Simultaneous preconcentration, identification, and quantitation of selenoamino acids in oils by enantioselective high performance liquid chromatography and mass spectrometry

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Standard

Simultaneous preconcentration, identification, and quantitation of selenoamino acids in oils by enantioselective high performance liquid chromatography and mass spectrometry. / Capriotti, Anna Laura; Montone, Carmela Maria; Antonelli, Michela; Cavaliere, Chiara; Gasparrini, Francesco; La Barbera, Giorgia; Piovesana, Susy; Laganà, Aldo.

I: Analytical Chemistry, Bind 90, Nr. 14, 2018, s. 8326-8330.

Publikation: Bidrag til tidsskriftTidsskriftartikelfagfællebedømt

Harvard

Capriotti, AL, Montone, CM, Antonelli, M, Cavaliere, C, Gasparrini, F, La Barbera, G, Piovesana, S & Laganà, A 2018, 'Simultaneous preconcentration, identification, and quantitation of selenoamino acids in oils by enantioselective high performance liquid chromatography and mass spectrometry', Analytical Chemistry, bind 90, nr. 14, s. 8326-8330. https://doi.org/10.1021/acs.analchem.8b02089

APA

Capriotti, A. L., Montone, C. M., Antonelli, M., Cavaliere, C., Gasparrini, F., La Barbera, G., Piovesana, S., & Laganà, A. (2018). Simultaneous preconcentration, identification, and quantitation of selenoamino acids in oils by enantioselective high performance liquid chromatography and mass spectrometry. Analytical Chemistry, 90(14), 8326-8330. https://doi.org/10.1021/acs.analchem.8b02089

Vancouver

Capriotti AL, Montone CM, Antonelli M, Cavaliere C, Gasparrini F, La Barbera G o.a. Simultaneous preconcentration, identification, and quantitation of selenoamino acids in oils by enantioselective high performance liquid chromatography and mass spectrometry. Analytical Chemistry. 2018;90(14):8326-8330. https://doi.org/10.1021/acs.analchem.8b02089

Author

Capriotti, Anna Laura ; Montone, Carmela Maria ; Antonelli, Michela ; Cavaliere, Chiara ; Gasparrini, Francesco ; La Barbera, Giorgia ; Piovesana, Susy ; Laganà, Aldo. / Simultaneous preconcentration, identification, and quantitation of selenoamino acids in oils by enantioselective high performance liquid chromatography and mass spectrometry. I: Analytical Chemistry. 2018 ; Bind 90, Nr. 14. s. 8326-8330.

Bibtex

@article{ebcade34bec049f3a0ca9601e69c46f2,
title = "Simultaneous preconcentration, identification, and quantitation of selenoamino acids in oils by enantioselective high performance liquid chromatography and mass spectrometry",
abstract = "Selenium is an essential micronutrient for humans. In food, selenium can be present in both inorganic and organic forms, the latter mainly being selenomethionine, Se-methyl-selenocysteine, and selenocystine. Selenoamino acid speciation rarely involves the chirality of selenoamino acids. In this work, a 5 cm long CHIROBIOTIC TAG chromatographic column was used for enantioresolution of selenoamino acids (d- and l-selenomethionine, Se-methyl-l-selenocysteine, d-, l- and meso-selenocystine); in the optimized conditions, the complete resolution of the analytes was achieved within 15 min by using a very polar aqueous mobile phase (gradient elution by methanol/acetonitrile/H2O, 45:45:10 (v/v/v) with 10 mmol L-1 of ammonium formate and 0.5% formic acid as the mobile phase A and acetonitrile/H2O, 20:80 (v/v) with 20 mmol L-1 of ammonium formate at apparent pH 4 as the mobile phase B). The affinity of the teicoplanin aglycone was further exploited to devise a preconcentration method for selenoamino acids in oils. In particular, the CHIROBIOTIC TAG precolumn was used to directly concentrate the selenoamino acids after simple dilution of oil samples with dichloromethane. An optimized procedure for selenoamino acid trapping and preconcentration under normal phase conditions was developed. The enrichment procedure also ensured band focusing during the subsequent separation. The target analytes were finally identified and quantified by triple quadrupole selected reaction monitoring. The method allowed obtainment of recovery values up to 73%, with limits of detection between 280 and 750 ng and limits of quantification between 375 and 960 ng for the different selenoamino acids. The method was applied to commercial oil samples, and only l-selenomethionine was detected.",
author = "Capriotti, {Anna Laura} and Montone, {Carmela Maria} and Michela Antonelli and Chiara Cavaliere and Francesco Gasparrini and {La Barbera}, Giorgia and Susy Piovesana and Aldo Lagan{\`a}",
note = "(Ekstern)",
year = "2018",
doi = "10.1021/acs.analchem.8b02089",
language = "English",
volume = "90",
pages = "8326--8330",
journal = "Industrial And Engineering Chemistry Analytical Edition",
issn = "0003-2700",
publisher = "American Chemical Society",
number = "14",

