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Exploring Taxifolin Polymorphs: Insights on Hydrate and Anhydrous Forms

Taxifolin, also known as dihydroquercetin, possesses several interesting biological properties. The purpose of the study was to identify polymorphs of taxifolin prepared using crystallization in different solvents. Data from X-ray powder diffraction, differential scanning calorimetry, and thermograv...

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Autores principales: Stenger Moura, Fernanda Cristina, Pinna, Nicola, Vivani, Riccardo, Nunes, Gisele Elias, Schoubben, Aurélie, Bellé Bresolin, Tania Mari, Bechold, Ivan Helmuth, Ricci, Maurizio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469002/
https://www.ncbi.nlm.nih.gov/pubmed/34575404
http://dx.doi.org/10.3390/pharmaceutics13091328
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author Stenger Moura, Fernanda Cristina
Pinna, Nicola
Vivani, Riccardo
Nunes, Gisele Elias
Schoubben, Aurélie
Bellé Bresolin, Tania Mari
Bechold, Ivan Helmuth
Ricci, Maurizio
author_facet Stenger Moura, Fernanda Cristina
Pinna, Nicola
Vivani, Riccardo
Nunes, Gisele Elias
Schoubben, Aurélie
Bellé Bresolin, Tania Mari
Bechold, Ivan Helmuth
Ricci, Maurizio
author_sort Stenger Moura, Fernanda Cristina
collection PubMed
description Taxifolin, also known as dihydroquercetin, possesses several interesting biological properties. The purpose of the study was to identify polymorphs of taxifolin prepared using crystallization in different solvents. Data from X-ray powder diffraction, differential scanning calorimetry, and thermogravimetry enabled us to detect six different crystalline phases for taxifolin. Besides the already known fully hydrated phase, one partially hydrated phase, one monohydrated phase, two anhydrous polymorphs, and one probably solvated phase were obtained. The unit cell parameters were defined for three of them, while one anhydrous polymorph was fully structurally characterized by X-ray powder diffraction data. Scanning electron microscopy and hot stage microscopy were also employed to characterize the crystallized taxifolin powders. The hydrate and anhydrous forms showed remarkable stability in drastic storage conditions, and their solubility was deeply evaluated. The anhydrous form converted into the hydrate form during the equilibrium solubility study and taxifolin equilibrium solubility was about 1.2 mg/mL. The hydrate taxifolin intrinsic dissolution rate was 56.4 μg cm(−2) min(−1). Using Wood’s apparatus, it was not possible to determine the intrinsic dissolution rate of anhydrous taxifolin that is expected to solubilize more rapidly than the hydrate form. In view of its high stability, its use can be hypothesized.
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spelling pubmed-84690022021-09-27 Exploring Taxifolin Polymorphs: Insights on Hydrate and Anhydrous Forms Stenger Moura, Fernanda Cristina Pinna, Nicola Vivani, Riccardo Nunes, Gisele Elias Schoubben, Aurélie Bellé Bresolin, Tania Mari Bechold, Ivan Helmuth Ricci, Maurizio Pharmaceutics Article Taxifolin, also known as dihydroquercetin, possesses several interesting biological properties. The purpose of the study was to identify polymorphs of taxifolin prepared using crystallization in different solvents. Data from X-ray powder diffraction, differential scanning calorimetry, and thermogravimetry enabled us to detect six different crystalline phases for taxifolin. Besides the already known fully hydrated phase, one partially hydrated phase, one monohydrated phase, two anhydrous polymorphs, and one probably solvated phase were obtained. The unit cell parameters were defined for three of them, while one anhydrous polymorph was fully structurally characterized by X-ray powder diffraction data. Scanning electron microscopy and hot stage microscopy were also employed to characterize the crystallized taxifolin powders. The hydrate and anhydrous forms showed remarkable stability in drastic storage conditions, and their solubility was deeply evaluated. The anhydrous form converted into the hydrate form during the equilibrium solubility study and taxifolin equilibrium solubility was about 1.2 mg/mL. The hydrate taxifolin intrinsic dissolution rate was 56.4 μg cm(−2) min(−1). Using Wood’s apparatus, it was not possible to determine the intrinsic dissolution rate of anhydrous taxifolin that is expected to solubilize more rapidly than the hydrate form. In view of its high stability, its use can be hypothesized. MDPI 2021-08-25 /pmc/articles/PMC8469002/ /pubmed/34575404 http://dx.doi.org/10.3390/pharmaceutics13091328 Text en © 2021 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
Stenger Moura, Fernanda Cristina
Pinna, Nicola
Vivani, Riccardo
Nunes, Gisele Elias
Schoubben, Aurélie
Bellé Bresolin, Tania Mari
Bechold, Ivan Helmuth
Ricci, Maurizio
Exploring Taxifolin Polymorphs: Insights on Hydrate and Anhydrous Forms
title Exploring Taxifolin Polymorphs: Insights on Hydrate and Anhydrous Forms
title_full Exploring Taxifolin Polymorphs: Insights on Hydrate and Anhydrous Forms
title_fullStr Exploring Taxifolin Polymorphs: Insights on Hydrate and Anhydrous Forms
title_full_unstemmed Exploring Taxifolin Polymorphs: Insights on Hydrate and Anhydrous Forms
title_short Exploring Taxifolin Polymorphs: Insights on Hydrate and Anhydrous Forms
title_sort exploring taxifolin polymorphs: insights on hydrate and anhydrous forms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469002/
https://www.ncbi.nlm.nih.gov/pubmed/34575404
http://dx.doi.org/10.3390/pharmaceutics13091328
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