期刊论文详细信息
Sensors
Cytotoxicity Investigation on Cultured Human Blood Cells Treated with Single-Wall Carbon Nanotubes
Olga Zeni3  Rosanna Palumbo1  Romeo Bernini3  Luigi Zeni2  Maurizio Sarti3 
[1] Istituto di Biostrutture e Bioimmagini (IBB) – CNR, Via Mezzocannone, 16, 80137 Napoli, Italy;Seconda Università degli Studi di Napoli, Dipartimento di Ingegneria dell' Informazione (DII), Aversa, Italy;Istituto per il Rilevamento Elettromagnetico dell'Ambiente (IREA) - CNR, Via Diocleziano, 328, 80124 Napoli, Italy
关键词: Human blood cells;    carbon nanotubes;    cytotoxicity;    metabolic activity;   
DOI  :  10.3390/s8010488
来源: mdpi
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【 摘 要 】

The single-wall carbon nanotubes (SWCNTs) are one of the new materials of emerging technologies. They are becoming increasingly studied for the possible applications in electronics, optics and biology. In particular, very promising fields of application are the development of optical biosensors and the intracellular drug delivery. Nevertheless, there is a paucity of information on their toxicological properties and on potential human health risk. In the present study the SWCNTs were investigated for the possible induction of toxicity in human blood cells. Cell growth, viability, apoptosis and metabolic activity were evaluated in proliferating human peripheral blood lymphocytes. In un-stimulated human leukocytes primary DNA damage was also evaluated. SWCNTs concentrations ranging from 1 to 50 μg/ml were tested, and treatment duration varied from 6 to 72 h, in accordance with the biological target investigated. A statistically significant decrease in cell growth was found in cells treated with the highest concentrations (25 and 50 μg/ml). Such decrease was not associated to cell death or apoptosis, but it was demonstrated to be related to a decrease in metabolic activity, as assessed by resazurin assay. Moreover, treatments of 6 h with SWCNTs concentrations of 1, 5 and 10 μg/ml failed to induce primary DNA damage on the entire human leukocytes population.

【 授权许可】

Unknown   
© 2008 by MDPI

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