4.6 Article

Tailored Polymer-Based Selective Extraction of Lipid Mediators from Biological Samples

期刊

METABOLITES
卷 11, 期 8, 页码 -

出版社

MDPI
DOI: 10.3390/metabo11080539

关键词

lipid mediators; molecularly imprinted polymer (MIP); non-imprinted polymer (NIP); strata-X; solid-phase extraction (SPE)

资金

  1. National Research Foundation, Singapore [NRFSBP-P4]
  2. Agency for Science, Technology and Research, Singapore [IAF-ICP I1901E0040]
  3. National University of Singapore via the Life Sciences Institute (LSI)

向作者/读者索取更多资源

The study presents a rapid and selective extraction method using new low-cost molecularly imprinted and non-imprinted polymeric sorbents for lipid mediators from plasma and tissue samples. The method was validated by quantifying lipid mediators through liquid chromatography-tandem mass spectrometry, demonstrating advantages in extraction efficiency and reduction of non-specific interactions.
Lipid mediators, small molecules involved in regulating inflammation and its resolution, are a class of lipids of wide interest as their levels in blood and tissues may be used to monitor health and disease states or the effect of new treatments. These molecules are present at low levels in biological samples, and an enrichment step is often needed for their detection. We describe a rapid and selective method that uses new low-cost molecularly imprinted (MIP) and non-imprinted (NIP) polymeric sorbents for the extraction of lipid mediators from plasma and tissue samples. The extraction process was carried out in solid-phase extraction (SPE) cartridges, manually packed with the sorbents. After extraction, lipid mediators were quantified by liquid chromatography-tandem mass spectrometry (LC-MSMS). Various parameters affecting the extraction efficiency were evaluated to achieve optimal recovery and to reduce non-specific interactions. Preliminary tests showed that MIPs, designed using the prostaglandin biosynthetic precursor arachidonic acid, could effectively enrich prostaglandins and structurally related molecules. However, for other lipid mediators, MIP and NIP displayed comparable recoveries. Under optimized conditions, the recoveries of synthetic standards ranged from 62% to 100%. This new extraction method was applied to the determination of the lipid mediators concentration in human plasma and mouse tissues and compared to other methods based on commercially available cartridges. In general, the methods showed comparable performances. In terms of structural specificity, our newly synthesized materials accomplished better retention of prostaglandins (PGs), hydroxydocosahexaenoic acid (HDoHE), HEPE, hydroxyeicosatetraenoic acids (HETE), hydroxyeicosatrienoic acid (HETrE), and polyunsaturated fatty acid (PUFA) compounds, while the commercially available Strata-X showed a higher recovery for dihydroxyeicosatetraenoic acid (diHETrEs). In summary, our results suggest that this new material can be successfully implemented for the extraction of lipid mediators from biological samples.

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