PAMAM conjugated chitosan through naphthalimide moiety for enhanced gene transfection efficiency

被引:26
作者
Sarkar, Kishor [1 ]
Kundu, P. P. [1 ]
机构
[1] Univ Calcutta, Dept Polymer Sci & Technol, Kolkata 700009, W Bengal, India
关键词
Chitosan; PAMAM dendrimer; Cytotoxicity; In vitro; Transfection; N-MALEATED CHITOSAN; VIRAL VECTORS; CATIONIC POLYMERS; MOLECULAR-WEIGHT; DELIVERY VECTORS; THERAPY PROGRESS; IN-VITRO; POLYETHYLENIMINE; DENDRIMERS; PROSPECTS;
D O I
10.1016/j.carbpol.2013.06.006
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Development of efficient and safe gene carrier is the main hurdle for successful gene therapy till date. Poor water solubility and low transfection efficiency of chitosan are the main drawbacks to be efficient gene carrier for successful gene therapy. In this work, PAMAM conjugated chitosan was prepared through naphthalimide moiety by simple substitution reaction. The synthesis of the chitosan conjugates was confirmed by FTIR, H-1 NMR and XRD analyses. The conjugates showed enhanced DNA binding capability compared to that of unmodified chitosan. Moreover, the conjugates showed minimal cytotoxicity compared to that of polyethyleneimine (PEI, 25 kDa) and also showed good blood compatibility with negligible haemolysis. The transfection efficiency of the conjugate was significantly increased compared to that of unmodified chitosan and it also surpassed the transfection efficiency by PEI. Therefore, PAMAM conjugated chitosan can be used safely as alternate efficient gene delivery vector in gene therapy. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:495 / 504
页数:10
相关论文
共 50 条
  • [1] The Possible "Proton Sponge" Effect of Polyethylenimine (PEI) Does Not Include Change in Lysosomal pH
    Benjaminsen, Rikke V.
    Mattebjerg, Maria A.
    Henriksen, Jonas R.
    Moghimi, S. Moein
    Andresen, Thomas L.
    [J]. MOLECULAR THERAPY, 2013, 21 (01) : 149 - 157
  • [2] Gene Therapy for Cancer Treatment: Past, Present and Future
    Cross, Deanna
    Burmester, James K.
    [J]. CLINICAL MEDICINE & RESEARCH, 2006, 4 (03) : 218 - 227
  • [3] Gene Therapy Using Adeno-Associated Virus Vectors
    Daya, Shyam
    Berns, Kenneth I.
    [J]. CLINICAL MICROBIOLOGY REVIEWS, 2008, 21 (04) : 583 - 593
  • [4] Cationic liposomes for gene delivery:: From biophysics to biological applications
    de Lima, MCP
    Neves, S
    Filipe, A
    Düzgünes, N
    Simoes, S
    [J]. CURRENT MEDICINAL CHEMISTRY, 2003, 10 (14) : 1221 - 1231
  • [5] Gene Therapy for Parkinson's Disease
    Denyer, Rachel
    Douglas, Michael R.
    [J]. PARKINSONS DISEASE, 2012, 2012
  • [6] Dishart KL, 2003, J BIOMED BIOTECHNOL, P138
  • [7] Dendrimers in gene delivery
    Dufès, C
    Uchegbu, IF
    Schätzlein, AG
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2005, 57 (15) : 2177 - 2202
  • [8] Non-viral gene delivery carrier and its three-dimensional transfection system
    He, Cai-Xia
    Tabata, Yasuhiko
    Gao, Jian-Qing
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2010, 386 (1-2) : 232 - 242
  • [9] Transfection efficiency of chitosan vectors: Effect of polymer molecular weight and degree of deacetylation
    Huang, M
    Fong, CW
    Khor, E
    Lim, LY
    [J]. JOURNAL OF CONTROLLED RELEASE, 2005, 106 (03) : 391 - 406
  • [10] Cationic carriers of genetic material and cell death: A mitochondrial tale
    Hunter, A. Christy
    Moghimi, S. Moein
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2010, 1797 (6-7): : 1203 - 1209