Assessing the capabilities of direct analysis in real time mass spectrometry for 5-hydroxymethylfurfural quantitation in honey

The limitations of direct analysis in real time mass spectrometry (DART-MS) were shown with the example of 5-hydroxymethylfurfural (HMF) quantitation in honey. An accurate analyte quantitation was impossible because the carbohydrate matrix partially degraded to the analyte in the ionization region. However, at a decreased DART temperature of 150 °C, the DART-MS screening was possible using two spiked reference samples. The influence of instrumental parameters on the composition of the DART mass spectra for HMF and carbohydrates was investigated. Also, first data on scanning surface analysis with DART-MS were obtained giving rise for further studies in this direction. © 2012 Elsevier B.V. All rights reserved

Coupling of planar chromatography with Direct Analysis in Real Time mass spectrometry

Direct Analysis in Real Time mass spectrometry (DART-MS) is an emerging and rapidly developing area of ambient desorption ionization mass spectrometric techniques. Its coupling with planar chromatography is especially promising, as compared to other ambient desorption ionization techniques, because it does not require the use of liquids that may distort the shape of a spot by diffusion effects. In the first publications on TLC/HPTLC-DART-MS, due to the fixed, horizontally aligned supply of the gas flow from the DART ionization source to the MS inlet, the introduction of HPTLC/TLC plates as cut strips was inconvenient for quantitation, and the repeatability was very low due to the manual positioning. Recently a new version of the DART ion source was suggested, which allows adjusting the angle of the DART gas stream and the use of a motorized rail, thereby, improving highly the capabilities of TLC/HPTLC-DART-MS. This comprehensive review describes the development and analytical capabilities of TLC/HPTLC-DART-MS, and the general DART-MS perspectives for surface analysis or imaging MS. © Versita Sp. z o.o

Ambient desorption ionization mass spectrometry (DART, DESI) and its bioanalytical applications

In recent years, ambient desorption ionization techniques for mass spectrometry were introduced. Among them, the most established techniques are Direct Analysis in Real Time (DART) and Desorption Electrospray Ionization (DESI). Therefore, the current review focuses on the bioanalytical applications of ambient desorption ionization techniques by the example of DART and DESI mass spectrometry. The potential and also limitations of both ambient mass spectrometry (MS) techniques in such areas, as identification and quantitation of small molecules, coupling DART-MS and DESI-MS with planar chromatography, protein/peptide analysis, as well as molecular imaging applications, are discussed. © 2011 Springer-Verlag

High-performance liquid chromatography coupled to mass spectrometry for studying new pharmaceutical entities

The review covers the aspects of the use of high-performance liquid chromatography coupled to mass spectrometry for studying new pharmaceutical entities. Attention is paid mainly to pharmacokinetic investigations. Different methods of sample preparation and approaches to minimize the duration of the analysis are discussed. © 2010, Pleiades Publishing, Ltd

Determination of drugs and drug-like compounds in different samples with direct analysis in real time mass spectrometry

Direct analysis in real time (DART), a relatively new ionization source for mass spectrometry, ionizes small-molecule components from different kinds of samples without any sample preparation and chromatographic separation. The current paper reviews the published data available on the determination of drugs and drug-like compounds in different matrices with DART-MS, including identification and quantitation issues. Parameters that affect ionization efficiency and mass spectra composition are also discussed. © 2011 Wiley Periodicals, Inc

Assessing the capabilities of direct analysis in real time mass spectrometry for 5-hydroxymethylfurfural quantitation in honey

The limitations of direct analysis in real time mass spectrometry (DART-MS) were shown with the example of 5-hydroxymethylfurfural (HMF) quantitation in honey. An accurate analyte quantitation was impossible because the carbohydrate matrix partially degraded to the analyte in the ionization region. However, at a decreased DART temperature of 150 °C, the DART-MS screening was possible using two spiked reference samples. The influence of instrumental parameters on the composition of the DART mass spectra for HMF and carbohydrates was investigated. Also, first data on scanning surface analysis with DART-MS were obtained giving rise for further studies in this direction. © 2012 Elsevier B.V. All rights reserved

Coupling of planar chromatography with Direct Analysis in Real Time mass spectrometry

Direct Analysis in Real Time mass spectrometry (DART-MS) is an emerging and rapidly developing area of ambient desorption ionization mass spectrometric techniques. Its coupling with planar chromatography is especially promising, as compared to other ambient desorption ionization techniques, because it does not require the use of liquids that may distort the shape of a spot by diffusion effects. In the first publications on TLC/HPTLC-DART-MS, due to the fixed, horizontally aligned supply of the gas flow from the DART ionization source to the MS inlet, the introduction of HPTLC/TLC plates as cut strips was inconvenient for quantitation, and the repeatability was very low due to the manual positioning. Recently a new version of the DART ion source was suggested, which allows adjusting the angle of the DART gas stream and the use of a motorized rail, thereby, improving highly the capabilities of TLC/HPTLC-DART-MS. This comprehensive review describes the development and analytical capabilities of TLC/HPTLC-DART-MS, and the general DART-MS perspectives for surface analysis or imaging MS. © Versita Sp. z o.o

Determination of drugs and drug-like compounds in different samples with direct analysis in real time mass spectrometry

Direct analysis in real time (DART), a relatively new ionization source for mass spectrometry, ionizes small-molecule components from different kinds of samples without any sample preparation and chromatographic separation. The current paper reviews the published data available on the determination of drugs and drug-like compounds in different matrices with DART-MS, including identification and quantitation issues. Parameters that affect ionization efficiency and mass spectra composition are also discussed. © 2011 Wiley Periodicals, Inc

High-performance liquid chromatography coupled to mass spectrometry for studying new pharmaceutical entities

The review covers the aspects of the use of high-performance liquid chromatography coupled to mass spectrometry for studying new pharmaceutical entities. Attention is paid mainly to pharmacokinetic investigations. Different methods of sample preparation and approaches to minimize the duration of the analysis are discussed. © 2010, Pleiades Publishing, Ltd