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Preferential crystallization for the purification of similar hydrophobic polyphenols

BACKGROUND: Preferential crystallization is a common technique used in the purification of enantiomers, proving that crystallization may also be applied to the purification of very similar molecules by seeding the solution with the desired compound. Nonetheless, its application to other organic mole...

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Detalles Bibliográficos
Autores principales: Silva, Marcelo, Vieira, Briana, Ottens, Marcel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033112/
https://www.ncbi.nlm.nih.gov/pubmed/30008507
http://dx.doi.org/10.1002/jctb.5526
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author Silva, Marcelo
Vieira, Briana
Ottens, Marcel
author_facet Silva, Marcelo
Vieira, Briana
Ottens, Marcel
author_sort Silva, Marcelo
collection PubMed
description BACKGROUND: Preferential crystallization is a common technique used in the purification of enantiomers, proving that crystallization may also be applied to the purification of very similar molecules by seeding the solution with the desired compound. Nonetheless, its application to other organic molecules is less widely documented in the literature. Knowing that chemically related polyphenols are generally co‐produced by fermentation and their purification can be too expensive for their market value, this technique may contribute to developing a downstream process with less expensive steps. The goal of this work is to show the applicability of the preferential crystallization concept to the purification of similar polyphenols – naringenin and trans‐resveratrol – with either single or coupled crystallizers. RESULTS: After developing the required crystallization kinetic models, an experiment using two coupled vessels was devised, where a 63% yield of naringenin and 44% yield of trans‐resveratrol was obtained, with ≥98% purity in both cases. When the vessels were working independently, 81% of pure trans‐resveratrol (started 60% pure) and 70% of pure naringenin (started 68% pure) were recovered. CONCLUSION: The experiments performed show the possibility of separately purifying two similar molecules (from 60% to roughly 100%) with promising yields, despite their similar solubility. This method, which can be significantly improved, might provide an economically attractive way for the production of low added value products. © 2017 The Authors. Journal of Chemical Technology & Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.
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spelling pubmed-60331122018-07-12 Preferential crystallization for the purification of similar hydrophobic polyphenols Silva, Marcelo Vieira, Briana Ottens, Marcel J Chem Technol Biotechnol Research Articles BACKGROUND: Preferential crystallization is a common technique used in the purification of enantiomers, proving that crystallization may also be applied to the purification of very similar molecules by seeding the solution with the desired compound. Nonetheless, its application to other organic molecules is less widely documented in the literature. Knowing that chemically related polyphenols are generally co‐produced by fermentation and their purification can be too expensive for their market value, this technique may contribute to developing a downstream process with less expensive steps. The goal of this work is to show the applicability of the preferential crystallization concept to the purification of similar polyphenols – naringenin and trans‐resveratrol – with either single or coupled crystallizers. RESULTS: After developing the required crystallization kinetic models, an experiment using two coupled vessels was devised, where a 63% yield of naringenin and 44% yield of trans‐resveratrol was obtained, with ≥98% purity in both cases. When the vessels were working independently, 81% of pure trans‐resveratrol (started 60% pure) and 70% of pure naringenin (started 68% pure) were recovered. CONCLUSION: The experiments performed show the possibility of separately purifying two similar molecules (from 60% to roughly 100%) with promising yields, despite their similar solubility. This method, which can be significantly improved, might provide an economically attractive way for the production of low added value products. © 2017 The Authors. Journal of Chemical Technology & Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry. John Wiley & Sons, Ltd 2018-01-31 2018-07 /pmc/articles/PMC6033112/ /pubmed/30008507 http://dx.doi.org/10.1002/jctb.5526 Text en © 2017 The Authors. Journal of Chemical Technology & Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Silva, Marcelo
Vieira, Briana
Ottens, Marcel
Preferential crystallization for the purification of similar hydrophobic polyphenols
title Preferential crystallization for the purification of similar hydrophobic polyphenols
title_full Preferential crystallization for the purification of similar hydrophobic polyphenols
title_fullStr Preferential crystallization for the purification of similar hydrophobic polyphenols
title_full_unstemmed Preferential crystallization for the purification of similar hydrophobic polyphenols
title_short Preferential crystallization for the purification of similar hydrophobic polyphenols
title_sort preferential crystallization for the purification of similar hydrophobic polyphenols
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033112/
https://www.ncbi.nlm.nih.gov/pubmed/30008507
http://dx.doi.org/10.1002/jctb.5526
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