Folic-Acid-Targeted Self-Assembling Supramolecular Carrier for Gene Delivery

被引:23
|
作者
Liao, Rongqiang [1 ]
Yi, Shouhui [2 ]
Liu, Manshuo [1 ]
Jin, Wenling [1 ]
Yang, Bo [1 ]
机构
[1] Kunming Univ Sci & Technol, Fac Life Sci & Technol, Kunming 650500, Peoples R China
[2] Chongqing Canc Hosp, Dept Oncol, Chongqing 400011, Peoples R China
基金
中国国家自然科学基金;
关键词
cyclodextrins; drug delivery; gene carriers; polyethylenimine; self-assembly; NANOPARTICLES; PARTICLES; VECTOR; PEGYLATION; COMPLEXES; DESIGN; CELLS; PEI;
D O I
10.1002/cbic.201500208
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A targeting gene carrier for cancer-specific delivery was successfully developed through a multilayer bricks-mortar strategy. The gene carrier was composed of adamantane-functionalized folic acid (FA-AD), an adamantane-functionalized poly(ethylene glycol) derivative (PEG-AD), and -cyclodextrin-grafted low-molecular-weight branched polyethylenimine (PEI-CD). Carriers produced by two different self-assembly schemes, involving either precomplexation of the PEI-CD with the FA-AD and PEG-AD before pDNA condensation (Method A) or pDNA condensation with the PEI-CD prior to addition of the FA-AD and PEG-AD to engage host-guest complexation (Method B) were investigated for their ability to compact pDNA into nanoparticles. Cell viability studies show that the material produced by the Method A assembly scheme has lower cytotoxicity than branched PEI 25 kDa (PEI-25KD) and that the transfection efficiency is maintained. These findings suggest that the gene carrier, based on multivalent host-guest interactions, could be an effective, targeted, and low-toxicity carrier for delivering nucleic acid to target cells.
引用
收藏
页码:1622 / 1628
页数:7
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