| Literature DB >> 34898679 |
James M Harrington1, Laura G Haines1, Amal S Essader1, Chamindu Liyanapatirana1, Eric A Poitras1, Frank X Weber1, Keith E Levine1, Reshan A Fernando1, Veronica G Robinson2, Suramya Waidyanatha2.
Abstract
Human exposure to vanadium (V) is anticipated because it is a drinking water contaminant. Due to limited data on soluble V salts, the National Toxicology Program is investigating the toxicity in rodents following drinking water exposure. Measurement of internal V dose allows for interpretation of toxicology data. The objective of this study was to develop and validate an inductively coupled plasma-mass spectrometric method to quantitate total V in rat plasma. The method was linear (r ≥ 0.99) from 5.00 - 1,000 ng V/mL. Intra- and inter-day relative error (% RE) and relative standard deviation (% RSD) of spiked plasma samples were 8.5% - 15.6% RE and ≤ 1.8% RSD and 7.3% - 11.7% RE and ≤ 3.1% RSD, respectively. The limit of detection was 0.268 ng V/mL plasma and absolute percent recovery was 113%. Standards up to 7,500 ng V/mL plasma were diluted into the validated range (5.6% RE, 0.9% RSD). V in extracted plasma samples over 15 days at ambient and refrigerated conditions was from 97.7 - 126% of day 0. Determined plasma V concentrations after three freeze-thaw cycles and after frozen storage for up to 63 days ranged from 100 - 106% and 100 - 122% of day 0, respectively. The method was extended to rat urine (accuracy and precision -2.0 - 0.3% RE and <0.6% RSD, respectively for same linear range). These data demonstrate that the method is suitable to quantitate V in rat plasma and urine.Entities:
Keywords: Vanadium; bioanalytical; method validation; rat plasma; rat urine
Year: 2021 PMID: 34898679 PMCID: PMC8659411 DOI: 10.1080/00032719.2021.1890107
Source DB: PubMed Journal: Anal Lett ISSN: 0003-2719 Impact factor: 2.329