A Study of the Changes During Heating of Paracetamol

单斜晶系 成核 再结晶(地质) 结晶 正交晶系 材料科学 升华(心理学) 溶解 结晶习性 过冷 差示扫描量热法 偏振光显微镜 结晶学 化学工程 热力学 化学 晶体结构 有机化学 光学 心理治疗师 古生物学 工程类 物理 生物 心理学
作者
F. N. de Wet,J. J. Gerber,A. P. Lötter,J. G. van der Watt,Theo G. Dekker
出处
期刊:Drug Development and Industrial Pharmacy [Informa]
卷期号:24 (5): 447-453 被引量:22
标识
DOI:10.3109/03639049809085642
摘要

The orthorhombic form of paracetamol has been shown to exhibit greater compressibility and faster dissolution than the monoclinic form. The orthorhombic form is produced by melting of monoclinic crystals of paracetamol followed by cooling at specific rates. Cooling rate, although a very important factor, is not the only factor influencing the formation of either of the two morphs. To study the cooling rate required for production of form II, paracetamol samples were melted in a differential scanning calorimeter, cooled at three specific rates, and melted again. In all of the samples, cooling resulted in the glassy form followed by recrystallization and the melting of form II. On the hot-stage microscope both forms were produced in one sample. Standardizing conditions for prediction of the resulting form remains a problem. There seems to be a great deal of overlap of the two forms' transition phases, which would make it difficult to force the crystallization of one form by keeping the solution or melt at a specific temperature. The thermal behavior of paracetamol during the heating and cooling phases must be understood in order to manipulate the process. A video camera mounted on a hot-stage microscope was used to follow the changes during heating and cooling of both forms. Nucleation, crystal growth, habit transformation, sublimation, and the final melt are shown on snap shots taken from the video.

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