• Erandi Hewawasam, Ge Liu, David W Jeffery, Beverly S Muhlhausler, and Robert A Gibson.
• Food and Nutrition Research Group, Department of Wine and Food Science, School of Agriculture, Food and Wine, The University of Adelaide, PMB 1, Glen Osmond, South Australia 5064, Australia; Healthy Mothers, Babies and Children, South Australian Health and Medical Research Institute, North Terrace, Adelaide 5000, Australia.
• Prostaglandins Leukot. Essent. Fatty Acids. 2018 Oct 1; 137: 12-18.

AbstractOxylipins are biologically important lipid mediators that are derived enzymatically from polyunsaturated fatty acids (PUFA) and have a major role in regulating inflammatory processes. The currently available methods for measuring oxylipins from human biological samples have limitations, which restricts their use in large studies. We have developed a novel method for measuring 21 oxylipins from dried blood spot (DBS) using ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) and stable isotope dilution analysis. Our new method is reproducible and precise and enables the high throughput analysis and quantitation of bioactive oxylipins in small volumes of blood. In the future, this new method can be readily applied to measure oxylipins in large studies. Abstract Oxylipins are downstream lipid mediators enzymatically-produced from polyunsaturated fatty acids (PUFA) that are implicated as the biological effectors of these fatty acids. Recently reported methods for the quantitation of oxylipins require complex extraction procedures. In this study, we report the development and validation of a novel system for the quantitation of 21 individual oxylipins from a dried blood spot (DBS) using ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) and stable isotope dilution analysis. Linearity and precision of the method were determined and the stabilities of the 12 most abundant oxylipins were tested during 2 months of storage at room temperature, after being spiked into blood and prepared as DBS on PUFAcoat™ paper. Responses were linear across the concentration range analysed for all oxylipins (r2 values ranged from 0.953 to 0.998). Intra-day and inter-day variations were ≤16% for all oxylipins. Recovery of oxylipins from the DBS ranged from 80 - 115%. The 12 spiked oxylipins were stable for 2 months when stored as DBS at room temperature. Our method is reproducible and precise, and provides the opportunity to accurately quantitate these oxylipins in a small sample volume.Copyright © 2018. Published by Elsevier Ltd.

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