Gene transfection efficacies of novel cationic gemini lipids possessing aromatic backbone and oxyethylene spacers

被引:52
作者
Bajaj, Avinash [1 ]
Kondaiah, Paturu [2 ]
Bhattacharya, Santanu [1 ,3 ]
机构
[1] Indian Inst Sci, Dept Organ Chem, Bangalore 560012, Karnataka, India
[2] Indian Inst Sci, Dept Mol Reprod Dev & Genet, Bangalore 560012, Karnataka, India
[3] JNCASR, Chem Biol Unit, Bangalore 560064, Karnataka, India
关键词
D O I
10.1021/bm700930y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Six novel gemini cationic lipids based on aromatic backbone, bearing n-C14H29 or n-C16H33 hydrocarbon chains, differing in the length of oxyethylene type spacers -CH2-(CH2-O-CH2)(m)-CH2- between each ammonium headgroups have been synthesized, where m varies from 1 to 3. Each of these lipids formed stable suspensions in aqueous media. Cationic liposomes were prepared from each of these lipids individually and as mixtures of each cationic lipid and DOPE. These were used as nonviral gene delivery agents. Transfection studies showed that among lipids bearing n-C14H29 chains, the transfection efficacies decreased with the increase in the length of the spacer, whereas in case of lipids bearing n-C16H33 chains, the transfection efficacies increased with the increase in the length of the spacer. Lipid bearing n-CIA, hydrocarbon chains with a [-(CH2-CH2-O-CH2-CH2-O-CH2- CH2-O-CH2-CH2H spacer was found to be a potent gene transfer, agent and its transfection was highly serum compatible even in the presence of 50% serum conditions.
引用
收藏
页码:991 / 999
页数:9
相关论文
共 50 条
  • [41] Miller AD, 1998, ANGEW CHEM INT EDIT, V37, P1769
  • [43] Synthesis of novel dimeric cationic lipids based on an aromatic backbone between the hydrocarbon chains and headgroup
    Paul, Bishwajit
    Bajaj, Avinash
    Indi, S. S.
    Bhattacharya, Santanu
    [J]. TETRAHEDRON LETTERS, 2006, 47 (47) : 8401 - 8405
  • [44] Kanamycin A-derived cationic lipids as vectors for gene transfection
    Sainlos, M
    Hauchecorne, M
    Oudrhiri, N
    Zertal-Zidani, S
    Aissaoui, A
    Vigneron, JP
    Lehn, JM
    Lehn, P
    [J]. CHEMBIOCHEM, 2005, 6 (06) : 1023 - 1033
  • [45] Novel pyridinium surfactants for efficient, nontoxic in vitro gene delivery
    VanDerWoude, I
    Wagenaar, A
    Meekel, AAP
    TerBeest, MBA
    Ruiters, MHJ
    Engberts, JBFN
    Hoekstra, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (04) : 1160 - 1165
  • [46] Gene therapy - promises, problems and prospects
    Verma, IM
    Somia, N
    [J]. NATURE, 1997, 389 (6648) : 239 - 242
  • [47] Synergistic effect between components of mixtures of cationic amphipaths in transfection of primary endothelial cells
    Wang, Li
    MacDonald, Robert C.
    [J]. MOLECULAR PHARMACEUTICS, 2007, 4 (04) : 615 - 623
  • [48] Improved cell viability of linear polyethylenimine through γ-cyclodextrin inclusion for effective gene delivery
    Yamashita, A
    Choi, HS
    Ooya, T
    Yui, N
    Akita, H
    Kogure, K
    Harashima, H
    [J]. CHEMBIOCHEM, 2006, 7 (02) : 297 - 302
  • [49] INACTIVATION OF E2A IN RECOMBINANT ADENOVIRUSES IMPROVES THE PROSPECT FOR GENE-THERAPY IN CYSTIC-FIBROSIS
    YANG, YP
    NUNES, FA
    BERENCSI, K
    GONCZOL, E
    ENGELHARDT, JF
    WILSON, JM
    [J]. NATURE GENETICS, 1994, 7 (03) : 362 - 369
  • [50] CELLULAR-IMMUNITY TO VIRAL-ANTIGENS LIMITS E1-DELETED ADENOVIRUSES FOR GENE-THERAPY
    YANG, YP
    NUNES, FA
    BERENCSI, K
    FURTH, EE
    GONCZOL, E
    WILSON, JM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (10) : 4407 - 4411