Comparing the quantitation of specialized pro-resolving mediators in plasma and serum using ELISA and LC-MS/MS

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Authors: Brendon Naicker, Vindya Ramanayake-Mudiyanselage, Tanya Maxey, Victoria J. Tyrrell, J. Horn, Paul D. Kennedy, Daniel J. Tew, Jeff Johnson, Garret A FitzGerald, Robert C Murphy, Kirk M. Maxey, Valerie B O’Donnell
+1 more Miguel A. Gijón
Cited by: 4
References: 35

Abstract

Quantitation of oxylipins is generally performed using liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS). Researchers can also use commercial enzyme-linked immunosorbent assays (ELISAs), due to convenience or where access to instrumentation is limited. However, oxylipins are small molecules with many isomers and metabolites that are difficult to fully discriminate using ELISAs, with many potential sources of cross-reactivity. In this paper, the use of ELISAs for oxylipin analysis is compared with LC-MS/MS, with two specialized pro-resolving mediators (SPM) as examples. By reviewing the literature, we show that ELISAs report significantly higher levels of resolvin D1 (RvD1) and resolvin D2 (RvD2) than LC-MS/MS. Also, we show experimentally that in plasma and serum samples where these lipids were not detected using LC-MS/MS, a positive result could be obtained using ELISA, and that these signals increase with improper sample processing. In conclusion, while ELISA could be a useful technique for detecting the presence of oxylipins, positive signals need verification using LC-MS/MS.

Fields of Study & Subjects

S100 Proteins and Annexins Eicosanoids and Hypertension Pharmacology Protein Kinase Regulation and GTPase Signaling

Publication details

Journal / source
Prostaglandins Leukotrienes and Essential Fatty Acids
Publisher
Elsevier BV
Volume
209
Pages
102731–102731
Publication date
7 March 2026
Language
EN