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Building an empirical mass spectra library for screening of organic pollutants by ultra‐high‐pressure liquid chromatography/hybrid quadrupole time‐of‐flight mass spectrometry
Author(s) -
Díaz Ramón,
Ibáñez María,
Sancho Juan V.,
Hernández Félix
Publication year - 2010
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/rcm.4860
Subject(s) - chemistry , mass spectrometry , analyser , mass spectrum , analytical chemistry (journal) , time of flight mass spectrometry , calibration , mass , chromatography , ion , ionization , organic chemistry , statistics , mathematics
Hybrid quadrupole time‐of‐flight mass spectrometry (QTOF MS) has gained wide acceptance in many fields of chemistry, for example, proteomics, metabolomics and small molecule analysis. This has been due to the numerous technological advances made to this mass analyser in recent years. In the environmental field, the instrument has proven to be one of the most powerful approaches for the screening of organic pollutants in different matrices due to its high sensitivity in full acquisition mode and mass accuracy measurements. In the work presented here, the optimum experimental conditions for the creation of an empirical TOF MS spectra library have been evaluated. For this model we have used a QTOF Premier mass spectrometer and investigated its functionalities to obtain the best MS data, mainly in terms of mass accuracy, dynamic range and sensitivity. Different parameters that can affect mass accuracy, such as lock mass, ion abundance, spectral resolution, instrument calibration or matrix effect, have also been carefully evaluated using test compounds (mainly pesticides and antibiotics). The role of ultra‐high‐pressure liquid chromatography (UHPLC), especially when dealing with complex matrices, has also been tested. In addition to the mass accuracy measurements, this analyser allows the simultaneous acquisition of low and high collision energy spectra. This acquisition mode greatly enhances the reliable identification of detected compounds due to the useful (de)protonated molecule and fragment ion accurate mass information obtained when working in this mode. An in‐house empirical spectral library was built for approximately 230 organic pollutants making use of QTOF MS in MS E mode. All the information reported in this paper is made available to the readers to facilitate screening and identification of relevant organic pollutants by QTOF MS. Copyright © 2010 John Wiley & Sons, Ltd.

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