Exploring Taxifolin Polymorphs: Insights on Hydrate and Anhydrous Forms
| Autor: | Fernanda Cristina Stenger Moura, Nicola Pinna, Riccardo Vivani, Gisele Elias Nunes, Aurélie Schoubben, Tania Mari Bellé Bresolin, Ivan Helmuth Bechold, Maurizio Ricci |
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| Jazyk: | angličtina |
| Rok vydání: | 2021 |
| Předmět: | |
| Zdroj: | Pharmaceutics, Vol 13, Iss 9, p 1328 (2021) |
| Druh dokumentu: | article |
| ISSN: | 13091328 1999-4923 |
| DOI: | 10.3390/pharmaceutics13091328 |
| Popis: | 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. |
| Databáze: | Directory of Open Access Journals |
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