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>Polymorph Transformation in Paracetamol Monitored by In-line NIR Spectroscopy During a Cooling Crystallization Process
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Polymorph Transformation in Paracetamol Monitored by In-line NIR Spectroscopy During a Cooling Crystallization Process
The reliable in-line monitoring of pharmaceutical processes has been regarded as a key tool toward the full implementation of process analytical technology. In this study, near-infrared (NIR) spectroscopy was examined for use as an in-line monitoring method of the paracetamol cooling crystallization process. The drug powder was dissolved in ethanol-based cosolvent at 60°C and was cooled by 1°C/min for crystallization. NIR spectra acquired by in-line measurement were interpreted by principal component analysis combined with off-line characterizations via X-ray diffraction, optical microscopy, and transmission electron microscopy. The whole crystallization process appeared to take place in three steps. A metastable form II polymorph of paracetamol was formed and transformed into the stable form I polymorph on the way to the growth of pure form I by cooling crystallization. These observations are consistent with a previous focused beam reflectance method-based study (Barthe et al., Cryst Growth Des 8:3316–3322, ).
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机译:可靠的制药过程在线监测被视为全面实施过程分析技术的关键工具。在这项研究中,检查了近红外(NIR)光谱作为对乙酰氨基酚冷却结晶过程的在线监测方法。将药物粉末在60℃溶解在乙醇基助溶剂中,并以1℃/ min的速度冷却以结晶。通过主成分分析结合离线表征,通过X射线衍射,光学显微镜和透射电子显微镜对通过在线测量获得的NIR光谱进行解释。整个结晶过程似乎分三步进行。形成了扑热息痛的亚稳态II型多晶型物,并在通过冷却结晶生长纯I型的过程中转变为稳定的I型多晶型物。这些观察结果与以前基于聚焦光束反射法的研究相一致(Barthe等人,Cryst Growth Des 8:3316–3322,)。
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