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Fatty acids (FAs) are essential molecules in biological systems and have crucial roles for fundamental components of cellular membranes, energy stores and mediators for cellular functions. The growing importance of FAs has also paid attention to analytical methods for the determination of FA contents in various samples accurately. Liquid chromatography tandem mass spectrometry (LC-MS/MS) analysis is a powerful tool due to less time for sample preparation and analysis. This analytical approach enables to quantify levels of FA and other lipid classes in various samples simultaneously without derivatization. In the present study, the effects of ammonium salts on the sensitivity of FAs in LC-MS/MS analysis were evaluated. First, authors performed the comparison of FA analysis with different mobile phases, which contain ammonium formate, ammonium fluoride, ammonium acetate or ammonium carbonate. Interestingly, the mobile phase containing ammonium fluoride enhanced the sensitivity of targeted FA species more than other ammonium salts. Second, the difference of quantativity of FA species was examined. It was indicated that both carbon chain length and the number of double bonds affect ionization of FA species. Finally, the method of FA analysis based on ammonium fluoride was applied to FA profiling of lotus root. It is indicated that mobile phase containing ammonium fluoride enabled to evaluate FA contents with highly sensitivity in LC-MS/MS analysis.
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http://dx.doi.org/10.1007/s44211-025-00832-7 | DOI Listing |
Antipyretic analgesics are typical pharmaceutical and personal care products (PPCPs) that are widely used in our daily life because they relieve fever and pain, and have anti-inflammatory and anti-rheumatic properties. These drugs inhibit the synthesis and release of prostaglandins (PGs) in the neurons of the anterior hypothalamus and exert therapeutic effects as a consequence. However, these drugs are relatively commonly misused and abused, often owing to a lack of proper medication guidance.
View Article and Find Full Text PDFBisphenol A (BPA) and its analogs are collectively termed bisphenol compounds (BPs), which are predominantly utilized in the manufacturing of polycarbonate plastics and epoxy resins. BPs are ubiquitous in diverse environmental matrices, human tissues, and metabolic products. Extensive research has demonstrated that BPs exert adverse effects on the nervous, reproductive, immune, and metabolic systems.
View Article and Find Full Text PDFAnal Sci
August 2025
Faculty of Pharmacy, Yasuda Women's University, Yasuhigashi 6-13-1, Asaminami-Ku, Hiroshima, 731-0153, Japan.
Fatty acids (FAs) are essential molecules in biological systems and have crucial roles for fundamental components of cellular membranes, energy stores and mediators for cellular functions. The growing importance of FAs has also paid attention to analytical methods for the determination of FA contents in various samples accurately. Liquid chromatography tandem mass spectrometry (LC-MS/MS) analysis is a powerful tool due to less time for sample preparation and analysis.
View Article and Find Full Text PDFJ Chromatogr A
October 2025
Laboratory of Pharmaceutical Analytical Chemistry, Gifu Pharmaceutical University, Daigaku-nishi, Gifu, 501-1196, Japan; United Graduate School of Drug Discovery and Medical Information Sciences, Gifu University, 1-1 Yanagido, Gifu 501-1194, Japan. Electronic address:
Short-chain fatty acids (SCFAs), such as acetic, propionic, and butyric acid, are important biomarkers that reflect gut microbiota composition, disease progression, and overall health. Conventional SCFA analysis typically involves derivatization prior to liquid or gas chromatography. However, derivatization is challenging due to the volatility of SCFAs and interference from similar carboxylic acids in biological samples and often requires complex purification steps.
View Article and Find Full Text PDFJ Am Soc Mass Spectrom
August 2025
Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-0146, United States.
In the course of synthetic work and mass spectrometry (MS) with hydroxy steroids, we observed not only the loss of HO but prominent 2 and 4 amu losses using atmospheric pressure chemical ionization (APCI), leading to confusion of the structural assignments. This loss of 2 amu, which we attributed mainly to oxidation of hydroxyls, varied among 44 steroids and sterols analyzed; 36 showed losses of 2 amu in APCI MS analysis (17/22 Δ steroids, 17/19 Δ steroids, and 2/3 estrogens). With the Δ steroids and sterols, the precursor MH was either observed as a minor ion or (more frequently) not detected at all, constituting the base peak in 7/22 cases.
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