Solubility analysis of venlafaxine hydrochloride polymorphs by shake-flask method and real time monitoring

溶解度 溶解 过饱和度 拉曼光谱 化学 溶解度平衡 粉末衍射 色谱法 分析化学(期刊) 结晶 结晶学 物理化学 有机化学 物理 光学
作者
Krisztina Takács‐Novák,Dóra Tempfli,Dóra Csicsák,Gergely Völgyi,Enikő Borbás,Zsombor Kristóf Nagy,Bálint Sinkó
出处
期刊:Acta pharmaceutica Hungarica [Acta Pharmaceutica Hungarica]
卷期号:89 (2): 88-96 被引量:3
标识
DOI:10.33892/aph.2019.89.88-96
摘要

Aims: The aqueous solubility of two polymorphic forms of venlafaxine hydrochloride was investigated. Methods: The pH-dependent solubility (SpH) over a wide pH range was measured by saturation shake-flask (SSF) method at 25 °C. The solubility of the free base form was depicted by the intrinsic solubility (So). To identify the solid form present at the solubility equilibrium, X-ray powder diffraction (XRPD) and Raman spectroscopy was carried out. The dissolution was studied using real time concentration monitoring applying fiber optic UV probes. Results: No difference was found in the SpH values of Form I and Form II, in the pH range 7.5-12. Solid phase isolated from pH 10-12 suspensions was identified as free base by XRPD and Raman spectroscopy. Precipitates separated from pH 7-8 samples were also identical product. The transition of polymorphs to the free base was supported by the real time dissolution analysis. Conclusion: In this study we demonstrated a good agreement of equilibrium solubility measured by SSF method and in-situ UV fiber optic method. µDISS ProfilerTM has the advantage to provide much more information about dissolution process; with this approach the dissolution kinetic, the supersaturation and the time needed to reach the equilibrium can be easily monitored.

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