This study describes the use of hybrid mass spectrometry for the mapping, identification, and semi-quantitation of triacylglycerol regioisomers in fats and oils. The identification was performed based on the accurate mass and fragmentation pattern obtained by data-dependent fragmentation. Quantitation was based on the high-resolution ion chromatograms, and relative proportion of sn-1(3)/sn-2 regioisomers was calculated based on generalized fragmentation models and the relative intensities observed in the product ion spectra. The key performance features of the developed method are inter-batch mass accuracy < 1 ppm (n = 10); lower limit of detection (triggering threshold) 0.1 μg/ml (equivalent to 0.2 weight % in oil); lower limit of quantitation 0.2 μg/ml (equivalent to 0.4 weight % in oil); peak area precision 6.5% at 2 μg/ml concentration and 15% at 0.2 μM concentration; inter-batch precision of fragment intensities < 1% (n = 10) independent of the investigated concentration; and averaged accuracy using the generic calibration 3.8% in the 1-10 μg/ml range and varies between 1-23% depending on analytes. Inter-esterified fat, beef tallow, pork lard, and butter fat samples were used to show how well regioisomeric distribution of palmitic acid can be captured by this method.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520536 | PMC |
http://dx.doi.org/10.1194/jlr.D031484 | DOI Listing |
J Nat Prod
April 2024
School of Pharmacy, Fudan University, Shanghai 201203, China.
The plant of the Annonaceae family is used as an alternative medicine in tropical regions. Applying high-speed counter current chromatography (HSCCC), eight new bioactive styrylpyrone isomers, including 6,7,8,2'-goniolactone B (), 6,7,8,2'-goniolactone B (), 6,7,8,2'-goniolactone B (), 6,7,8,2'-goniolactone C (), 6,7,8,2'-goniolactone C (), 6,7,8,2'-goniolactone C (), and two positional isomers, 6,7,8,2'-goniolactone G () and 6,7,8,2'-goniolactone G (), were isolated from a chloroform fraction (2.1 g) of , which had a prominent spot by TLC analysis.
View Article and Find Full Text PDFAnal Chem
December 2023
Department of Chemistry - BMC, Uppsala University, 75123 Uppsala, Sweden.
Identifying and mapping steroids in tissues can provide opportunities for biomarker discovery, the interrogation of disease progression, and new therapeutics. Although separation coupled to mass spectrometry (MS) has emerged as a powerful tool for studying steroids, imaging and annotating steroid isomers remains challenging. Herein, we present a new method based on the fragmentation of silver-cationized steroids in tandem MS, which produces distinctive and consistent fragmentation patterns conferring confidence in steroid annotation at the regioisomeric level without using prior derivatization, separation, or instrumental modification.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
April 2023
Beijing National Laboratory for Molecular Sciences, Key Laboratory of Molecular Nanostructure and Nanotechnology, Institute of Chemistry, Chinese Academy of Sciences, Zhongguancun North First Street No.2, Beijing, 100190, China.
Understanding the influence of molecular structure on charge distribution and charge separation (CS) provides essential guidance for optoelectronic materials design. Here we propose a regioisomeric strategy to tune the diverse hole-distribution, and probe the influence on CS patterns. Para-, meta- and ortho-substituted benzidine-fullerene, named 1 p, 1 m and 1 o are designed.
View Article and Find Full Text PDFInt J Mol Sci
January 2023
Department of Chemistry and Chemical Technologies (CTC), University of Calabria-UNICAL, Via P. Bucci, Arcavacata di Rende, 87036 Rende, Italy.
Org Biomol Chem
February 2023
University of Belgrade - Faculty of Chemistry, Studentski trg 12-16, P.O.Box 158, 11000 Belgrade, Serbia.
We present the green, highly atom-economical, solid-state silica gel-catalyzed synthesis of polysubstituted 1,4- and 1,2-dihydropyridines (DHPs) from commercially available materials, amines and ethyl propiolate. The DHP skeleton was assembled by heating the reactants and silica gel in a closed vessel. Aliphatic amines provided 1,4-isomers as the main or only DHP products, but the reactions of aromatic amines yielded a mixture of 1,4- and 1,2-isomers.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!