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

被引:58
作者
Behnam, Behzad [1 ]
Shier, Wayne T. [2 ]
Nia, Azadeh Hashem [1 ,3 ]
Abnous, Khalil [1 ]
Ramezani, Mohammad [4 ]
机构
[1] Mashhad Univ Med Sci, Sch Pharm, Pharmaceut Reseach Ctr, Mashhad, Iran
[2] Univ Minnesota Twin Cities, Dept Med Chem, Minneapolis, MN 55455 USA
[3] Ferdowsi Univ Mashhad, Fac Sci, Dept Chem, Mashhad, Iran
[4] Mashhad Univ Med Sci, Sch Pharm, Nanotechnol Res Ctr, Mashhad, Iran
关键词
Single-walled carbon nanotubes; Polyethyleneimine; Gene delivery; Non-viral vector; In vivo; IN-VITRO; DRUG-DELIVERY; TRANSFECTION EFFICIENCY; POLY(ETHYLENE GLYCOL); SIRNA DELIVERY; POLYETHYLENIMINE; DNA; VIVO; VECTOR; CELLS;
D O I
10.1016/j.ijpharm.2013.06.057
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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). PEls 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 NIP 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. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:204 / 215
页数:12
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