Abstract

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.

Highlights

  • Taxifolin, known as dihydroquercetin, possesses several interesting biological properties

  • The results demonstrated the structural richness of Tax, for which six crystalline phases were evidenced

  • Pristine-Tax (100 mg) was dissolved in a minimum volume of each of the following solvents: acetone (AC), acetonitrile (ACN), chloroform:methanol 90:10 (CH-ME), dichloromethane:ethanol 95:5 (DM-ET), ethyl acetate (EA), ethanol (ET), and methanol (ME); these solutions were completely evaporated at 25 ◦ C and 35% relative humidity (RH) in about 1 week under a laboratory fume hood

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Summary

Introduction

Known as dihydroquercetin, possesses several interesting biological properties. Since dissolution kinetics are affected by crystalline form, it is important to investigate the presence of polymorphs obtained following Tax purification/crystallization. It is known that the presence of different crystalline forms can dramatically affect fundamental characteristics of the API such as chemical (reactivity), physical (shape, hygroscopicity, conductivity, density), thermodynamic (free energy, solubility, melting point, vapor pressure, and others), and mechanical (compressibility, friability, hardness, and flux) properties [17–19]. The determination of these features is one of the aims of the preformulation studies during drug development. Preformulation focuses on the physico-chemical properties of a new drug candidate since they influence its performance and the development of the pharmaceutical formulation

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