Issue 12, 2010

Galactosyl conjugated N-succinyl-chitosan-graft-polyethylenimine for targeting gene transfer

Abstract

Through incorporating lactobionic acid (LA) bearing a galactose group to N-succinyl-chitosan-graft-polyethylenimine (NSC-g-PEI), NSC-g-PEI-LA copolymers were synthesized as gene vectors with hepatocyte targeting properties. The molecular weight and composition of NSC-g-PEI-LA copolymers were characterized using gel permeation chromatography (GPC) and 1H nuclear magnetic resonance spectroscopy (1H NMR) respectively. Agarose gel electrophoresis assays showed good DNA binding ability of NSC-g-PEI-LA, and the particle size of the NSC-g-PEI-LA/DNA complexes were between 150 and 400 nm as determined by a Zeta sizer. The NSC-g-PEI-LA/DNA complexes observed by scanning electron microscopy (SEM) exhibited a compact and spherical morphology. The zeta potentials of these complexes were increased with the weight ratio of NSC-g-PEI-LA/DNA. NSC-g-PEI-LA has a lower cytotoxicity than PEI (25 kDa) and the toxicity decreased with increasing substitution of LA. The transfection efficiency of different complexes was evaluated by luciferase assay. Compared with PEI (25 kDa) and NSC-g-PEI/DNA, NSC-g-PEI-LA showed good transfection activity and cell specificity to HepG2 cells. The results suggested that NSC-g-PEI-LA has the potential to be used as a safe and effective targeting gene vector.

Graphical abstract: Galactosyl conjugated N-succinyl-chitosan-graft-polyethylenimine for targeting gene transfer

Article information

Article type
Paper
Submitted
11 Jul 2010
Accepted
17 Aug 2010
First published
18 Oct 2010

Mol. BioSyst., 2010,6, 2529-2538

Galactosyl conjugated N-succinyl-chitosan-graft-polyethylenimine for targeting gene transfer

B. Lu, D. Wu, H. Zheng, C. Quan, X. Zhang and R. Zhuo, Mol. BioSyst., 2010, 6, 2529 DOI: 10.1039/C0MB00096E

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