Bioreducible Guanidinylated Polyethylenimine for Efficient Gene Delivery

被引:14
作者
Lee, Duhwan [1 ,2 ]
Lee, Yeong Mi [1 ,2 ]
Jeong, Cherlhyun [3 ]
Lee, Jun [4 ]
Kim, Won Jong [1 ,2 ]
机构
[1] Pohang Univ Sci & Technol POSTECH, Inst Basic Sci, Ctr Self Assembly & Complex, Pohang 790784, South Korea
[2] Pohang Univ Sci & Technol POSTECH, Dept Chem, Pohang 790784, South Korea
[3] Korea Inst Sci & Technol KIST, Biomed Res Inst, Ctr Theragnosis, Seoul 136791, South Korea
[4] Wonkwang Univ, Wonkwang Bone Regenerat Res Inst, Sch Dent, Dept Oral & Maxillofacial Surg, Iksan 570749, South Korea
关键词
cell-penetrating peptides; gene delivery; gene expression; guanidine; polycations; redox chemistry; CELL-PENETRATING PEPTIDES; LOW-MOLECULAR-WEIGHT; TRANSFECTION EFFICIENCY; CATIONIC POLYMER; VECTORS; SYSTEMS; NANOCONSTRUCT; TRANSPORTERS; DESIGN; SIZE;
D O I
10.1002/cmdc.201402293
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Cationic polymers are known to afford efficient gene transfection. However, cytotoxicity remains a problem at the molecular weight for optimal DNA delivery. As such, optimized polymeric gene delivery systems are still a sought-after research goal. A guanidinylated bioreducible branched polyethylenimine (GBPEI-SS) was synthesized by using a disulfide bond to crosslink the guanidinylated BPEI (GBPEI). GBPEI-SS showed sufficient plasmid DNA (pDNA) condensation ability. The physicochemical properties of GBPEI-SS demonstrate that it has the appropriate size (approximate to 200nm) and surface potential (approximate to 30mV) at a nitrogen-to-phosphorus ratio of 10. No significant toxicity was observed, possibly due to bioreducibility and to the guanidine group delocalizing the positive charge of the primary amine in BPEI. Compared with the nonguanidinylated analogue, BPEI-SS, GBPEI-SS showed enhanced transfection efficiency owing to increased cellular uptake and efficient pDNA release by cleavage of disulfide bonds. This system is very efficient for delivering pDNA into cells, thereby achieving high transfection efficiency and low cytotoxicity.
引用
收藏
页码:2718 / 2724
页数:7
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