}

RIS

TY - JOUR

T1 - Simultaneous preconcentration, identification, and quantitation of selenoamino acids in oils by enantioselective high performance liquid chromatography and mass spectrometry

AU - Capriotti, Anna Laura

AU - Montone, Carmela Maria

AU - Antonelli, Michela

AU - Cavaliere, Chiara

AU - Gasparrini, Francesco

AU - La Barbera, Giorgia

AU - Piovesana, Susy

AU - Laganà, Aldo

N1 - (Ekstern)

PY - 2018

Y1 - 2018

N2 - Selenium is an essential micronutrient for humans. In food, selenium can be present in both inorganic and organic forms, the latter mainly being selenomethionine, Se-methyl-selenocysteine, and selenocystine. Selenoamino acid speciation rarely involves the chirality of selenoamino acids. In this work, a 5 cm long CHIROBIOTIC TAG chromatographic column was used for enantioresolution of selenoamino acids (d- and l-selenomethionine, Se-methyl-l-selenocysteine, d-, l- and meso-selenocystine); in the optimized conditions, the complete resolution of the analytes was achieved within 15 min by using a very polar aqueous mobile phase (gradient elution by methanol/acetonitrile/H2O, 45:45:10 (v/v/v) with 10 mmol L-1 of ammonium formate and 0.5% formic acid as the mobile phase A and acetonitrile/H2O, 20:80 (v/v) with 20 mmol L-1 of ammonium formate at apparent pH 4 as the mobile phase B). The affinity of the teicoplanin aglycone was further exploited to devise a preconcentration method for selenoamino acids in oils. In particular, the CHIROBIOTIC TAG precolumn was used to directly concentrate the selenoamino acids after simple dilution of oil samples with dichloromethane. An optimized procedure for selenoamino acid trapping and preconcentration under normal phase conditions was developed. The enrichment procedure also ensured band focusing during the subsequent separation. The target analytes were finally identified and quantified by triple quadrupole selected reaction monitoring. The method allowed obtainment of recovery values up to 73%, with limits of detection between 280 and 750 ng and limits of quantification between 375 and 960 ng for the different selenoamino acids. The method was applied to commercial oil samples, and only l-selenomethionine was detected.

AB - Selenium is an essential micronutrient for humans. In food, selenium can be present in both inorganic and organic forms, the latter mainly being selenomethionine, Se-methyl-selenocysteine, and selenocystine. Selenoamino acid speciation rarely involves the chirality of selenoamino acids. In this work, a 5 cm long CHIROBIOTIC TAG chromatographic column was used for enantioresolution of selenoamino acids (d- and l-selenomethionine, Se-methyl-l-selenocysteine, d-, l- and meso-selenocystine); in the optimized conditions, the complete resolution of the analytes was achieved within 15 min by using a very polar aqueous mobile phase (gradient elution by methanol/acetonitrile/H2O, 45:45:10 (v/v/v) with 10 mmol L-1 of ammonium formate and 0.5% formic acid as the mobile phase A and acetonitrile/H2O, 20:80 (v/v) with 20 mmol L-1 of ammonium formate at apparent pH 4 as the mobile phase B). The affinity of the teicoplanin aglycone was further exploited to devise a preconcentration method for selenoamino acids in oils. In particular, the CHIROBIOTIC TAG precolumn was used to directly concentrate the selenoamino acids after simple dilution of oil samples with dichloromethane. An optimized procedure for selenoamino acid trapping and preconcentration under normal phase conditions was developed. The enrichment procedure also ensured band focusing during the subsequent separation. The target analytes were finally identified and quantified by triple quadrupole selected reaction monitoring. The method allowed obtainment of recovery values up to 73%, with limits of detection between 280 and 750 ng and limits of quantification between 375 and 960 ng for the different selenoamino acids. The method was applied to commercial oil samples, and only l-selenomethionine was detected.

UR - http://www.scopus.com/inward/record.url?scp=85048770401&partnerID=8YFLogxK

U2 - 10.1021/acs.analchem.8b02089

DO - 10.1021/acs.analchem.8b02089

M3 - Journal article

C2 - 29909624

AN - SCOPUS:85048770401

VL - 90

SP - 8326

EP - 8330

JO - Industrial And Engineering Chemistry Analytical Edition

JF - Industrial And Engineering Chemistry Analytical Edition

SN - 0003-2700

IS - 14

ER -

ID: 231312681