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Synthesis and Characterization of Dexamethasone-Conjugated Linear Polyethylenimine as a Gene Carrier

Authors
Kim, HyunjungBae, Yun MiKim, Hyun AhHyun, HyesunYu, Gwang SigChoi, Joon SigLee, Minhyung
Issue Date
Jun-2010
Publisher
WILEY
Keywords
BRANCHED POLYETHYLENIMINE (BPEI); DEXAMETHASONE; GENE DELIVERY; LINEAR POLYETHYLENIMINE (PEI); TRANSFECTION
Citation
JOURNAL OF CELLULAR BIOCHEMISTRY, v.110, no.3, pp.743 - 751
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF CELLULAR BIOCHEMISTRY
Volume
110
Number
3
Start Page
743
End Page
751
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/174879
DOI
10.1002/jcb.22587
ISSN
0730-2312
Abstract
Linear polyethylenimine (25 kDa, LPEI25k) has been shown to be an effective non-viral gene carrier with higher transfection and lower toxicity than branched polyethylenimine (BPEI) of comparable molecular weight. In this study, dexamethasone was conjugated to LPE125k to improve the efficiency of gene delivery. Dexamethasone is a synthetic glucocorticoid receptor ligand. Dexamethasone-conjugated LPEI25k (LPEI-Dexa) was evaluated as a gene carrier in various cells. Gel retardation assays showed that LPEI-Dexa completely retarded plasmid DNA (pDNA) at a 0.75:1 weight ratio (LPEI/pDNA). LPEI-Dexa had the highest transfection efficiency at a 2:1 weight ratio (LPEI-Dexa/DNA). At this ratio, the size of the LPEI-Dexa/pDNA complex was approximately 125 nm and the zeta potential was 35 mV. LPEI-Dexa had higher transfection efficiency than LPEI and Lipofectamine 2000. In addition, the cytotoxicity of LPEI-Dexa was much lower than that of BPEI (25 kDa, BPEI25k). In conclusion, LPEI-Dexa has a high transfection efficiency and low toxicity and can therefore be used for non-viral gene delivery.
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