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1. Methods of Metabolite Identification Using MS/MS Data

   https://doi.org/10.1080/08874417.2019.1681328  

   Kwak, Myungjae; Kang, Kyungwoo; Wang, Yingfeng (January 2022, Journal of Computer Information Systems)
2. Analysis of oil-based ignitable liquid residues by GC–MS and DART–MS

   https://doi.org/10.1016/j.forc.2025.100701  

   Dong, Wen; Chong, Ngee Sing; Thanni, Qudus Ayodeji; de_Boves_Harrington, Peter; Zhang, Mengliang (September 2025, Forensic Chemistry)

   Fatty acid-based ignitable liquids (ILs), such as biodiesels and bio-based lighter fluids, represent a growing class of accelerants with limited forensic characterization. In this study, we applied gas chromatography–mass spectrometry (GC–MS) and direct analysis in real time mass spectrometry (DART–MS) to analyze plant oil-derived IL residues on wood and fabric substrates. ILs were prepared from ten different plant oils, subjected to burning, and extracted from fire debris using the ASTM E1412 activated charcoal method. GC–MS analysis resolved characteristic fatty acid methyl esters (FAMEs) and identified diagnostic fragment ions (m/z 55, 67, 74, 79). The fragmentation patterns of unsaturated and saturated FAMEs were systematically examined and compared against experimental data and reference spectra from online databases, demonstrating strong agreement and validating the reliability of these ion ratios as qualitative indicators of FAME saturation. DART–MS enabled rapid confirmation of major unsaturated FAMEs through the detection of protonated molecular ions, offering complementary identification without chromatographic separation. Chemometric analysis using principal component analysis (PCA) and analysis of variance-PCA revealed that FAME profiles were strongly dependent on the IL sources and remained reliable across replicate preparations and synthesis conditions, while substrate and combustion effects were mitigated using targeted ion extraction. These findings demonstrate the practical casework relevance of combining GC–MS and DART–MS for the detection and classification of fatty acid–based ILs in fire debris, providing robust chemical evidence to support arson investigations and to guide the inclusion of these emerging accelerants in forensic ignitable-liquid classification schemes. 

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3. Separation, identification, and confirmation of cyclic and tadpole macromolecules via UPLC-MS/MS

   https://doi.org/10.1039/d2an00208f  

   O'Neill, Jason M.; Mao, Jialin; Haque, Farihah M.; Barroso-Bujans, Fabienne; Grayson, Scott M.; Wesdemiotis, Chrys (May 2022, The Analyst)

   Macrocyclic poly(glycidyl phenyl ether) (pGPE) synthesized via zwitterionic ring opening polymerization is typically contaminated by chains with linear and tadpole architecture. Although mass spectrometry (MS) analysis can readily confirm the presence of the linear byproduct, due to its unique mass, it is unable to differentiate between the cyclic and tadpole structures, which are constitutional isomers produced by backbiting reactions in monomeric or dimeric chains, respectively. To overcome this problem, ultraperformance reversed-phase liquid chromatography interfaced with electrospray ionization tandem mass spectrometry (UPLC-ESI-MS/MS) was employed. The separation achieved by UPLC revealed that the tadpole isomer elutes before the cyclic structure because of the increased polarity afforded by its distinctive substituents. The ratio of tadpole to cyclic species increased with the degree of polymerization, in agreement with the synthetic method used, as the potential for forming tadpole structures by backbiting is entropically favored in longer polymer chains. Once separated, the two isomers could be independently characterized by tandem mass spectrometry. The macrocyclic and tadpole species exhibit unique fragmentation patterns, including structurally diagnostic fragments for each structure. 

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4. U-Pb dating of accessory minerals by LA-ICP-MS/MS

   Stone, JS; Cruz-Uribe, AM; Brooks, HL; Walters, J (January 2019, 2019 Fall Meeting AGU)

   Titanite and apatite can incorporate significant amounts of common Pb (204Pb) into their mineral structures, which leads to uncertainty when applying the U-Pb decay series for geochronology. The isobaric interference between 204Pb and 204Hg creates an additional complexity when calculating common lead corrections. Here we investigate the removal of 204Hg interferences during titanite U-Pb dating using reaction cell gas chemistry via triple quadrupole mass spectrometry compared with traditional methods that calculate U-Pb ages using a common lead correction. U-Pb dates for titanite natural reference materials MKED-1 and BLR-1 were determined using an ESI NWR193UC excimer laser coupled with an Agilent 8900 ‘triple quadrupole’ mass spectrometer. The 8900 is equipped with an octopole collision/reaction cell, which enables online interference removal. In order to compare traditional methods for U-Pb dating with interference removal methods, two experiments were run, one in which data was collected in NoGas mode, and one in which the 8900 was run in MS/MS mode, in order to assess the feasibility of determining U/Pb ratios with mass shifted isotopes. In MS/MS mode, NH3 was flowed through the reaction cell in order to enable a charge transfer reaction between NH3 and Hg+, effectively neutralizing Hg. During spot analyses in NoGas mode, masses 202Hg, 204Hg, 204Pb, 206Pb, 207Pb, 208Pb, 232Th, 235U, and 238U were monitored. For spot analyses in MS/MS mode, Th and U isotopes were measured on-mass at 232Th, 235U, 238U and mass-shifted to 247Th, 250U, and 253U. Pb isotopes were measured on-mass since Pb does not react with NH3. Ratios for 207Pb/235U, 206Pb/238U, and 207Pb/206Pb were calculated in Iolite (v.3.7.1) using the Geochron4 DRS using MKED-1 as the primary reference material and BLR-1 as a secondary reference material. Dates were calculated using IsoplotR. Weighted mean ages for titanite BLR-1 in MS/MS mode are 1043.8 ± 10.5 Ma (2σ, MSWD=1.08) for U isotopes measured on mass, and 1039.7 ± 8.3 Ma (2σ, MSWD=1.08) for mass-shifted U isotopes. These dates are both in agreement with the TIMS 206Pb/238U date for the BLR-1 titanite of 1047.1 ± 0.4 Ma. The use of NH3 for reaction cell chemistry has the potential to enable measurement of 204Pb without needing to correct for Hg interferences. 

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5. LC/MS at the whole protein level: Studies of biomolecular structure and interactions using native LC/MS and cross-path reactive chromatography (XP-RC) MS

   https://doi.org/10.1016/j.ymeth.2018.04.019  

   Kaltashov, Igor A.; Pawlowski, Jake W.; Yang, Wenhua; Muneeruddin, Khaja; Yao, Honglin; Bobst, Cedric E.; Lipatnikov, Andrei N. (July 2018, Methods)