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通过冷冻透射电子显微镜和三维电子衍射揭示卡马西平结晶的早期阶段。

Revealing the early stages of carbamazepine crystallization by cryoTEM and 3D electron diffraction.

作者信息

Broadhurst Edward T, Xu Hongyi, Parsons Simon, Nudelman Fabio

机构信息

EaStCHEM School of Chemistry and Centre for Science at Extreme Conditions, The University of Edinburgh, King's Buildings, West Mains Road, Edinburgh EH9 3FJ, United Kingdom.

Materials and Environmental Chemistry, Stockholm University, Stockholm, SE-106 91, Sweden.

出版信息

IUCrJ. 2021 Oct 30;8(Pt 6):860-866. doi: 10.1107/S2052252521010101. eCollection 2021 Nov 1.

Abstract

Time-resolved carbamazepine crystallization from wet ethanol has been monitored using a combination of cryoTEM and 3D electron diffraction. Carbamazepine is shown to crystallize exclusively as a dihydrate after 180 s. When the timescale was reduced to 30 s, three further polymorphs could be identified. At 20 s, the development of early stage carbamazepine dihydrate was observed through phase separation. This work reveals two possible crystallization pathways present in this active pharmaceutical ingredient.

摘要

利用低温透射电子显微镜(cryoTEM)和三维电子衍射相结合的方法,监测了卡马西平在湿乙醇中的时间分辨结晶过程。结果表明,180秒后卡马西平仅以二水合物形式结晶。当时间尺度缩短至30秒时,还可识别出另外三种多晶型物。在20秒时,通过相分离观察到了早期卡马西平二水合物的形成。这项工作揭示了这种活性药物成分中存在的两种可能的结晶途径。

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