2017
DOI: 10.1007/978-1-4939-6946-3_12
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HPTLC-MALDI TOF MS Imaging Analysis of Phospholipids

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Cited by 1 publication
(4 citation statements)
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“…The magnitude of the emission can be modulated by the choice of the fluorophore, its concentration and the chromatographic parameters. [11] Lipids do not form adducts with primuline [60] which is compatible with MS for characterization, either in MAL-DI, [61,62] DESI, [56,57] or ESI and APCI through an elution-based HPTLC-MS interface. [12] Reversibility of staining was also mentioned.…”
Section: Organic Revealing Agentsmentioning
confidence: 88%
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“…The magnitude of the emission can be modulated by the choice of the fluorophore, its concentration and the chromatographic parameters. [11] Lipids do not form adducts with primuline [60] which is compatible with MS for characterization, either in MAL-DI, [61,62] DESI, [56,57] or ESI and APCI through an elution-based HPTLC-MS interface. [12] Reversibility of staining was also mentioned.…”
Section: Organic Revealing Agentsmentioning
confidence: 88%
“…A TLC-plate adapter and software were introduced in 2007 by Bruker Daltonics [61] for directly accomplishing qualitative structural characterization and screening of lipids on the plate. [21,23,51,58,59,62,65,71,75,78,84,117,[126][127][128][129][130][131][132] In a similar way that MS imaging allows the recording of spatially resolved mass spectra from slices of biological tissues, MALDI has also been used to monitor the distribution of selected lipids on the HPTLC plate. For this, peak intensities, in dependence of the position, were converted into gray or a color scale.…”
Section: Ionizaon and Matricesmentioning
confidence: 99%
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