Research Article

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2018, 11(4): 2204–2216

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https://doi.org/10.1007/s12274-017-1838-2

Selective toxicity of hydroxyl-rich carbon nanodots for cancer research

Tak H. Kim1, Joseph P. Sirdaarta2, Qian Zhang3, Ehsan Eftekhari1, James St. John3,4, Derek Kennedy3, Ian E. Cock2, and Qin Li1 (*)

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1 Queensland Micro and Nano Technology Center & School of Engineering, Griffith University, 170 Kessels Rd, Nathan QLD 4111, Australia
2 Australian Rivers Institute & School of Natural Sciences, Griffith University, 170 Kessels Rd, Nathan QLD 4111, Australia
3 Griffith Institute for Drug Discovery, Griffith University, 46 Don Young Rd, Nathan QLD 4111, Australia
4 Menzies Health Institute Queensland, Griffith University, Parkland Drive, Southport QLD 4222, Australia

Keywords: carbon nanodots, nanotoxicity, fluorescence, choriocarcinoma cells, thioredoxin reductase
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ABSTRACT The toxicity of nanoparticles in a biological system is an integration of effects arising from surface functionality, particle size, ionic dissolution, etc. This complexity suggests that generalization of a material’s toxicity may be inappropriate. Moreover, from a medicinal point of view, toxicity can be used for treatment of malignant cells, such as cancer. In this study, highly biocompatible carbon nanodots (gCDs) were synthesized by reacting citric acid and urea in glycerol, which resulted in abundant hydroxyl functional groups on the particle surface. gCDs show excitation-dependent photoluminescence but with bright green to yellow emission. Importantly, a series of toxicity assessments showed that as-synthesized gCDs possessed exceptional biocompatibilities to various biological entities including 18 bacteria species, Petunia axillaris seedlings, and Artemia franciscana nauplii. Furthermore, the particles were shown to have low to no toxic effects on human embryonic kidney (HEK-293), breast (MCF-7), and oral squamous (CAL-27) carcinoma cell lines. Of particular interest, the gCDs displayed antiproliferative activities against ovarian choriocarcinoma cells (JAr/Jeg-3 cell lines), which may be further explored for cancer drug discovery.
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Selective toxicity of hydroxyl-rich carbon nanodots for cancer research. Nano Res. 2018, 11(4): 2204–2216 https://doi.org/10.1007/s12274-017-1838-2

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