IDENTIFICATION AND DIFFERENTIATION OF UNDERIVATIZED DIASTEROMERIC

Sugars are important molecules with remarkable cell signals pathway functions in higher organisms. The structural complexity of sugar represented by its isomeric, anomeric and diasteromeric configurations deserve the implementation of modern, rapid and sensitive methodologies for its identification...

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Autores principales: Guillermo L. MONTOYA P., Alejandra RENDÓN M., Gabriel J. ARANGO A.
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Publicado: Universidad de Antioquia 2010
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Acceso en línea:https://doaj.org/article/12219e5589e2425d943a60f5d7f84444
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spelling oai:doaj.org-article:12219e5589e2425d943a60f5d7f844442021-11-19T04:14:36ZIDENTIFICATION AND DIFFERENTIATION OF UNDERIVATIZED DIASTEROMERIC0121-40042145-2660https://doaj.org/article/12219e5589e2425d943a60f5d7f844442010-03-01T00:00:00Zhttps://revistas.udea.edu.co/index.php/vitae/article/view/4982https://doaj.org/toc/0121-4004https://doaj.org/toc/2145-2660Sugars are important molecules with remarkable cell signals pathway functions in higher organisms. The structural complexity of sugar represented by its isomeric, anomeric and diasteromeric configurations deserve the implementation of modern, rapid and sensitive methodologies for its identification and differentiation. Mass spectrometry and its analyzer of ion trap provide new alternative techniques that encourage the control of the fragmentation energies supplied to molecules. Since stereoisomer differentiation is consider outside the mass spectrometry domain, a methodology has been applied in order to differentiate β-D-galactose, β-D-glucose and the disaccharides β-D-galactopyranosyl-(1→4)-β-D-glucopyranoside (lactose), α-D-glucopyranosyl-(1→4)-β-D-glucopyranoside (maltose) y β-D-fructofuranosyl-(2↔1)-α- D-glucopyranoside (sacarose) trough its ammonium and lithium adducts by infusion on ESI-IT-MS/MS mass spectrometer. Different fragmentation energies have been used to ensure the ion marker occurrence in the analyte stereochemistry. It is evident that the collision energies control in structural analysis of molecules provides a powerful and modern analytical tool to be applied in control laboratories.Guillermo L. MONTOYA P.Alejandra RENDÓN M.Gabriel J. ARANGO A.Universidad de Antioquiaarticleelectrosprayion trap analyzermonosaccharidesdisaccharidesdiasteromerstandem massFood processing and manufactureTP368-456Pharmaceutical industryHD9665-9675ENVitae, Vol 17, Iss 1 (2010)
institution DOAJ
collection DOAJ
language EN
topic electrospray
ion trap analyzer
monosaccharides
disaccharides
diasteromers
tandem mass
Food processing and manufacture
TP368-456
Pharmaceutical industry
HD9665-9675
spellingShingle electrospray
ion trap analyzer
monosaccharides
disaccharides
diasteromers
tandem mass
Food processing and manufacture
TP368-456
Pharmaceutical industry
HD9665-9675
Guillermo L. MONTOYA P.
Alejandra RENDÓN M.
Gabriel J. ARANGO A.
IDENTIFICATION AND DIFFERENTIATION OF UNDERIVATIZED DIASTEROMERIC
description Sugars are important molecules with remarkable cell signals pathway functions in higher organisms. The structural complexity of sugar represented by its isomeric, anomeric and diasteromeric configurations deserve the implementation of modern, rapid and sensitive methodologies for its identification and differentiation. Mass spectrometry and its analyzer of ion trap provide new alternative techniques that encourage the control of the fragmentation energies supplied to molecules. Since stereoisomer differentiation is consider outside the mass spectrometry domain, a methodology has been applied in order to differentiate β-D-galactose, β-D-glucose and the disaccharides β-D-galactopyranosyl-(1→4)-β-D-glucopyranoside (lactose), α-D-glucopyranosyl-(1→4)-β-D-glucopyranoside (maltose) y β-D-fructofuranosyl-(2↔1)-α- D-glucopyranoside (sacarose) trough its ammonium and lithium adducts by infusion on ESI-IT-MS/MS mass spectrometer. Different fragmentation energies have been used to ensure the ion marker occurrence in the analyte stereochemistry. It is evident that the collision energies control in structural analysis of molecules provides a powerful and modern analytical tool to be applied in control laboratories.
format article
author Guillermo L. MONTOYA P.
Alejandra RENDÓN M.
Gabriel J. ARANGO A.
author_facet Guillermo L. MONTOYA P.
Alejandra RENDÓN M.
Gabriel J. ARANGO A.
author_sort Guillermo L. MONTOYA P.
title IDENTIFICATION AND DIFFERENTIATION OF UNDERIVATIZED DIASTEROMERIC
title_short IDENTIFICATION AND DIFFERENTIATION OF UNDERIVATIZED DIASTEROMERIC
title_full IDENTIFICATION AND DIFFERENTIATION OF UNDERIVATIZED DIASTEROMERIC
title_fullStr IDENTIFICATION AND DIFFERENTIATION OF UNDERIVATIZED DIASTEROMERIC
title_full_unstemmed IDENTIFICATION AND DIFFERENTIATION OF UNDERIVATIZED DIASTEROMERIC
title_sort identification and differentiation of underivatized diasteromeric
publisher Universidad de Antioquia
publishDate 2010
url https://doaj.org/article/12219e5589e2425d943a60f5d7f84444
work_keys_str_mv AT guillermolmontoyap identificationanddifferentiationofunderivatizeddiasteromeric
AT alejandrarendonm identificationanddifferentiationofunderivatizeddiasteromeric
AT gabrieljarangoa identificationanddifferentiationofunderivatizeddiasteromeric
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