Triple functionalisation of single-walled carbon nanotubes with doxorubicin, a monoclonal antibody, and a fluorescent marker for targeted cancer therapy

被引:199
作者
Heister, Elena [1 ,4 ]
Neves, Vera [1 ,4 ]
Tilmaciu, Carmen [2 ]
Lipert, Kamil [3 ]
Beltran, Vanesa Sanz [1 ,4 ]
Coley, Helen M. [1 ]
Silva, S. Ravi P. [4 ]
McFadden, Johnjoe [1 ]
机构
[1] Univ Surrey, Fac Hlth & Med Sci, Guildford GU2 7XH, Surrey, England
[2] Univ Toulouse 3, CNRS, UMR 5085, CIRIMAT LCMIE, F-31077 Toulouse 9, France
[3] Leibniz Inst Solid State & Mat Res IFW, D-01069 Dresden, Germany
[4] Univ Surrey, Adv Technol Inst, Nanoelect Ctr, Guildford GU2 7XH, Surrey, England
关键词
OXIDATION; ACID; TEMPERATURE; AGENTS;
D O I
10.1016/j.carbon.2009.03.057
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Single-walled carbon nanotubes (SWCNTs) have been identified as a transporter for anticancer drugs, as they are capable of penetrating mammalian cell membranes and allow for a high drug loading due to their nanoscale dimensions and high aspect ratio. In addition, they can assist the targeting of therapeutic agents to the desired site of action by conjugation to antibodies or ligands of cancer cell surface receptors, which increases the effectiveness of the treatment and reduces side effects. In this work, we present a method for the triple functionalisation of oxidised SWCNTs with the anti-cancer drug doxorubicin, a monoclonal antibody, and a fluorescent marker at non-competing binding sites. The proposed methodology allows for the targeted delivery of the anti-cancer drug to cancer cells and the visualisation of the cellular uptake of SWCNTs by confocal microscopy. We show that the complex is efficiently taken up by cancer cells with subsequent intracellular release of doxorubicin, which then translocates to the nucleus while the nanotubes remain in the cytoplasm. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2152 / 2160
页数:9
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