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Engineered metal nanoparticles in the sub-nanomolar levels kill cancer cells

BACKGROUND: Small metal nanoparticles obtained from animal blood were observed to be toxic to cultured cancer cells, whereas noncancerous cells were much less affected. In this work, engineered zinc and copper metal nanoparticles were produced from bulk metal rods by an underwater high-voltage disch...

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Autores principales: Vodyanoy, Vitaly, Daniels, Yasmine, Pustovyy, Oleg, MacCrehan, William A, Muramoto, Shin, Stan, Gheorghe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4841435/
https://www.ncbi.nlm.nih.gov/pubmed/27143879
http://dx.doi.org/10.2147/IJN.S101463
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author Vodyanoy, Vitaly
Daniels, Yasmine
Pustovyy, Oleg
MacCrehan, William A
Muramoto, Shin
Stan, Gheorghe
author_facet Vodyanoy, Vitaly
Daniels, Yasmine
Pustovyy, Oleg
MacCrehan, William A
Muramoto, Shin
Stan, Gheorghe
author_sort Vodyanoy, Vitaly
collection PubMed
description BACKGROUND: Small metal nanoparticles obtained from animal blood were observed to be toxic to cultured cancer cells, whereas noncancerous cells were much less affected. In this work, engineered zinc and copper metal nanoparticles were produced from bulk metal rods by an underwater high-voltage discharge method. The metal nanoparticles were characterized by atomic force microscopy and X-ray photoelectron spectroscopy. The metal nanoparticles, with estimated diameters of 1 nm–2 nm, were determined to be more than 85% nonoxidized. A cell viability assay and high-resolution light microscopy showed that exposure of RG2, cultured rat brain glioma cancer cells, to the zinc and copper nanoparticles resulted in cell morphological changes, including decreased cell adherence, shrinking/rounding, nuclear condensation, and budding from cell bodies. The metal-induced cell injuries were similar to the effects of staurosporine, an active apoptotic reagent. The viability experiments conducted for zinc and copper yielded values of dissociation constants of 0.22±0.08 nmol/L (standard error [SE]) and 0.12±0.02 nmol/L (SE), respectively. The noncancerous astrocytes were not affected at the same conditions. Because metal nanoparticles were lethal to the cancer cells at sub-nanomolar concentrations, they are potentially important as nanomedicine. PURPOSE: Lethal concentrations of synthetic metal nanoparticles reported in the literature are a few orders of magnitude higher than the natural, blood-isolated metal nanoparticles; therefore, in this work, engineered metal nanoparticles were examined to mimic the properties of endogenous metal nanoparticles. MATERIALS AND METHODS: RG2, rat brain glioma cells CTX TNA2 brain rat astrocytes, obtained from the American Type Culture Collection, high-voltage discharge, atomic force microscope, X-ray photoelectron spectroscopy, high-resolution light microscopy, zeta potential measurements, and 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) assay were used in this work. RESULTS: Engineered zinc and copper metal nanoparticles of size 1 nm–2 nm were lethal to cultured RG2 glioma cancer cells. Cell death was confirmed by MTT assay, showing that the relative viability of RG2 glioma cells is reduced in a dose-dependent manner at sub-nanomolar concentrations of the nanoparticles. The noncancerous astrocytes were not affected at the same conditions. CONCLUSION: The engineered and characterized zinc and copper nanoparticles are potentially significant as biomedicine.
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spelling pubmed-48414352016-05-03 Engineered metal nanoparticles in the sub-nanomolar levels kill cancer cells Vodyanoy, Vitaly Daniels, Yasmine Pustovyy, Oleg MacCrehan, William A Muramoto, Shin Stan, Gheorghe Int J Nanomedicine Original Research BACKGROUND: Small metal nanoparticles obtained from animal blood were observed to be toxic to cultured cancer cells, whereas noncancerous cells were much less affected. In this work, engineered zinc and copper metal nanoparticles were produced from bulk metal rods by an underwater high-voltage discharge method. The metal nanoparticles were characterized by atomic force microscopy and X-ray photoelectron spectroscopy. The metal nanoparticles, with estimated diameters of 1 nm–2 nm, were determined to be more than 85% nonoxidized. A cell viability assay and high-resolution light microscopy showed that exposure of RG2, cultured rat brain glioma cancer cells, to the zinc and copper nanoparticles resulted in cell morphological changes, including decreased cell adherence, shrinking/rounding, nuclear condensation, and budding from cell bodies. The metal-induced cell injuries were similar to the effects of staurosporine, an active apoptotic reagent. The viability experiments conducted for zinc and copper yielded values of dissociation constants of 0.22±0.08 nmol/L (standard error [SE]) and 0.12±0.02 nmol/L (SE), respectively. The noncancerous astrocytes were not affected at the same conditions. Because metal nanoparticles were lethal to the cancer cells at sub-nanomolar concentrations, they are potentially important as nanomedicine. PURPOSE: Lethal concentrations of synthetic metal nanoparticles reported in the literature are a few orders of magnitude higher than the natural, blood-isolated metal nanoparticles; therefore, in this work, engineered metal nanoparticles were examined to mimic the properties of endogenous metal nanoparticles. MATERIALS AND METHODS: RG2, rat brain glioma cells CTX TNA2 brain rat astrocytes, obtained from the American Type Culture Collection, high-voltage discharge, atomic force microscope, X-ray photoelectron spectroscopy, high-resolution light microscopy, zeta potential measurements, and 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) assay were used in this work. RESULTS: Engineered zinc and copper metal nanoparticles of size 1 nm–2 nm were lethal to cultured RG2 glioma cancer cells. Cell death was confirmed by MTT assay, showing that the relative viability of RG2 glioma cells is reduced in a dose-dependent manner at sub-nanomolar concentrations of the nanoparticles. The noncancerous astrocytes were not affected at the same conditions. CONCLUSION: The engineered and characterized zinc and copper nanoparticles are potentially significant as biomedicine. Dove Medical Press 2016-04-18 /pmc/articles/PMC4841435/ /pubmed/27143879 http://dx.doi.org/10.2147/IJN.S101463 Text en © 2016 Vodyanoy et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Vodyanoy, Vitaly
Daniels, Yasmine
Pustovyy, Oleg
MacCrehan, William A
Muramoto, Shin
Stan, Gheorghe
Engineered metal nanoparticles in the sub-nanomolar levels kill cancer cells
title Engineered metal nanoparticles in the sub-nanomolar levels kill cancer cells
title_full Engineered metal nanoparticles in the sub-nanomolar levels kill cancer cells
title_fullStr Engineered metal nanoparticles in the sub-nanomolar levels kill cancer cells
title_full_unstemmed Engineered metal nanoparticles in the sub-nanomolar levels kill cancer cells
title_short Engineered metal nanoparticles in the sub-nanomolar levels kill cancer cells
title_sort engineered metal nanoparticles in the sub-nanomolar levels kill cancer cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4841435/
https://www.ncbi.nlm.nih.gov/pubmed/27143879
http://dx.doi.org/10.2147/IJN.S101463
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