Precipitation of aqueous transition metals in particulate matter during the dithiothreitol (DTT) oxidative potential assay
Precipitation of aqueous transition metals in particulate matter during the dithiothreitol (DTT) oxidative potential assay
复制标题
二硫苏糖醇 (DTT) 氧化电位测定过程中颗粒物中水性过渡金属的沉淀
DOI:
10.1039/d2em00005a
复制
发表时间:
2022
期刊:
影响因子:
--
通讯作者:
Reed, Brian E.
中科院分区:
文献类型:
--
作者:
Yalamanchili, Jayashree;Hennigan, Christopher J.;Reed, Brian E.
Transition metals in particulate matter (PM) are hypothesized to have enhanced toxicity based on their oxidative potential (OP). The acellular dithiothreitol (DTT) assay is widely used to measure the OP of PM and its chemical components. In our prior study, we showed that the DTT assay (pH 7.4, 0.1 M phosphate buffer, 37 °C) provides favorable thermodynamic conditions for precipitation of multiple metals present in PM. This study utilizes multiple techniques to characterize the precipitation of aqueous metals present at low concentrations in the DTT assay. Metal precipitation was identified using laser particle light scattering analysis, direct chemical measurement of aqueous metal removal, and microscopic imaging. Experiments were run with aqueous metals from individual metal salts and a well-characterized urban PM standard (NIST SRM-1648a, Urban Particulate Matter). Our results demonstrated rapid precipitation of metals in the DTT assay. Metal precipitation was independent of DTT but dependent on metal concentration. Metal removal in the chemically complex urban PM samples exceeded the thermodynamic predictions and removal seen in single metal salt experiments, suggesting co-precipitation and/or adsorption may have occurred. These results have broad implications for other acellular assays that study PM metals using phosphate buffer, and subsequently, the PM toxicity inferred from these assays.