Open Access. Powered by Scholars. Published by Universities.®

Environmental Health Commons

Open Access. Powered by Scholars. Published by Universities.®

Medicine and Health Sciences

Series

Cytotoxicity

Articles 1 - 2 of 2

Full-Text Articles in Environmental Health

Hexavalent Chromium-Induced Cytotoxicity And Mutagenicity: A Study Of Protection By Ascorbic Acid And Epigallocatechin Gallate, Timothy P. Mayotte Jul 2019

Hexavalent Chromium-Induced Cytotoxicity And Mutagenicity: A Study Of Protection By Ascorbic Acid And Epigallocatechin Gallate, Timothy P. Mayotte

Honors Program Projects

Hexavalent chromium, or Cr(VI), is a potent oxidizer and known carcinogen, that is found at varying levels in the water sources of more than 200 million Americans. However, the exact mechanism of carcinogenicity remains unknown, and though the government currently regulates total chromium levels, they have yet to determine a permissible exposure limit for Cr(VI). Moreover, there is currently no preventative treatment for Cr(VI). Because of Cr(VI)’s strong oxidative power, we hypothesized that it causes DNA mutation and cell death via oxidation and that antioxidants could prevent this from occurring. To test this, we first assessed the viability of human …


Toxicity Of Engineered Nanomaterials And Their Transformation Products Following Wastewater Treatment On A549 Human Lung Epithelial Cells, Yanjun Ma, Subbiah Elankumaran, Linsey C. Marr, Eric P. Vejerano, Amy Pruden Sep 2014

Toxicity Of Engineered Nanomaterials And Their Transformation Products Following Wastewater Treatment On A549 Human Lung Epithelial Cells, Yanjun Ma, Subbiah Elankumaran, Linsey C. Marr, Eric P. Vejerano, Amy Pruden

Faculty Publications

Here we characterize the toxicity of environmentally-relevant forms of engineered nanomaterials (ENMs), which can transform during wastewater treatment and persist in aqueous effluents and biosolids. In an aerosol exposure scenario, cytotoxicity and genotoxicity of effluents and biosolids from lab-scale sequencing batch reactors (SBRs) to A549 human lung epithelial cells were examined. The SBRs were dosed with nanoAg, nano zero-valent iron (NZVI), nanoTiO2 and nanoCeO2 at sequentially increasing concentrations from 0.1 to 20 mg/L. Toxicities were compared to outputs from SBRs dosed with ionic/bulk analogs, undosed SBRs, and pristine ENMs. Pristine nanoAg and NZVI showed significant cytotoxicity to A549 cells in …