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Environmentally Sustainable Achiral and Chiral Chromatographic Analysis of Amino Acids in Food Supplements

Two LC methods were developed for the achiral and chiral reversed-phase (RP) analysis of an amino acid (AA) pool in a food supplement, in compliance with the main paradigms of Green Chromatography. A direct achiral ion-pairing RP-HPLC method was optimized under gradient conditions with a water-ethan...

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Autores principales: Varfaj, Ina, Carotti, Andrea, Mangiapelo, Luciano, Cossignani, Lina, Taticchi, Agnese, Macchiarulo, Antonio, Ianni, Federica, Sardella, Roccaldo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9697624/
https://www.ncbi.nlm.nih.gov/pubmed/36431824
http://dx.doi.org/10.3390/molecules27227724
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author Varfaj, Ina
Carotti, Andrea
Mangiapelo, Luciano
Cossignani, Lina
Taticchi, Agnese
Macchiarulo, Antonio
Ianni, Federica
Sardella, Roccaldo
author_facet Varfaj, Ina
Carotti, Andrea
Mangiapelo, Luciano
Cossignani, Lina
Taticchi, Agnese
Macchiarulo, Antonio
Ianni, Federica
Sardella, Roccaldo
author_sort Varfaj, Ina
collection PubMed
description Two LC methods were developed for the achiral and chiral reversed-phase (RP) analysis of an amino acid (AA) pool in a food supplement, in compliance with the main paradigms of Green Chromatography. A direct achiral ion-pairing RP-HPLC method was optimized under gradient conditions with a water-ethanol (EtOH) eluent containing heptafluorobutyric acid (0.1%, v/v), to quantify the eight essential AAs (Ile, Leu, Lys, Met, Phe, Thr, Trp, and Val) contained in the food supplement. Thus, the usually employed acetonitrile was profitably substituted with the less toxic and more benign EtOH. The method was validated for Leu and Phe. The chiral LC method performed with a teicoplanin chiral stationary phase was developed with a water-EtOH (60:40, v/v) eluent with 0.1%, v/v acetic acid. The enantioselective analysis was carried out without any prior derivatization step. Both developed methods performed highly for all eight AAs and revealed that: (i) the content of six out of eight AAs was consistent with the manufacturer declaration; (ii) only L-AAs were present. Furthermore, it was demonstrated that a two-dimensional achiral–chiral configuration is possible in practice, making it even more environmentally sustainable. A molecular modelling investigation revealed interesting insights into the enantiorecognition mechanism of Lys.
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spelling pubmed-96976242022-11-26 Environmentally Sustainable Achiral and Chiral Chromatographic Analysis of Amino Acids in Food Supplements Varfaj, Ina Carotti, Andrea Mangiapelo, Luciano Cossignani, Lina Taticchi, Agnese Macchiarulo, Antonio Ianni, Federica Sardella, Roccaldo Molecules Article Two LC methods were developed for the achiral and chiral reversed-phase (RP) analysis of an amino acid (AA) pool in a food supplement, in compliance with the main paradigms of Green Chromatography. A direct achiral ion-pairing RP-HPLC method was optimized under gradient conditions with a water-ethanol (EtOH) eluent containing heptafluorobutyric acid (0.1%, v/v), to quantify the eight essential AAs (Ile, Leu, Lys, Met, Phe, Thr, Trp, and Val) contained in the food supplement. Thus, the usually employed acetonitrile was profitably substituted with the less toxic and more benign EtOH. The method was validated for Leu and Phe. The chiral LC method performed with a teicoplanin chiral stationary phase was developed with a water-EtOH (60:40, v/v) eluent with 0.1%, v/v acetic acid. The enantioselective analysis was carried out without any prior derivatization step. Both developed methods performed highly for all eight AAs and revealed that: (i) the content of six out of eight AAs was consistent with the manufacturer declaration; (ii) only L-AAs were present. Furthermore, it was demonstrated that a two-dimensional achiral–chiral configuration is possible in practice, making it even more environmentally sustainable. A molecular modelling investigation revealed interesting insights into the enantiorecognition mechanism of Lys. MDPI 2022-11-09 /pmc/articles/PMC9697624/ /pubmed/36431824 http://dx.doi.org/10.3390/molecules27227724 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Varfaj, Ina
Carotti, Andrea
Mangiapelo, Luciano
Cossignani, Lina
Taticchi, Agnese
Macchiarulo, Antonio
Ianni, Federica
Sardella, Roccaldo
Environmentally Sustainable Achiral and Chiral Chromatographic Analysis of Amino Acids in Food Supplements
title Environmentally Sustainable Achiral and Chiral Chromatographic Analysis of Amino Acids in Food Supplements
title_full Environmentally Sustainable Achiral and Chiral Chromatographic Analysis of Amino Acids in Food Supplements
title_fullStr Environmentally Sustainable Achiral and Chiral Chromatographic Analysis of Amino Acids in Food Supplements
title_full_unstemmed Environmentally Sustainable Achiral and Chiral Chromatographic Analysis of Amino Acids in Food Supplements
title_short Environmentally Sustainable Achiral and Chiral Chromatographic Analysis of Amino Acids in Food Supplements
title_sort environmentally sustainable achiral and chiral chromatographic analysis of amino acids in food supplements
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9697624/
https://www.ncbi.nlm.nih.gov/pubmed/36431824
http://dx.doi.org/10.3390/molecules27227724
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