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西他列汀磷酸盐一水合物和无水物 II 向新型无水物 IV 的固态相转变——溶剂驱动、温度诱导和应力测试。

Solid-State Phase Transformation of Monohydrate and Anhydrous Form II of Sitagliptin Phosphate into a Novel Anhydrous Form IV - Solvent-Driven, Temperature-Induced and Stress Testings.

机构信息

Research and Development, Alkaloid AD, Bul. Aleksandar Makedonski 12, 1000 Skopje, North Macedonia.

Department of Chemistry, Southern Methodist University, 231 Fondren Science Building, Dallas, TX 75275, USA.

出版信息

J Pharm Sci. 2024 Feb;113(2):396-406. doi: 10.1016/j.xphs.2023.11.007. Epub 2023 Nov 14.

Abstract

The solid form landscape of sitagliptin phosphate was systematically evaluated by differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy and X-ray powder diffraction (XRPD), supported by a plethora of auxiliary analytical techniques. The preformulation experiments resulted in the transition of sitagliptin phosphate monohydrate into a new anhydrous form (designated as form IV), obtained after recrystallization from absolute ethanol. The anhydrous form IV remained stable under stressed conditions (1 month at 25 °C/60 %RH and 40 °C/75 %RH). On the other hand, thermal heating (dehydration) of sitagliptin phosphate monohydrate resulted in conversion into another anhydrous form II. Form II was found to be metastable, because after melting, under exposure at 40 °C/75 %RH for 1 month, or when dissolved in absolute ethanol converted to the stable anhydrous form IV of sitagliptin phosphate. A monotropic relationship was found between both studied anhydrous forms. Intrinsic dissolution tests revealed differences in the dissolution rates between the monohydrate and the anhydrous forms of sitagliptin phosphate. This research corrects the record with an accurate chemical composition of the anhydrous form IV of sitagliptin phosphate that was previously regarded as a hemiethanolate. In addition, the crystal structure of anhydrous form II of sitagliptin phosphate has been solved and reported for the first time.

摘要

磷酸西他列汀的固体形态景观通过差示扫描量热法(DSC)、热重分析(TGA)、傅里叶变换红外光谱(FTIR)、拉曼光谱和 X 射线粉末衍射(XRPD)进行了系统评估,辅以多种辅助分析技术。制剂前研究导致磷酸西他列汀一水合物向新的无水形式(指定为形式 IV)转变,通过从无水乙醇重结晶获得。无水形式 IV 在压力条件下保持稳定(在 25°C/60%RH 和 40°C/75%RH 下放置 1 个月)。另一方面,磷酸西他列汀一水合物的热加热(脱水)导致其转化为另一种无水形式 II。发现形式 II 是亚稳定的,因为在熔化后,在 40°C/75%RH 下暴露 1 个月,或者当溶解在无水乙醇中时,会转化为稳定的无水形式 IV。研究发现两种研究无水形式之间存在单型关系。内在溶解测试显示磷酸西他列汀一水合物和无水形式之间的溶解速率存在差异。这项研究纠正了以前被认为是半乙醇酸盐的磷酸西他列汀无水形式 IV 的准确化学成分记录。此外,还首次解决并报告了磷酸西他列汀无水形式 II 的晶体结构。

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