Carbon nanotubes for delivery of small molecule drugs

被引:470
|
作者
Wong, Bin Sheng [1 ]
Yoong, Sia Lee [2 ]
Jagusiak, Anna [3 ]
Panczyk, Tomasz [4 ]
Ho, Han Kiat [1 ]
Ang, Wee Han [5 ]
Pastorin, Giorgia [1 ,2 ]
机构
[1] Natl Univ Singapore, Dept Pharm, Singapore 117543, Singapore
[2] Natl Univ Singapore, NUS Grad Sch Integrat Sci & Engn NGS, Ctr Life Sci CeLS, Singapore 117456, Singapore
[3] Jagiellonian Univ Med Coll, Chair Med Biochem, PL-31034 Krakow, Poland
[4] Polish Acad Sci, Inst Catalysis & Surface Chem, PL-30239 Krakow, Poland
[5] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
关键词
Carbon nanotubes; Drug delivery; Small molecule drugs; Anticancer drugs; Non-anticancer drugs; PULMONARY TOXICITY ASSESSMENT; ASBESTOS-LIKE PATHOGENICITY; IN-VIVO; TARGETED DELIVERY; CANCER-CELLS; AMPHOTERICIN-B; CONTROLLED-RELEASE; CELLULAR UPTAKE; GALLIC ACID; OSTEOGENIC DIFFERENTIATION;
D O I
10.1016/j.addr.2013.08.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the realm of drug delivery, carbon nanotubes (CNTs) have gained tremendous attention as promising nanocarriers, owing to their distinct characteristics, such as high surface area, enhanced cellular uptake and the possibility to be easily conjugated with many therapeutics, including both small molecules and biologics, displaying superior efficacy, enhanced specificity and diminished side effects. While most CNT-based drug delivery system (DDS) had been engineered to combat cancers, there are also emerging reports that employ CNTs as either the main carrier or adjunct material for the delivery of various non-anticancer drugs. In this review, the delivery of small molecule drugs is expounded, with special attention paid to the current progress of in vitro and in vivo research involving CNT-based DDSs, before finally concluding with some consideration on inevitable complications that hamper successful disease intervention with CNTs. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:1964 / 2015
页数:52
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