Author/Authors :
Xu، نويسنده , , Zhigang and Wan، نويسنده , , Xiaoping and Zhang، نويسنده , , Wei and Wang، نويسنده , , Zheng and Peng، نويسنده , , Rong and Tao، نويسنده , , Feng and Cai، نويسنده , , Lin and Li، نويسنده , , Ying and Jiang، نويسنده , , Qing and Gao، نويسنده , , Rong، نويسنده ,
Abstract :
Methoxy poly(ethylene glycol)–polyethylenimine–chitosan (mPEG–PEI–CS) was synthesized via chitosan conjugated with polyethylenimine and methoxy poly(ethylene glycol). The intermediates and final copolymer were characterized and confirmed by 1H NMR and FT-IR spectra. mPEG–PEI–CS was water soluble and its intrinsic viscosity was 0.446 dL/g. The contents of mPEG and PEI conjugated in the copolymer were 51.3% (w/w) and 28.9% (w/w), and the degree of substitution of PEI by mPEG was 176%. Gel electrophoresis confirmed that DNA was retained completely by the copolymer nanoparticles. The average diameter and zeta potential of mPEG–PEI–CS/DNA were 155 nm and 17.5 mV. The transfection of human embryonic kidney 293 (HEK293) cells proved that mPEG–PEI–CS/VRfat-1 plasmid had little toxicity on the growth and gene expression of cells, and the ratio of ω-3/ω-6 fatty acids was obviously increased after 72 h transfection compared to CS/VRfat-1 (P < 0.05). These indicated that mPEG–PEI–CS was a promising effective gene delivery and package molecule.
Keywords :
Chitosan , Polyethylenimine , Methoxy poly(ethylene glycol) , Gene carrier , Synthesis