Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1784573818197508096 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8469002 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT stengermourafernandacristina exploringtaxifolinpolymorphsinsightsonhydrateandanhydrousforms AT pinnanicola exploringtaxifolinpolymorphsinsightsonhydrateandanhydrousforms AT vivaniriccardo exploringtaxifolinpolymorphsinsightsonhydrateandanhydrousforms AT nunesgiseleelias exploringtaxifolinpolymorphsinsightsonhydrateandanhydrousforms AT schoubbenaurelie exploringtaxifolinpolymorphsinsightsonhydrateandanhydrousforms AT bellebresolintaniamari exploringtaxifolinpolymorphsinsightsonhydrateandanhydrousforms AT becholdivanhelmuth exploringtaxifolinpolymorphsinsightsonhydrateandanhydrousforms AT riccimaurizio exploringtaxifolinpolymorphsinsightsonhydrateandanhydrousforms |