固溶体形成法捕获BI 763963的溶剂

IF 3.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Samruddhi Patil, Tao Zhang, Brian Linehan, Vincent Abeyta and Fredrik L. Nordstrom*, 
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引用次数: 0

摘要

确定了终止候选药物BI 763963的溶剂包封机制。通过实验方法和结构分析相结合,证明了乙醇(EtOH)和异丙醇(IPA)通过固溶体的形式被包裹在BI 763963的晶格中。构建了两个二元T-w相图,显示了BI 763963的固相和液相的轮廓,其中EtOH和IPA分别以0.54%和1.5 wt %的平衡态存在于BI 763963的固相中。重要的是,BI 763963的溶剂溶解度被发现依赖于固相中的残留溶剂水平,在EtOH的情况下,仅在1.1 wt %的EtOH夹持下,溶剂溶解度增加了近50%。从工业加工和活性药物成分(API)的药学性质方面讨论了残留溶剂对溶剂溶解度的影响。在EtOH和IPA中对BI 763963进行了不同过饱和比的再结晶实验。越高的过饱和度产生越高的溶剂包载,在两种溶剂中,溶剂包载随原料药收率线性降低。讨论了这些趋势,并将其与以前的研究结果进行了比较,这些结果显示了由于固溶体的结晶成核而出现的类似行为。采用溶剂包埋的溶解度增强效应来确定结晶过程中的实际过饱和比。分析表明,当假设固相是纯的,或者原料药的溶解度与被包裹的溶剂无关时,过饱和比误差可达55%。最后,讨论了工业减缓措施,以减少基于固溶体形成的残余溶剂水平。实验证明,其他固态可混相杂质可以完全改变体系的相平衡,导致IPA含量从2.2 wt %降低到0.86 wt %。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Solvent Entrapment of BI 763963 by Solid Solution Formation

Solvent Entrapment of BI 763963 by Solid Solution Formation

The underlying mechanism for solvent entrapment has been determined for terminated drug candidate BI 763963. Ethanol (EtOH) and isopropanol (IPA) were entrapped in the crystal lattice of BI 763963 through solid solution formation, as demonstrated through a combination of experimental methods and structural analysis. Two binary T-w phase diagrams were constructed showing the outline of the solidus and liquidus, where EtOH and IPA are present in the solid phase of BI 763963 at 0.54 and 1.5 wt %, respectively, at equilibrium. Importantly, the solvent solubility of BI 763963 was found to be dependent on the residual solvent level in the solid phase and in the case of EtOH increased by almost 50% at just 1.1 wt % EtOH entrapment. The implications of the effect of residual solvents on solvent solubility are discussed with respect to industrial processing and the pharmaceutical properties of the active pharmaceutical ingredient (API). Furthermore, recrystallization experiments were carried out on BI 763963 at different supersaturation ratios in both EtOH and IPA. Higher supersaturation yielded higher solvent entrapment initially, which in both solvents decreased linearly with API yield. The trends are discussed and compared to previous contributions showing similar behavior that appeared due to crystal nucleation of a solid solution. The solubility-enhancing effect from solvent entrapment is used to determine the actual supersaturation ratio during crystallization. The analysis shows that errors up to 55% in the supersaturation ratio can be introduced when assuming that the solid phase is pure or that the solubility of an API is independent of entrapped solvent. Finally, industrial mitigation measures are discussed to reduce residual solvent levels based on solid solution formation. It is demonstrated experimentally that other solid-state miscible impurities can completely alter the phase equilibria of the system, leading in one example to a reduction in IPA content from 2.2 to 0.86 wt %.

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来源期刊
Crystal Growth & Design
Crystal Growth & Design 化学-材料科学:综合
CiteScore
6.30
自引率
10.50%
发文量
650
审稿时长
1.9 months
期刊介绍: The aim of Crystal Growth & Design is to stimulate crossfertilization of knowledge among scientists and engineers working in the fields of crystal growth, crystal engineering, and the industrial application of crystalline materials. Crystal Growth & Design publishes theoretical and experimental studies of the physical, chemical, and biological phenomena and processes related to the design, growth, and application of crystalline materials. Synergistic approaches originating from different disciplines and technologies and integrating the fields of crystal growth, crystal engineering, intermolecular interactions, and industrial application are encouraged.
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