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Novel Ascorbic Acid Co-Crystal Formulations for Improved Stability

A series of co-crystals of ascorbic acid were prepared with equimolar amounts of co-crystal formers (CCFs), including isonicotinic acid, nicotinic acid, 3,4-dihydroxybenzoic acid, 2,5-dihydroxybenzoic acid and m-hydroxybenzoic acid, by slow solvent evaporation and solvent-assisted grinding. The co-c...

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Autores principales: Zhang, Hui, Zeng, Huahui, Li, Mengfei, Song, Yagang, Tian, Shuo, Xiong, Jing, He, Lan, Liu, Yang, Wu, Xiangxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699323/
https://www.ncbi.nlm.nih.gov/pubmed/36432100
http://dx.doi.org/10.3390/molecules27227998
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author Zhang, Hui
Zeng, Huahui
Li, Mengfei
Song, Yagang
Tian, Shuo
Xiong, Jing
He, Lan
Liu, Yang
Wu, Xiangxiang
author_facet Zhang, Hui
Zeng, Huahui
Li, Mengfei
Song, Yagang
Tian, Shuo
Xiong, Jing
He, Lan
Liu, Yang
Wu, Xiangxiang
author_sort Zhang, Hui
collection PubMed
description A series of co-crystals of ascorbic acid were prepared with equimolar amounts of co-crystal formers (CCFs), including isonicotinic acid, nicotinic acid, 3,4-dihydroxybenzoic acid, 2,5-dihydroxybenzoic acid and m-hydroxybenzoic acid, by slow solvent evaporation and solvent-assisted grinding. The co-crystals were characterized by single-crystal X-ray diffraction spectroscopy, powder X-ray diffraction, IR spectroscopy, differential scanning calorimetry and thermogravimetric analysis. Molecular dynamics (MD) simulations further validated the interaction energy and the possible intermolecular hydrogen bonds among VC and CCFs. The co-crystals showed improved stability when exposed to different wavelengths of light, pH and temperatures compared to the free analogue, especially at higher pH (~9) and lower temperature (~4 °C).
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spelling pubmed-96993232022-11-26 Novel Ascorbic Acid Co-Crystal Formulations for Improved Stability Zhang, Hui Zeng, Huahui Li, Mengfei Song, Yagang Tian, Shuo Xiong, Jing He, Lan Liu, Yang Wu, Xiangxiang Molecules Article A series of co-crystals of ascorbic acid were prepared with equimolar amounts of co-crystal formers (CCFs), including isonicotinic acid, nicotinic acid, 3,4-dihydroxybenzoic acid, 2,5-dihydroxybenzoic acid and m-hydroxybenzoic acid, by slow solvent evaporation and solvent-assisted grinding. The co-crystals were characterized by single-crystal X-ray diffraction spectroscopy, powder X-ray diffraction, IR spectroscopy, differential scanning calorimetry and thermogravimetric analysis. Molecular dynamics (MD) simulations further validated the interaction energy and the possible intermolecular hydrogen bonds among VC and CCFs. The co-crystals showed improved stability when exposed to different wavelengths of light, pH and temperatures compared to the free analogue, especially at higher pH (~9) and lower temperature (~4 °C). MDPI 2022-11-18 /pmc/articles/PMC9699323/ /pubmed/36432100 http://dx.doi.org/10.3390/molecules27227998 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
Zhang, Hui
Zeng, Huahui
Li, Mengfei
Song, Yagang
Tian, Shuo
Xiong, Jing
He, Lan
Liu, Yang
Wu, Xiangxiang
Novel Ascorbic Acid Co-Crystal Formulations for Improved Stability
title Novel Ascorbic Acid Co-Crystal Formulations for Improved Stability
title_full Novel Ascorbic Acid Co-Crystal Formulations for Improved Stability
title_fullStr Novel Ascorbic Acid Co-Crystal Formulations for Improved Stability
title_full_unstemmed Novel Ascorbic Acid Co-Crystal Formulations for Improved Stability
title_short Novel Ascorbic Acid Co-Crystal Formulations for Improved Stability
title_sort novel ascorbic acid co-crystal formulations for improved stability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699323/
https://www.ncbi.nlm.nih.gov/pubmed/36432100
http://dx.doi.org/10.3390/molecules27227998
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