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使用拉曼光谱法在线监测湿法制粒过程中的水合物形成。

In-line monitoring of hydrate formation during wet granulation using Raman spectroscopy.

作者信息

Wikström Håkan, Marsac Patrick J, Taylor Lynne S

机构信息

Industrial and Physical Pharmacy, School of Pharmacy, Purdue University, West Lafayette, Indiana 47907, USA.

出版信息

J Pharm Sci. 2005 Jan;94(1):209-19. doi: 10.1002/jps.20241.

Abstract

Process-induced transformations are very important to control during pharmaceutical manufacturing because they may change the properties of the active pharmaceutical ingredient in the drug product, compromising therapeutic efficacy. One process that may facilitate a process-induced transformation is high-shear wet granulation. In this study, the feasibility of Raman spectroscopy for in-line monitoring of the transformation of theophylline anhydrous to theophylline monohydrate during high-shear wet granulation has been evaluated. The midpoint of conversion occurred 3 min after the binder solution was added. The effects of several processing parameters were also examined, including mixing speed and monohydrate seeding. Mixing speed had the greatest effect on the transformation, where an increase in mixing speed shortened the onset time and increased the rate of transformation. In contrast, seeding with monohydrate or changing the way in which the binder was incorporated into the granules did not affect the transformation profile. The transformation kinetics observed during wet granulation were compared with those generated by a simple model describing the solvent-mediated transformation of theophylline in solution. In conclusion, these studies show that Raman spectroscopy can be used for in-line monitoring of solid-state transformations during wet granulation. In addition, for this particular compound, a simple solvent-mediated transformation model has been shown to be useful for estimating the time scale for hydrate formation during high-shear wet granulation.

摘要

在药物制造过程中,控制工艺诱导的转变非常重要,因为它们可能会改变药品中活性药物成分的性质,从而损害治疗效果。高剪切湿法制粒是一种可能促进工艺诱导转变的工艺。在本研究中,评估了拉曼光谱在线监测高剪切湿法制粒过程中无水茶碱向一水合茶碱转变的可行性。转变的中点在加入粘合剂溶液后3分钟出现。还研究了几个工艺参数的影响,包括混合速度和一水合物晶种。混合速度对转变的影响最大,混合速度的增加缩短了起始时间并提高了转变速率。相比之下,加入一水合物晶种或改变粘合剂加入颗粒的方式对转变过程没有影响。将湿法制粒过程中观察到的转变动力学与一个描述溶液中茶碱溶剂介导转变的简单模型所产生的动力学进行了比较。总之,这些研究表明拉曼光谱可用于在线监测湿法制粒过程中的固态转变。此外,对于这种特定的化合物,一个简单的溶剂介导转变模型已被证明可用于估计高剪切湿法制粒过程中水合物形成的时间尺度。

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