Cell-penetrating CNTs for delivery of therapeutics

被引:209
作者
Lacerda, Lara [1 ]
Raffa, Simona [2 ]
Prato, Maurizio [3 ]
Bianco, Alberto [4 ]
Kostarelos, Kostas [1 ]
机构
[1] Univ London, Sch Pharm, Ctr Drug Delivery Res, Nanomed Lab, London WC1N 1AX, England
[2] Scuola Super Sants Anna, CRIM Res Ctr Microenge, I-56025 Pontedera, Italy
[3] CNRS, Inst Biol Mol & Cellulaire, Lab Immunol & Chim Therapeut, F-67084 Strasbourg, France
[4] Univ Trieste, Dipartimento Sci Farmaceut, I-34127 Trieste, Italy
关键词
D O I
10.1016/S1748-0132(07)70172-X
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The use of carbon-based nanostructures, such as carbon nanotubes, in biomedicine is increasingly attracting attention. One key advantage of carbon nanotubes is their ability to translocate through plasma membranes, allowing their use for the delivery of therapeutically active molecules in a manner that resembles cell-penetrating peptides. Moreover, exploitation of their unique electrical, optical, thermal, and spectroscopic properties in a biological context is hoped to yield great advances in the detection, monitoring, and therapy of disease. Here we offer a speculative overview of the general principles behind the mechanism of carbon nanotube penetration of the plasma membrane and a snapshot of the different therapeutic modalities based on these fascinating nanostructures that are currently being investigated.
引用
收藏
页码:38 / 43
页数:6
相关论文
共 29 条
[1]   Cationic carbon nanotubes bind to CpG oligodeoxynucleotides and enhance their immunostimulatory properties [J].
Bianco, A ;
Hoebeke, J ;
Godefroy, S ;
Chaloin, O ;
Pantarotto, D ;
Briand, JP ;
Muller, S ;
Prato, M ;
Partidos, CD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (01) :58-59
[2]   Highly efficient molecular delivery into mammalian cells using carbon nanotube spearing [J].
Cai, D ;
Mataraza, JM ;
Qin, ZH ;
Huang, ZP ;
Huang, JY ;
Chiles, TC ;
Carnahan, D ;
Kempa, K ;
Ren, ZF .
NATURE METHODS, 2005, 2 (06) :449-454
[3]   Near-infrared fluorescence microscopy of single-walled carbon nanotubes in phagocytic cells [J].
Cherukuri, P ;
Bachilo, SM ;
Litovsky, SH ;
Weisman, RB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (48) :15638-15639
[4]   Soluble single-walled carbon nanotubes as longboat delivery systems for Platinum(IV) anticancer drug design [J].
Feazell, Rodney P. ;
Nakayama-Ratchford, Nozomi ;
Dai, Hongjie ;
Lippard, Stephen J. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (27) :8438-+
[5]   Mechanics of receptor-mediated endocytosis [J].
Gao, HJ ;
Shi, WD ;
Freund, LB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (27) :9469-9474
[6]   Carbon nanotube delivery of the GFP gene into mammalian cells [J].
Gao, LZ ;
Nie, L ;
Wang, TH ;
Qin, YJ ;
Guo, ZX ;
Yang, DL ;
Yan, XY .
CHEMBIOCHEM, 2006, 7 (02) :239-242
[7]   Organic functionalization of carbon nanotubes [J].
Georgakilas, V ;
Kordatos, K ;
Prato, M ;
Guldi, DM ;
Holzinger, M ;
Hirsch, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (05) :760-761
[8]   Single-walled carbon nanotube spectroscopy in live cells: Towards long-term labels and optical sensors [J].
Heller, DA ;
Baik, S ;
Eurell, TE ;
Strano, MS .
ADVANCED MATERIALS, 2005, 17 (23) :2793-+
[9]   Carbon nanotubes as intracellular transporters for proteins and DNA: An investigation of the uptake mechanism and pathway [J].
Kam, NWS ;
Liu, ZA ;
Dai, HJ .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (04) :577-581
[10]   Functionalization of carbon nanotubes via cleavable disulfide bonds for efficient intracellular delivery of siRNA and potent gene silencing [J].
Kam, NWS ;
Liu, Z ;
Dai, HJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (36) :12492-12493