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1.
Toxicol Appl Pharmacol ; 278(3): 259-65, 2014 Aug 01.
Artículo en Inglés | MEDLINE | ID: mdl-24823294

RESUMEN

Cobalt exposure is increasing as cobalt demand rises worldwide due to its use in enhancing rechargeable battery efficiency, super-alloys, and magnetic products. Cobalt is considered a possible human carcinogen with the lung being a primary target. However, few studies have considered cobalt-induced toxicity in human lung cells. Therefore, in this study, we sought to determine the cytotoxicity and genotoxicity of particulate and soluble cobalt in human lung cells. Cobalt oxide and cobalt chloride were used as representative particulate and soluble cobalt compounds, respectively. Exposure to both particulate and soluble cobalt induced a concentration-dependent increase in cytotoxicity, genotoxicity, and intracellular cobalt ion levels. Based on intracellular cobalt ion levels, we found that soluble cobalt was more cytotoxic than particulate cobalt while particulate and soluble cobalt induced similar levels of genotoxicity. However, soluble cobalt induced cell cycle arrest indicated by the lack of metaphases at much lower intracellular cobalt concentrations compared to cobalt oxide. Accordingly, we investigated the role of particle internalization in cobalt oxide-induced toxicity and found that particle-cell contact was necessary to induce cytotoxicity and genotoxicity after cobalt exposure. These data indicate that cobalt compounds are cytotoxic and genotoxic to human lung fibroblasts, and solubility plays a key role in cobalt-induced lung toxicity.


Asunto(s)
Carcinógenos Ambientales/toxicidad , Cobalto/toxicidad , Pulmón/efectos de los fármacos , Mutágenos/toxicidad , Transporte Biológico , Carcinógenos Ambientales/análisis , Carcinógenos Ambientales/química , Carcinógenos Ambientales/metabolismo , Ciclo Celular , Línea Celular , Supervivencia Celular/efectos de los fármacos , Células Clonales , Cobalto/análisis , Cobalto/química , Cobalto/metabolismo , Fragmentación del ADN/efectos de los fármacos , Humanos , Pulmón/química , Pulmón/metabolismo , Mutágenos/análisis , Mutágenos/química , Mutágenos/metabolismo , Concentración Osmolar , Óxidos/análisis , Óxidos/química , Óxidos/metabolismo , Óxidos/toxicidad , Tamaño de la Partícula , Fagocitosis/efectos de los fármacos , Solubilidad
2.
ACS Appl Mater Interfaces ; 3(9): 3482-6, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21854025

RESUMEN

There currently exists much debate as to the active state related to the "long afterglow" effect in europium doped oxide materials. Redox couples that consist of Eu(+/2+) and Eu(2+/3+) are discussed, but no common answer is currently accepted. Here, we present a comparison of the optical properties of a commercially available SrAl(2)O(4):Eu, Dy phosphor, as a function of nanoparticle size reduction via dry mechanical milling. X-ray and optical spectroscopic data indicate a significant decrease in phosphorescence efficiency and an increase in laser stimulated emission efficiency as near surface Eu(2+) ions are oxidized to Eu(3+) as a consequence of increased exposure during the milling process. These results show evidence only for Eu(2+/3+) oxidation states, suggesting the mechanism related to long afterglow effect does not arise from Eu(+) species. We also suggest that size reduction, as a rule, cannot be universally applied to improve optical properties of nanostructures.


Asunto(s)
Europio/química , Nanoestructuras/química , Oxidación-Reducción , Óxidos/química , Espectrometría de Fluorescencia , Sincrotrones , Espectroscopía de Absorción de Rayos X
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