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1.
Toxicol Ind Health ; 39(1): 23-35, 2023 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-36433804

RESUMO

Airborne crystalline silica (SiO2) particles are one of the most common pollutants in stone industries. Limited studies have investigated the health effects of crystalline SiO2 nanoparticles. Hence, the objective of this study was to study the cytotoxicity of SiO2 in nano and micron sizes. A mineral quartz sample in the range of 0.2-0.8 mm sizes was purchased. These particles were ground at about 5 and 0.1 microns. Human cell line A549 was exposed to micro and nanometer particles at concentrations of 10, 50, 100, and 250 µg/ml for 24 and 72 h. Subsequently, the cytotoxicity of exposed cells was investigated by measuring cell survival, ROS generation, mitochondrial permeability, and intracellular glutathione content. The results showed that crystalline SiO2 nano and microparticles decreased cell survival, increased ROS generation, damaged the mitochondrial membrane, and lowered the antioxidant content of these cells in a concentration- and time-dependent manner. The toxicity of crystalline SiO2 microparticles at concentrations ≤50 µg/mL was greater than for nanoparticles, which was the opposite at concentrations ≥100 µg/mL. Exposure time and concentration were crucial factors for the cytotoxicity of exposed A549 cells to crystalline SiO2 particles, which can affect the severity of the effect of particle size. Due to the limitation of exposure concentration and test durations in this study, further studies on the parameters of nanoparticle toxicity and underlying mechanisms could advance our knowledge.


Assuntos
Nanopartículas , Dióxido de Silício , Humanos , Dióxido de Silício/toxicidade , Espécies Reativas de Oxigênio/metabolismo , Linhagem Celular , Tamanho da Partícula , Nanopartículas/toxicidade , Pulmão , Sobrevivência Celular
2.
Asian Pac J Cancer Prev ; 22(2): 325-332, 2021 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-33639644

RESUMO

INTRODUCTION: Amorphous silicon dioxide (A-SiO2) is abundant in the Earth's crust, the A-SiO2 nano and microparticles are released into the air through industrial and manufacturing activities. Due to the limited available toxicological information, the objective of the present study was to evaluate the toxicity of different sizes of A-SiO2 particles on the A549 cell-lines in an in vitro study. MATERIALS AND METHODS: The A-SiO2 particles in two categories of nano (10-100 nm) and micro (< 5um) were used in this study. The human lung A549 cell-line was exposed to either nano- or micro-sized A-SiO2 particles at 10, 50, 100, and 250 µg/ml, and the effects were investigated. RESULTS: The cytotoxicity of A-SiO2 nano and microparticles in both 24- and 72-hour exposure times resulted in decreased cell survival, mitochondrial membrane potential, and increased ROS generation which was concentration-time dependent (P <0.05) but glutathione content was not affected in a time-dependent manner. Cytotoxicity of nanoparticles, contrary to the previous study, was not higher than microparticles in the comparable dose and exposure times. CONCLUSION: The rate of ROS generation in the A549 cell-line exposed to A-SiO2 nanoparticles was higher than microparticles. And at the same time, cell survival for exposed cells to A-SiO2 nano and microparticles were higher for nanoparticles in shorter exposure periods and was inversely concentration- and time-dependent. Further studies on exploring the effect of size and its possible toxic mechanism are recommended to achieve a more credible risk assessment.


Assuntos
Sobrevivência Celular/efeitos dos fármacos , Pulmão/efeitos dos fármacos , Pulmão/patologia , Tamanho da Partícula , Dióxido de Silício/farmacologia , Células A549 , Técnicas de Cultura de Células , Glutationa/metabolismo , Humanos , Pulmão/metabolismo , Potencial da Membrana Mitocondrial/efeitos dos fármacos , Nanopartículas , Espécies Reativas de Oxigênio/metabolismo
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