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ZnO, TiO(2), SiO(2,) and Al(2)O(3) nanoparticles-induced toxic effects on human fetal lung fibroblasts / 生物医学与环境科学(英文)
Biomedical and Environmental Sciences ; (12): 661-669, 2011.
Artigo em Inglês | WPRIM | ID: wpr-235584
ABSTRACT
<p><b>OBJECTIVE</b>This study aims to investigate and compare the toxic effects of four types of metal oxide (ZnO, TiO(2), SiO(2,) and Al(2)O(3)) nanoparticles with similar primary size (∼20 nm) on human fetal lung fibroblasts (HFL1) in vitro.</p><p><b>METHODS</b>The HFL1 cells were exposed to the nanoparticles, and toxic effects were analyzed by using MTT assay, cellular morphology observation and Hoechst 33 258 staining.</p><p><b>RESULTS</b>The results show that the four types of metal oxide nanoparticles lead to cellular mitochondrial dysfunction, morphological modifications and apoptosis at the concentration range of 0.25-1.50 mg/mL and the toxic effects are obviously displayed in dose-dependent manner. ZnO is the most toxic nanomaterials followed by TiO(2), SiO(2), and Al(2)O(3) nanoparticles in a descending order.</p><p><b>CONCLUSION</b>The results highlight the differential cytotoxicity associated with exposure to ZnO, TiO(2), SiO(2), and Al(2)O(3) nanoparticles, and suggest an extreme attention to safety utilization of these nanomaterials.</p>
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Patologia / Propriedades de Superfície / Titânio / Óxido de Zinco / Linhagem Celular / Sobrevivência Celular / Química / Embriologia / Microscopia de Contraste de Fase / Apoptose Limite: Humanos Idioma: Inglês Revista: Biomedical and Environmental Sciences Ano de publicação: 2011 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Patologia / Propriedades de Superfície / Titânio / Óxido de Zinco / Linhagem Celular / Sobrevivência Celular / Química / Embriologia / Microscopia de Contraste de Fase / Apoptose Limite: Humanos Idioma: Inglês Revista: Biomedical and Environmental Sciences Ano de publicação: 2011 Tipo de documento: Artigo