Effects of hydrophobic and hydrophilic modifications on gene delivery of amphiphilic chitosan based nanocarriers

被引:123
作者
Wang, Bingqing [1 ]
He, Chunbai [1 ]
Tang, Cui [1 ]
Yin, Chunhua [1 ]
机构
[1] Fudan Univ, State Key Lab Genet Engn, Dept Pharmaceut Sci, Sch Life Sci, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
Amphiphilic chitosan based nanocarriers; Hydrophobic modification; Hydrophilic modification; Self-assembled nanocomplexes; Gene delivery; Transfection; TRANSFECTION EFFICIENCY; IN-VITRO; INTRACELLULAR TRAFFICKING; POLY(BETA-MALIC ACID); TRIMETHYL CHITOSAN; LINOLEIC-ACID; NANOPARTICLES; DERIVATIVES; CARRIER; DNA;
D O I
10.1016/j.biomaterials.2011.03.003
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The structure activity relationships between hydrophobic and hydrophilic modification on chitosan and resultant physicochemical properties along with performances in dealing with critical gene delivery barriers were investigated through amphiphilic linoleic acid(LA) and poly (beta-malic acid) (PMLA) double grafted chitosan (LMC)/plasmid DNA (pDNA) nanocomplexes. LMC polymers with various LA and PMLA substitution degrees were synthesized and their hydrophilicity/hydrophobicity was characterized. Compared to chitosan, LMC nanoparticles retained the pDNA binding ability at pH 5.5 when they formed nanocomplexes with pDNA encoding enhanced green fluorescence protein (pEGFP) and the resultant complexes showed diameters below 300 nm. Hydrophobic LA and hydrophilic PMLA substitution contributed to suppressed non-specific adsorption, reduced interactions inside LMC/pDNA nanocomplexes, and enhanced pDNA dissociation. However, enzymatic degradation resistance, cell adsorption, and cellular uptake through clathrin-mediated pathway were promoted by hydrophobic LA grafting while being inhibited by hydrophilic PMLA substitution. In vitro transfection assay suggested the optimal LMC/pEGFP nanocomplexes mediated an 8.0-fold improved transfection compared to chitosan/pEGFP nanocomplexes. The 4.2-fold and 2.2-fold higher intramuscular gene expression in mice compared to chitosan/pEGFP and polyethyleneimine (PEI)/pEGFP nanocomplexes further demonstrated the superiority of LMC/pDNA nanocomplexes. Therefore, amphiphilic chitosan derivates with appropriate combination of hydrophobic and hydrophilic modification would be promising gene delivery nanocarriers. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4630 / 4638
页数:9
相关论文
共 32 条
  • [1] Poly(beta-malic acid): Obtaining high molecular weights by improvement of the synthesis route
    Cammas, S
    Renard, I
    Langlois, V
    Guerin, P
    [J]. POLYMER, 1996, 37 (18) : 4215 - 4220
  • [2] Deoxycholic acid-conjugated chitosan oligosaccharide nanoparticles for efficient gene carrier
    Chae, SY
    Son, S
    Lee, M
    Jang, MK
    Nah, JW
    [J]. JOURNAL OF CONTROLLED RELEASE, 2005, 109 (1-3) : 330 - 344
  • [3] Synthesis and characterization of chitosan-g-poly(ethylene glycol)-folate as a non-viral carrier for tumor-targeted gene delivery
    Chan, Peggy
    Kurisawa, Motoichi
    Chung, Joo Eun
    Yang, Yi-Yan
    [J]. BIOMATERIALS, 2007, 28 (03) : 540 - 549
  • [4] Quantitative comparison of intracellular unpacking kinetics of polyplexes by a model constructed from quantum Dot-FRET
    Chen, Hunter H.
    Ho, Yi-Ping
    Jiang, Xuan
    Mao, Hai-Quan
    Wang, Tza-Huei
    Leong, Kam W.
    [J]. MOLECULAR THERAPY, 2008, 16 (02) : 324 - 332
  • [5] From controlled ring-opening polymerization to biodegradable aliphatic polyester:: Especially poly(β-malic acid) derivatives
    Coulembier, Olivier
    Degee, Philippe
    Hedrick, James L.
    Dubois, Philippe
    [J]. PROGRESS IN POLYMER SCIENCE, 2006, 31 (08) : 723 - 747
  • [6] Cell line-dependent internalization pathways and intracellular trafficking determine transfection efficiency of nanoparticle vectors
    Douglas, Kimberly L.
    Piccirillo, Ciriaco A.
    Tabrizian, Maryam
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2008, 68 (03) : 676 - 687
  • [7] Factors influencing the transfection efficiency of ultra low molecular weight chitosan/hyaluronic acid nanoparticles
    Duceppe, Nicolas
    Tabrizian, Maryam
    [J]. BIOMATERIALS, 2009, 30 (13) : 2625 - 2631
  • [8] Chitosan-based vector/DNA complexes for gene delivery: Biophysical characteristics and transfection ability
    Erbacher, P
    Zou, SM
    Bettinger, T
    Steffan, AM
    Remy, JS
    [J]. PHARMACEUTICAL RESEARCH, 1998, 15 (09) : 1332 - 1339
  • [9] Engineered Nanoscaled Polyplex Gene Delivery Systems
    Fernandez, Christian A.
    Rice, Kevin G.
    [J]. MOLECULAR PHARMACEUTICS, 2009, 6 (05) : 1277 - 1289
  • [10] Chitosan N-betainates/DNA self-assembly nanoparticles for gene delivery: In vitro uptake and transfection efficiency
    Gao, Yu
    Zhang, Zhiwen
    Chen, Lingli
    Gu, Wangwen
    Li, Yaping
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2009, 371 (1-2) : 156 - 162