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Preparation and characterization of cationic PLGA-PEGLf/DOPE nanoparticles for HO-1 gene delivery
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  • 作者:Yuanjian Song (12) biosongyuanjian@126.com
    Zhimin Zong (1)
    Hongzhi Liu (2)
    Xiangru Wen (2)
    Dashi Qi (2)
    Yang Du (2)
    Fang Zhang (2)
    Xianyong Wei (1) wei_xianyong@163.com
  • 关键词:Key words PLGA nanoparticles – ; PEGylation – ; gene delivery – ; lactoferrin
  • 刊名:Journal of Wuhan University of Technology--Materials Science Edition
  • 出版年:2012
  • 出版时间:April 2012
  • 年:2012
  • 卷:27
  • 期:2
  • 页码:217-221
  • 全文大小:419.3 KB
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  • 作者单位:1. Key Laboratory of Coal Processing and Efficient Utilization (Ministry of Education), China University of Mining & Technology, Xuzhou, 221008 China2. Department of Neurobiology, Xuzhou Medical College, Xuzhou, 221002 China
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Materials Science
    Chinese Library of Science
  • 出版者:Wuhan University, co-published with Springer
  • ISSN:1993-0437
文摘
Cationic nanoparticles (NPs) for gene delivery were successfully prepared by assembling carboxylation poly(lactic-co-glycolic acid) (PLGA), polyethylene glycol (PEG), L-α-Phosphatidylethanolamine (DOPE) and octadecyl quaternized carboxymethyl chitosans (OQCMC). Lactoferrin (Lf) was selected as a targeting ligand conjugated to PLGA via bifunctional PEG, yielding PLGA-PEG-Lf/DOPE NPs to be used for gene vectors. Fourier transform infrared spectroscopy (FTIR), UV and nuclear magnetic resonance (NMR) spectroscopy were performed to evaluate the synthesis of the vectors. The characteristics of the vectors loaded heme oxygenase (HO-1) gene were evaluated by transmission electron microscope (TEM), particle size analyser and fluorescent microscopy. The experimental results showed that the obtained vectors were spherical in shape with average particle size of 142.2 nm and zeta potentials of +16.4 mV. The vectors could protect the loaded gene from the degradation by nuclease. For 293T cells, there is high transfection efficiency of the vectors similar to liposome-2000. It can be concluded that the established cationic PLGA-PEG-Lf/DOPE NPs have potential gene delivery ability for gene therapy.

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