Autor: |
Wharton RE, Ojeda-Torres G, Cunningham B, Feyereisen MC, Hill KL, Abbott NL, Seymour C, Hill D, Lang J, Hamelin EI, Johnson RC |
Jazyk: |
angličtina |
Zdroj: |
Chemical research in toxicology [Chem Res Toxicol] 2018 Sep 17; Vol. 31 (9), pp. 898-903. Date of Electronic Publication: 2018 Sep 05. |
DOI: |
10.1021/acs.chemrestox.8b00126 |
Abstrakt: |
Microcystins are toxins produced by many cyanobacteria species, which are often released into waterways during blue-green algal blooms in freshwater and marine habitats. The consumption of microcystin-contaminated water is a public health concern as these toxins are recognized tumor promoters and are hepatotoxic to humans and animals. A method to confirm human exposures to microcystins is needed; therefore, our laboratory has developed an immunocapture liquid chromatography tandem mass spectrometry (LC-MS/MS) method targeting the conserved adda portion of microcystins for the quantitation of a prevalent and highly toxic congener of microcystin, microcystin-LR (MC-LR). An acute exposure method was initially evaluated for accuracy and precision by analyzing calibrators and quality control (QC) samples ranging from 0.500 to 75.0 ng/mL in urine. All calibrators and QC samples characterized were within 15% of theoretical concentrations. An analysis of acutely exposed mouse urine samples using this method identified MC-LR levels from 10.7 to 33.9 ng/mL. Since human exposures are anticipated to result from low-dose or chronic exposures, a high-sensitivity method was validated with 20 calibration curves and QC samples ranging from 0.0100 to 7.50 ng/mL. Relative standard deviations (RSDs) and inaccuracies of these samples were within 15%, meeting United States Food and Drug Administration (FDA) guidelines for analytical methods, and the limit of detection was 0.00455 ng/mL. In conclusion, we have developed a method which can be used to address public health concerns by precisely and accurately measuring MC-LR in urine samples. |
Databáze: |
MEDLINE |
Externí odkaz: |
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