2017
DOI: 10.1177/1469066717711026
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Dependence of matrix effect on ionization polarity during LC–ESI–MS analysis of derivatized amino acids in some natural samples

Abstract: Matrix effect, the influence of co-eluting components on the ionization efficiency of the analyte, affects the trueness and precision of the LC-ESI-MS analysis. Derivatization can reduce or eliminate matrix effect, for example, diethyl ethoxymethylenemalonate (DEEMM) derivatives have shown less matrix effect compared to other derivatives. Moreover, the use of negative ion mode can further reduce matrix effect. In order to investigate the combination of derivatization and different ionization modes, an LC-ESI-M… Show more

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Cited by 12 publications
(9 citation statements)
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“…(Elmsjo et al, 2017;Gika, Theodoridis, Plumb, & Wilson, 2014). However, MS has a matrix effect and can only detect ionized substances (Oldekop, Rebane, & Herodes, 2017). Metabolites that are not ionizable can be detected by NMR.…”
Section: Introductionmentioning
confidence: 99%
“…(Elmsjo et al, 2017;Gika, Theodoridis, Plumb, & Wilson, 2014). However, MS has a matrix effect and can only detect ionized substances (Oldekop, Rebane, & Herodes, 2017). Metabolites that are not ionizable can be detected by NMR.…”
Section: Introductionmentioning
confidence: 99%
“…This is in accordance to other studies, in which was shown that ion suppression is less occurring in negative ionization mode. 24,25 Although the FIA method is faster (1.4 versus 3 min), the findings in Figure 3 emphasize the necessity of online fractionation prior to electrospray ionization.…”
mentioning
confidence: 98%
“…A UHPLC-MS method was developed for the detection of derivatized amino compounds in neutral loss scan mode, by exploiting the characteristic DEEMM fragmentation pattern. All analyses were performed in positive ionization mode, due to the lower MS intensity of DEEMM derivatives (especially biogenic amines) in negative ESI mode, and because the investigated neutral fragment originates from the positively charged compounds [6,12,31].…”
Section: Optimization Of the Derivatization Proceduresmentioning
confidence: 99%