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用中红外光谱和多曲线分辨率测定共晶相纯度。

Determination of co-crystal phase purity by mid infrared spectroscopy and multiple curve resolution.

机构信息

SSPC Pharmaceutical Research Centre, School of Pharmacy, University College Cork, Cork, Ireland; APC Ltd., Building 11, Cherrywood Business Park, Loughlinstown, Dublin D18 DH50, Ireland.

LAQV/REQUIMTE, Departamento de Ciências Químicas, Faculdade de Farmácia, Universidade do Porto, Rua Jorge Viterbo Ferreira, 228, 4050-313 Porto, Portugal.

出版信息

Int J Pharm. 2021 Feb 15;595:120246. doi: 10.1016/j.ijpharm.2021.120246. Epub 2021 Jan 20.

Abstract

Multivariate Curve Resolution (MCR) was used to determine the phase purity of pharmaceutical co-crystals from mid infrared spectra. An in-silico coformer screening was used to choose one of ten potential coformers. This analysis used quantum chemistry simulation to predict which coformers are thermodynamically inclined to form cocrystals with the model drug, hydrochlorothiazide. The coformer chosen was nicotinamide. An experimental solvent screening by ultrasound assisted slurry co-crystallization was performed to evaluate the capacity of the method to determine phase purity. Afterwards, slurry and slow evaporation co-crystallizations were performed at 10, 25, and 40 °C using 7 solvent systems, and two levels of agitation for the evaporation co-crystallization (on and off). Mid infrared spectroscopy (MIRS) analysis of the products of these co-crystallizations was used to develop an MCR model to determine co-crystal phase purity. The MCR results were compared with a reference co-crystal. Experimental design (DoE) was used to investigate the effect of solvents, temperature, and agitation on the purity of co-crystals produced by slurry and evaporation co-crystallization. DoE revealed that evaporation co-crystallization with agitating at 65 rpm formed co-crystals with greater phase purity. The optimal temperature varied with the solvent used.

摘要

多变量曲线分辨(MCR)用于从中红外光谱确定药物共晶的相纯度。使用虚拟共晶筛选选择十种潜在共晶中的一种。该分析使用量子化学模拟预测哪些共晶更倾向于与模型药物氢氯噻嗪形成共晶。选择的共晶为烟酰胺。通过超声辅助浆态共结晶进行实验溶剂筛选,以评估该方法确定相纯度的能力。然后,在 10、25 和 40°C 下使用 7 种溶剂体系和蒸发共结晶的两个搅拌水平(开和关)进行浆态和缓慢蒸发共结晶。使用中红外光谱(MIRS)分析这些共结晶产物,以开发 MCR 模型来确定共晶的相纯度。将 MCR 结果与参考共晶进行比较。实验设计(DoE)用于研究溶剂、温度和搅拌对浆态和蒸发共结晶生成的共晶纯度的影响。DoE 表明,以 65rpm 搅拌的蒸发共结晶形成了具有更高相纯度的共晶。最佳温度随所用溶剂而变化。

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