Delivery of drugs and biomolecules using carbon nanotubes

被引:227
作者
Vashist, Sandeep Kumar [1 ,2 ]
Zheng, Dan [2 ,3 ]
Pastorin, Giorgia [4 ]
Al-Rubeaan, Khalid [5 ]
Luong, John H. T. [6 ,7 ]
Sheu, Fwu-Shan [1 ,2 ]
机构
[1] Natl Univ Singapore, Dept Elect & Comp Engn, Singapore 117576, Singapore
[2] Natl Univ Singapore, NUSNNI NanoCore, Singapore 117580, Singapore
[3] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
[4] Natl Univ Singapore, Dept Pharm, Singapore 117543, Singapore
[5] King Saud Univ, Univ Diabet Ctr, Riyadh 11415, Saudi Arabia
[6] Natl Res Council Canada, Biotechnol Res Inst, Montreal, PQ H4P 2R2, Canada
[7] Univ Coll Cork, Dept Chem, Cork, Ireland
关键词
LIPOSOME-ENCAPSULATED DOXORUBICIN; SMALL INTERFERING RNA; IN-VITRO; MAMMALIAN-CELLS; CANCER-CELLS; INTRACELLULAR DELIVERY; MAGNETIC NANOPARTICLES; RHEUMATOID-ARTHRITIS; PULMONARY TOXICITY; RAMAN-SPECTROSCOPY;
D O I
10.1016/j.carbon.2011.05.049
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
Carbon nanotubes (CNTs) have emerged as one of the most advanced nanovectors for the highly efficient delivery of drugs and biomolecules. They offer several appealing features such as large surface areas with well defined physico-chemical properties as well as unique optical and electrical properties. They can be conjugated non-covalently or covalently with drugs, biomolecules and nanoparticles. Albeit some pending concerns about their toxicity in vitro and in vivo, functionalized CNTs appear to exhibit very low toxicity and are not immunogenic. Thus, they could be promising carriers with a great potential for the development of a new-generation delivery system for drugs and biomolecules. There have been significant advances in the field of CNT-based drug delivery, especially in the specific targeting of anticancer and anti-inflammatory drugs for tissues and organs in the body, where their therapeutic effect is highly required. Other promising applications are the delivery of DNA, RNA and proteins. Crown Copyright (C) 2011 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:4077 / 4097
页数:21
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