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Synthesis and Evaluation of Novel Chitosan Derivatives for Gene Delivery 被引量:1

Synthesis and Evaluation of Novel Chitosan Derivatives for Gene Delivery
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摘要 A series of novel water soluble chitosan derivatives as gene vectors was synthesized. The delivery systems were tested for their ability to form complexes with plasmid DNA by utilizing agarose gel electrophoresis, particle size analysis, zeta potential measurement and scanning electron microscopy. Furthermore, cytotoxicity of chitosan derivatives and transfection efficiency of polyplexes were evaluated in vitro. The experimental results showed that the novel chitosan derivatives had lower cytotoxicity, good DNA condensation, and higher transfection efficiencies compared to chitosan in both 293T and HeLa cell lines. It was indicated that these chitosan derivatives were promising candidates for non-viral gene vectors. A series of novel water soluble chitosan derivatives as gene vectors was synthesized. The delivery systems were tested for their ability to form complexes with plasmid DNA by utilizing agarose gel electrophoresis, particle size analysis, zeta potential measurement and scanning electron microscopy. Furthermore, cytotoxicity of chitosan derivatives and transfection efficiency of polyplexes were evaluated in vitro. The experimental results showed that the novel chitosan derivatives had lower cytotoxicity, good DNA condensation, and higher transfection efficiencies compared to chitosan in both 293T and HeLa cell lines. It was indicated that these chitosan derivatives were promising candidates for non-viral gene vectors.
出处 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2015年第4期852-858,共7页 武汉理工大学学报(材料科学英文版)
基金 Funded by the National Natural Science Foundation of China(Nos.21204071,51273156) the Natural Science Foundation of Hubei Province(2014CFB833) the Innovation Research Fund of Wuhan university of Technology(20121049720006)
关键词 gene vector transfection efficiency CHITOSAN non-viral vector gene vector transfection efficiency chitosan non-viral vector
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  • 1Dorothee VL, Hasselmann S, Hasselmann K. Gene Therapy for HIV Infection: What does It Need to Make It Work? [J]. Journal of Gene Medicine, 2006, 8:658-667.
  • 2Wong LF, Goodhead L, Part C, et al. Lentivirus-mediated Gene Transfer to the Central Nervous System: Therapeutic and Research Applications[J]. Human Gene Therapy, 2006, 17:1-9.
  • 3Pawliuk R, Westerman KA, Fabry ME, et al. Correction of Sickle Cell Disease in Transgenic Mouse Models by Gene Therapy [J]. Science, 2001, 294:2 368-2 372.
  • 4Lehrman S. Virus Treatment Questioned after Gene Therapy Death [J]. Nature, 1999,401:517-518.
  • 5Li S, Huang L. Non-viral Gene Therapy: Promises and Chall- enges[J]. Gene Therapy, 2000, 7:31-34.
  • 6Luo K, Li CX, Wang G, et al. Peptide Dendrimers as Efficient and Biocompatible Gene Delivery Vectors: Synthesis and in Vitro Characterization[J]. Journal of controlled release, 2011, 155:77-87.
  • 7Merdan T, Kopecek J, Kissel T. Prospects for Cationic Poly- mers in Gene and Oligonucleotide Therapy Against Cancer [J], Advanced Drug Delivery Reviews, 2002, 54:715-758.
  • 8Pack DW, Hoffman AS, Pun S, et al. Design and Development of Polymers for Gene Delivery[J]. Nature Reviews Drug Discovery, 2005, 4:589-593.
  • 9He YY, Cheng G, Xie L, et al. Polyethyleneimine/DNA Polyplexes with Reduction-sensitive Hyaluronic Acid Derivatives Shielding for Targeted Gene Delivery [J]. Biomaterials, 2013, 34:1 235-1 245.
  • 10Hu Y, Xu BH, Ji QX, et al. A Mannosylated Cell-penetrating Peptide-grafl-polyethylenimine as a Gene Delivery Vector [J]. Biomaterials, 2014, 35(13): 4 236-4 246.

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