Are diamond nanoparticles cytotoxic?

被引:576
作者
Schrand, Amanda M.
Huang, Houjin
Carlson, Cataleya
Schlager, John J.
Osawa, Eiji
Hussain, Saber M.
Dai, Liming
机构
[1] Univ Dayton, Dept Chem & Mat Engn, Dayton, OH 45469 USA
[2] USAF, Res Lab, Appl Biotechnol Branch, Human Effectiveness Directorate, Wright Patterson AFB, OH 45433 USA
[3] NanoCarbon Res Inst Ltd, Chiba 2770882, Japan
关键词
D O I
10.1021/jp066387v
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
Finely divided carbon particles, including charcoal, lampblack, and diamond particles, have been used for ornamental and official tattoos since ancient times. With the recent development in nanoscience and nanotechnology, carbon-based nanomaterials (e.g., fullerenes, nanotubes, nanodiamonds) attract a great deal of interest. Owing to their low chemical reactivity and unique physical properties, nanodiamonds could be useful in a variety of biological applications such as carriers for drugs, genes, or proteins; novel imaging techniques; coatings for implantable materials; and biosensors and biomedical nanorobots. Therefore, it is essential to ascertain the possible hazards of nanodiamonds to humans and other biological systems. We have, for the first time, assessed the cytotoxicity of nanodiamonds ranging in size from 2 to 10 nm. Assays of cell viability such as mitochondrial function (MTT) and luminescent ATP production showed that nanodiamonds were not toxic to a variety of cell types. Furthermore, nanodiamonds did not produce significant reactive oxygen species. Cells can grow on nanodiamond-coated substrates without morphological changes compared to controls. These results suggest that nanodiamonds could be ideal for many biological applications in a diverse range of cell types.
引用
收藏
页码:2 / 7
页数:6
相关论文
共 42 条
[21]   Functionalized carbon nanotubes and nanodiamonds for engineering and biomedical applications [J].
Khabashesku, VN ;
Margrave, JL ;
Barrera, EV .
DIAMOND AND RELATED MATERIALS, 2005, 14 (3-7) :859-866
[22]   Carbon nanotube-mediated delivery of peptides and genes to cells: translating nanobiotechnology to therapeutics [J].
Kostarelos, K ;
Lacerda, L ;
Partidos, CD ;
Prato, M ;
Blanco, A .
JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2005, 15 (01) :41-47
[23]   Unusually tight aggregation in detonation nanodiamond:: Identification and disintegration [J].
Krüger, A ;
Kataoka, F ;
Ozawa, M ;
Fujino, T ;
Suzuki, Y ;
Aleksenskii, AE ;
Vul', AY ;
Osawa, E .
CARBON, 2005, 43 (08) :1722-1730
[24]  
Loft S, 1999, METHOD ENZYMOL, V300, P166
[25]   Single-walled carbon nanotube induces oxidative stress and activates nuclear transcription factor-κB in human keratinocytes [J].
Manna, SK ;
Sarkar, S ;
Barr, J ;
Wise, K ;
Barrera, EV ;
Jejelowo, O ;
Rice-Ficht, AC ;
Ramesh, GT .
NANO LETTERS, 2005, 5 (09) :1676-1684
[26]   Multi-walled carbon nanotube interactions with human epidermal keratinocytes [J].
Monteiro-Riviere, NA ;
Nemanich, RJ ;
Inman, AO ;
Wang, YYY ;
Riviere, JE .
TOXICOLOGY LETTERS, 2005, 155 (03) :377-384
[27]   Respiratory toxicity of multi-wall carbon nanotubes [J].
Muller, J ;
Huaux, F ;
Moreau, N ;
Misson, P ;
Heilier, JF ;
Delos, M ;
Arras, M ;
Fonseca, A ;
Nagy, JB ;
Lison, D .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2005, 207 (03) :221-231
[28]   Toxic potential of materials at the nanolevel [J].
Nel, A ;
Xia, T ;
Mädler, L ;
Li, N .
SCIENCE, 2006, 311 (5761) :622-627
[29]   Control of sp2/sp3 carbon ratio and surface chemistry of nanodiamond powders by selective oxidation in air [J].
Osswald, Sebastian ;
Yushin, Gleb ;
Mochalin, Vadym ;
Kucheyev, Sergei O. ;
Gogotsi, Yury .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (35) :11635-11642
[30]   Translocation of bioactive peptides across cell membranes by carbon nanotubes [J].
Pantarotto, D ;
Briand, JP ;
Prato, M ;
Bianco, A .
CHEMICAL COMMUNICATIONS, 2004, (01) :16-17