Simultaneous determination of steroid hormones and pharmaceuticals in killer whale ( Orcinus orca) faecal samples by liquid chromatography tandem mass spectrometry

• Published in: Conservation Physiology
• Main Authors: Ross, Andrew R S, Liao, Xiangjun, Brown, Tanya M
• Other Authors: Hunt, Kathleen, Government of Canada Whales Initiative
• Format: Article in Journal/Newspaper
• Language: English
• Published: Oxford University Press (OUP) 2023
• Subjects: Killer Whale; Orca; Orcinus orca; Killer whale
• Online Access: http://dx.doi.org/10.1093/conphys/coad081; https://academic.oup.com/conphys/article-pdf/11/1/coad081/57312474/coad081.pdf

Abstract We describe a non-invasive method for profiling selected hormones, pharmaceuticals and personal care products (PPCPs) in killer whales (Orcinus orca) based on analysis of faecal samples by liquid chromatography tandem mass spectrometry (LC–MS/MS). The method targets 21 compounds of interest including glucocorticoids, mineralocorticoids, androgens, estrogens, progestogens, selective serotonin uptake inhibitors and an antibacterial/antifungal agent. This method is suitable for routine simultaneous determination of target compounds in killer whale faecal samples as well as validation of immunoassays for the detection and measurement of steroid hormones in faeces. The optimized method involves extraction of freeze-dried faecal material with reagent alcohol and water followed by isolation of the analytes using solid phase extraction with hydrophilic–lipophilic balance cartridges and liquid–liquid extraction with methyl tertiary-butyl ether. Reconstituted extracts were analysed by LC–MS/MS using an electrospray ionization interface. Method limit of quantification ranged from 0.06 to 45.2 ng/g in freeze-dried faecal samples. Except for sertraline, triclosan and estradiol (which was not recovered at the lowest spiked concentration), average intra- and inter-day precisions were within 10%, and average recoveries were between 89.3% and 129.3%, for faecal samples spiked with 5.3, 26.7 or 133 ng/g of each analyte. The method was applied successfully to the analysis of hormones and PPCPs in whale faeces during which 17α-hydroxyprogesterone, a common intermediate in steroid biosynthesis that cross-reacts with precursors and sulphated conjugates in immunoassays, was identified and quantified in all samples.