Nanoparticles disguised as red blood cells to evade the immune system

被引:137
作者
Fang, Ronnie Hongbo
Hu, Che-Ming Jack
Zhang, Liangfang [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept NanoEngn, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
基金
美国国家科学基金会;
关键词
biomimetic nanoparticle; drug delivery; long circulation; red blood cell membrane; DRUG-DELIVERY; PEGYLATION; PROTEIN;
D O I
10.1517/14712598.2012.661710
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The development of nanoparticle platforms with long in vivo circulation half-life has long been one of the major goals in the field of cancer drug delivery. Long-circulating nanoparticles can more effectively localize to the tumor site through either passive or active targeting mechanisms. The current gold standard for bestowing long-circulating attributes involves the use of PEG, which surrounds the particles with a hydration layer and thereby prevents recognition by the mononuclear phagocyte system. Recently, a new strategy for synthesizing biomimetic nanoparticles has been inspired by the body's own long-circulating entities, red blood cells (RBCs). Such a system disguises drug nanocarriers as 'self' using membrane materials directly derived from RBCs. This method has been demonstrated to prolong particle systemic circulation half-life beyond that of the corresponding PEGylated systems. The RBC membrane-coated nanoparticles present a major breakthrough in drug delivery technology and show great promise for clinical applications. Herein we highlight the significance and the unique features of this nature-inspired nanoparticle platform and offer opinions on its future prospects.
引用
收藏
页码:385 / 389
页数:5
相关论文
共 15 条
  • [11] SCHONERMARK S, 1986, J IMMUNOL, V136, P1772
  • [12] Tsai RK, 2010, BLOOD CELL MOL DIS, V45, P67, DOI [10.1016/j.bcmd.2010.02.016, 10.1016/j.hcmd.2010.02.016]
  • [13] PEGylation, successful approach to drug delivery
    Veronese, FM
    Pasut, G
    [J]. DRUG DISCOVERY TODAY, 2005, 10 (21) : 1451 - 1458
  • [14] ISOLATION OF A HUMAN-ERYTHROCYTE MEMBRANE-PROTEIN CAPABLE OF INHIBITING EXPRESSION OF HOMOLOGOUS COMPLEMENT TRANSMEMBRANE CHANNELS
    ZALMAN, LS
    WOOD, LM
    MULLEREBERHARD, HJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (18) : 6975 - 6979
  • [15] Nanoparticles in medicine: Therapeutic applications and developments
    Zhang, L.
    Gu, F. X.
    Chan, J. M.
    Wang, A. Z.
    Langer, R. S.
    Farokhzad, O. C.
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 2008, 83 (05) : 761 - 769