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Manganese (Mn) is an essential nutrient for metabolic functions, yet excessive exposure can lead to neurological disease in adults and neurodevelopmental deficits in children. Drinking water represents one of the routes of excessive Mn exposure. Both natural enrichment from rocks and soil, and man-made contamination can pollute groundwater that supplies drinking water for a substantial fraction of the U.S. population. Conventional methods for Mn monitoring in drinking water are costly and involve a long turn-around time. Recent advancements in electrochemical sensing, however, have led to the development of miniature sensors for Mn determination. These sensors rely on a cathodic stripping voltammetry electroanalytical technique on a miniaturized platinum working electrode. In this study, we validate these electrochemical sensors for the determination of Mn concentrations in drinking water against the standard method using inductively coupled plasma mass spectrometry (ICP-MS). Drinking water samples (n = 78) in the 0.03 ppb to 5.3 ppm range were analyzed. Comparisons with ICP-MS yielded 100% agreement, ∼70% accuracy, and ∼91% precision. We envision the use of our system for rapid and inexpensive point-of-use identification of Mn levels in drinking water, which is especially valuable for frequent monitoring where contamination is present.
Boselli et al. (Wed,) studied this question.