Chiral and achiral separation of ten flavanones using supercritical fluid chromatography. Application to bee pollen analysis.


Journal

Journal of chromatography. A
ISSN: 1873-3778
Titre abrégé: J Chromatogr A
Pays: Netherlands
ID NLM: 9318488

Informations de publication

Date de publication:
06 Dec 2022
Historique:
received: 01 07 2022
revised: 28 10 2022
accepted: 30 10 2022
pubmed: 15 11 2022
medline: 30 11 2022
entrez: 14 11 2022
Statut: ppublish

Résumé

The separation of ten flavanones (flavanone, 2'-hydroxyflavanone, 4'-hydroxyflavanone, 6-hydroxyflavanone, 7-hydroxyflavanone, naringenin, naringin, hesperetin, pinostrobin, and taxifolin) using supercritical fluid chromatography and considering achiral and chiral approaches has been studied in this work. For this purpose, different stationary phases and organic modifiers have been checked. Considering the achiral separation, the best results were obtained with the Lichrospher 100 Diol column at 35 °C, 3 mL/min, 150 bar and a gradient of 2-propanol from 5% to 50%. The baseline separation of the ten compounds was achieved in 18 min. Using the chiral column Chiralpak AD, the separation of the ten pairs of enantiomers was obtained in 32 min. In this case, the chromatographic conditions were 30 °C, 3 mL/min, 150 bar and the organic modifier was a mixture ethanol/methanol (80:20) containing 0.1% of trifluoroacetic acid applied in an elution gradient from 15% to 50%. The applicability of the proposed chiral method was assessed by analysing bee pollen samples and 2S-pinostrobin was determined in some of them.

Identifiants

pubmed: 36375216
pii: S0021-9673(22)00824-X
doi: 10.1016/j.chroma.2022.463633
pii:
doi:

Substances chimiques

Flavanones 0
Methanol Y4S76JWI15

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

463633

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Ana M Ares (AM)

Department of Analytical Chemistry, Faculty of Sciences, I. U. CINQUIMA, Analytical Chemistry Group (TESEA), University of Valladolid, C/ Paseo de Belén 5, Valladolid E-47011, Spain.

José Bernal (J)

Department of Analytical Chemistry, Faculty of Sciences, I. U. CINQUIMA, Analytical Chemistry Group (TESEA), University of Valladolid, C/ Paseo de Belén 5, Valladolid E-47011, Spain.

Andrea Janvier (A)

Department of Analytical Chemistry, Faculty of Sciences, I. U. CINQUIMA, Analytical Chemistry Group (TESEA), University of Valladolid, C/ Paseo de Belén 5, Valladolid E-47011, Spain.

Laura Toribio (L)

Department of Analytical Chemistry, Faculty of Sciences, I. U. CINQUIMA, Analytical Chemistry Group (TESEA), University of Valladolid, C/ Paseo de Belén 5, Valladolid E-47011, Spain. Electronic address: ltoribio@uva.es.

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Classifications MeSH