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Near infrared spectroscopy for blend uniformity monitoring: An innovative qualitative application based on the coefficient of determination

机译:用于混合物均匀性监测的近红外光谱:基于决定系数的创新定性应用

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Blending process is a critical unit operation in the pharmaceutical industry during the solid dosage form production. Near infrared (NIR) spectroscopy is a powerful analytical tool to assess the blend homogeneity in real-time. In this paper, a new methodology for blending process monitoring and for end point confirmation is proposed. Quantitative procedure validation and maintenance of NIR procedures are time-consuming activities that can prevent the adoption of PAT tools in the pharmaceutical industry. Clearly, there is a need in the industry for simpler and more intuitive qualitative blendmonitoring analytical procedure that are easy to build, validate and maintain. The method introduced herein consists of tracking the trend of the Coefficient of Determination (CD) between a mean reference spectrum from a homogeneous batch and the NIR spectra that are recorded during the blending operation. Four formulations of commercial products were selected from different scales-including low dosage solid form-to show the usefulness of the method. In addition, this analytical procedure is tested with data from two different types of spectrometers (diode array instruments). Method calibration was performed with five batches (representing expected process variability) for each product: one for the computation of the homogeneous batch target spectrum and four to compute the limit of the CD values related to anticipated and acceptable homogeneity. Method validation was performed with homogeneous batches and with challenge spectra for assessing the specificity of the method. Real-world examples (e.g. technical, validation batches and clinical batches) were presented in order to demonstrate that this method is able to detect inhomogeneous batches. The new qualitative method presented in this paper is useful for determination of the blending endpoint, in assessing the blend uniformity in real-time and in increasing process understanding during early development and troubleshooting.
机译:混合过程是制药行业固体剂型生产过程中的关键单元操作。近红外 (NIR) 光谱是一种强大的分析工具,可以实时评估混合物的均匀性。该文提出了一种混合过程监控和终点确认的新方法。NIR 程序的定量程序验证和维护是一项耗时的活动,可能会阻碍制药行业采用 PAT 工具。显然,该行业需要更简单、更直观、易于构建、验证和维护的定性混合监测分析程序。本文介绍的方法包括跟踪来自均质批次的平均参考光谱与混合操作期间记录的近红外光谱之间的决定系数 (CD) 趋势。从不同尺度(包括低剂量固体形式)中筛选出4种商业产品配方,以显示该方法的实用性。此外,该分析程序还使用来自两种不同类型的光谱仪(二极管阵列仪器)的数据进行测试。对每种产品进行方法校准,使用五个批次(代表预期的过程变异性):一个用于计算均质批次目标光谱,四个用于计算与预期和可接受的均匀性相关的CD值限值。使用均质批次和挑战谱进行方法验证,以评估方法的特异性。为了证明该方法能够检测不均匀的批次,提供了真实世界的例子(例如技术批次、验证批次和临床批次)。本文提出的新的定性方法可用于确定混合终点,实时评估混合均匀性,并在早期开发和故障排除过程中增加对工艺的理解。

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