Hyperbranched PEGmethacrylate linear pDMAEMA block copolymer as an efficient non-viral gene delivery vector

被引:28
|
作者
Mathew, Asha [1 ]
Cao, Hongliang [1 ]
Collin, Estelle [1 ]
Wang, Wenxin [1 ]
Pandit, Abhay [1 ]
机构
[1] Natl Univ Ireland, Network Excellence Funct Biomat, Galway, Ireland
关键词
2-(Dimethylamino) ethyl methacrylate; Deactivation enhanced atom transfer radical polymerisation; Gene therapy; THERAPY; SYSTEMS; DNA; MICELLES; CARRIER; NEED; PEG;
D O I
10.1016/j.ijpharm.2012.05.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A unique hyperbranched polymeric system with a linear poly-2-dimethylaminoethyl methacrylate (pDMAEMA) block and a hyperbranched polyethylene glycol methyl ether methacrylate (PEGMEMA) and ethylene dimethacrylate (EGDMA) block was designed and synthesized via deactivation enhanced atom transfer radical polymerisation (DE-ATRP) for efficient gene delivery. Using this unique structure, with a linear pDMAEMA block, which efficiently binds to plasmid DNA (pDNA) and hyperbranched polyethylene glycol (PEG) based block as a protective shell, we were able to maintain high transfection levels without sacrificing cellular viability even at high doses. The transfection capability and cytotoxicity of the polymers over a range of pDNA concentration were analysed and the results were compared to commercially available transfection vectors such as polyethylene imine (branched PEI, 25 kDa), partially degraded poly(amido amine) dendrimer (dPAMAM; commercial name: SuperFect (R)) in fibroblasts and adipose tissue derived stem cells (ADSCs). (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:99 / 105
页数:7
相关论文
共 50 条
  • [1] Novel hyperbranched polyethyleneimine conjugate as an efficient non-viral gene delivery vector
    Tae-Hun Kim
    Hye Choi
    Gwang Sig Yu
    Jeil Lee
    Joon Sig Choi
    [J]. Macromolecular Research, 2013, 21 : 1097 - 1104
  • [2] Novel hyperbranched polyethyleneimine conjugate as an efficient non-viral gene delivery vector
    Kim, Tae-Hun
    Choi, Hye
    Yu, Gwang Sig
    Lee, Jeil
    Choi, Joon Sig
    [J]. MACROMOLECULAR RESEARCH, 2013, 21 (10) : 1097 - 1104
  • [3] An efficient, non-viral dendritic vector for gene delivery in tissue engineering
    D P Walsh
    A Heise
    F J O’Brien
    S-A Cryan
    [J]. Gene Therapy, 2017, 24 : 681 - 691
  • [4] An efficient, non-viral dendritic vector for gene delivery in tissue engineering
    Walsh, D. P.
    Heise, A.
    O'Brien, F. J.
    Cryan, S-A
    [J]. GENE THERAPY, 2017, 24 (11) : 681 - 691
  • [5] A non-viral vector for in vivo gene delivery
    Thomas, L
    [J]. LANCET NEUROLOGY, 2005, 4 (10): : 602 - 602
  • [6] An optimized amphiphilic cationic peptide as an efficient non-viral gene delivery vector
    Fominaya, J
    Gasset, M
    García, R
    Roncal, F
    Albar, JP
    Bernad, A
    [J]. JOURNAL OF GENE MEDICINE, 2000, 2 (06): : 455 - 464
  • [7] IONP-PLL: a novel non-viral vector for efficient gene delivery
    Xiang, JJ
    Tang, JQ
    Zhu, SG
    Nie, XM
    Lu, HB
    Shen, SR
    Li, XL
    Tang, K
    Zhou, M
    Li, GY
    [J]. JOURNAL OF GENE MEDICINE, 2003, 5 (09): : 803 - 817
  • [8] Towards effective non-viral gene delivery vector
    Simcikova, Michaela
    Prather, Kristala L. J.
    Prazeres, Duarte M. F.
    Monteiro, Gabriel A.
    [J]. BIOTECHNOLOGY AND GENETIC ENGINEERING REVIEWS, VOL 31, ISSUE 1-2, 2015, 31 (1-2): : 82 - 107
  • [9] Design of head-tail type polycation block copolymer as novel non-viral gene vector
    Harada, Atsushi
    Kawamura, Masanori
    Matsuo, Takashi
    Takahashi, Toshinari
    Kono, Kenji
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2006, 231
  • [10] Progress of cationic gene delivery reagents for non-viral vector
    Ma, Kai
    Mi, Chun-Liu
    Cao, Xiang-Xiang
    Wang, Tian-Yun
    [J]. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2021, 105 (02) : 525 - 538