties. All PEI-functionalized CNTs exhibited good stability and dispersibility in biological media. Visualizing of functionalized CNTs and lack of aggregation were confirmed by atomic force microscopy. The PEI derivatives bound to CNTs retained the ability to fully condense plasmid DNA at low N/P ratios and substantial buffering capacity in the endosomal pH range. PEI-functionalized CNTs exhibited increased transfection efficiency compared to underivatized PEIs up to 19-fold increase being observed in the functionalized CNT with the smallest PEI tested, the smallest hydrophobic attachment moiety tested and no linker. Also PEI-functionalized CNTs were effective gene delivery vectors in vivo following tail vein injection in mice with the largest expression occurring with the vector PEI-functionalized through a polyethyleneglycol linker.
机译:最近,功能化碳纳米管(CNTs)成为重要的一类载体,用于将DNA和其他生物分子传递到各种细胞中。在这项研究中,单壁碳纳米管(SWNTs)通过疏水部分的非共价结合功能化,疏水部分与聚乙烯亚胺(PEIs)共价连接。使用了三种分子量(25、10和1.8 kDa)的PEI。碳纳米管通过磷脂部分(通过聚乙二醇接头)或通过直接连接的长(碳原子数为18)或中间(碳原子数为10)的疏水烷基部分以PEI系列功能化。所有PEI官能化的CNT在生物介质中均表现出良好的稳定性和分散性。通过原子力显微镜证实功能化的CNT的可视化和缺乏聚集。与CNT结合的PEI衍生物保留了在低N / P比率下充分浓缩质粒DNA的能力以及在内体pH范围内的显着缓冲能力。与未衍生的PEI相比,PEI官能化的CNT表现出更高的转染效率,其中在测试的最小的PEI,测试的最小的疏水连接部分和无接头的情况下,在官能化的CNT中观察到高达19倍的增长。在小鼠尾静脉注射后,PEI功能化的CNTs也是体内有效的基因传递载体,其中表达最大的是通过聚乙二醇接头功能化的PEI功能化的载体。

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