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Opioid addiction is an escalating problem that is compounded by the introduction of synthetic opiate analogues such as fentanyl. Screening methods for these compound classes are challenged by the availability of synthetically manufactured analogues, including isomers of existing substances. High-field asymmetric-waveform ion mobility spectrometry (FAIMS) utilizes an alternating asymmetric electric field to separate ions by their different mobilities at high and low fields as they travel through the separation space. When coupled to mass spectrometry (MS), FAIMS enhances the separation of analytes from other interfering compounds with little to no increase in analysis time. Addition of solvent vapor into the FAIMS carrier gas has been demonstrated to enable and improve the separation of isomers. Here we investigate the effects of several solvents for the separation of four opioids. FAIMS-MS spectra with added solvent vapors show dramatic compensation field (CF) shifts for opioid [M+H]+ ions when compared to spectra acquired using dry nitrogen. Addition of vapor from aprotic solvents, such as acetonitrile and acetone, produces significantly improved resolution between the tested opioids, with baseline resolution achieved between certain opioid isomers. For protic solvents, notable CF shift differences were observed in FAIMS separations between addition of water vapor and vapors from small alcohols. [ABSTRACT FROM AUTHOR]

In recent years, metabolomics and lipidomics approaches have become increasingly popular for use in the analysis of human heath, molecular mechanisms, and disease progression. Despite the growth in applications and advances in instrumentation, metabolomics and lipidomics are limited by factors including interference from matrix effects, the need for lengthy for chromatographic analysis, and structural diversity of metabolites and lipids creating interference of isomers and isobars, which can confound identification. Ion mobility spectrometry (IMS) provides a method to enhance throughput, enhance isomeric separation, and reduce chemical noise. This review focuses on (i) the use of IMS and subsequent advancements in global metabolomics and lipidomics, (ii) the application and benefits of IMS in targeted metabolomics studies, and (iii) the use of IMS for non-chromatographic methods such as direct analysis, desorption ionization methods, and imaging. • Integration of ion mobility spectrometry (IMS) enhances isomeric separation. • IMS improves metabolome coverage. • IMS mass spectrometry imaging enhances spatial characterization of tissues. • Addition of collision cross sections to metabolite databases are needed. [ABSTRACT FROM AUTHOR]