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使用多系列近红外高光谱成像和多元曲线分辨技术监测片剂表面的多种固态转变。

Monitoring of multiple solid-state transformations at tablet surfaces using multi-series near-infrared hyperspectral imaging and multivariate curve resolution.

作者信息

Alexandrino Guilherme L, Khorasani Milad R, Amigo José M, Rantanen Jukka, Poppi Ronei J

机构信息

Institute of Chemistry, State University of Campinas - UNICAMP, P.O. Box 6154, 13084-971 Campinas, SP, Brazil.

Department of Pharmaceutics and Analytical Chemistry, Faculty of Pharmaceutical Sciences, University of Copenhagen, Universitetsparken 2, 2100 Copenhagen, Denmark.

出版信息

Eur J Pharm Biopharm. 2015 Jun;93:224-30. doi: 10.1016/j.ejpb.2015.03.034. Epub 2015 Apr 20.

Abstract

The assessment of the solid-state stability of active pharmaceutical ingredient (API) and/or excipients in solid dosage forms during manufacturing and storage is mandatory for safeguarding quality of the final products. In this work, the solid-state transformations in tablets prepared as blends of piroxicam monohydrate, polyvinylpyrrolidone and the lactose forms monohydrate or anhydrate were studied when the tablets were exposed to the 23-120 °C range. Multi-series near-infrared hyperspectral images were obtained from the surface of each sample for unveiling the local evolution of the solid-state transformations. The preprocessed spectra from the images (dataset) were arranged in augmented matrices, according to the composition of the tablets, and the profile of the overlapped compounds (relative concentration) along the solid-state transformations in the pixels was resolved by using multivariate curve resolution--alternating least squares (MCR-ALS). Therefore, the dehydration of piroxicam and lactose monohydrates could be mapped separately in the samples (explained variances by the models >96%) even when both compounds were being transformed simultaneously (80-120 °C). The images reproduced the same trends obtained from thermogravimetric analysis of the tablets, with the advantage that the pixel-to-pixel heterogeneity of each compound at the surface of the tablets was highlighted.

摘要

在制造和储存过程中评估固体剂型中活性药物成分(API)和/或辅料的固态稳定性对于保障最终产品质量至关重要。在这项工作中,研究了将吡罗昔康一水合物、聚乙烯吡咯烷酮与一水合物或无水合物形式的乳糖混合制备的片剂在23至120°C范围内暴露时的固态转变。从每个样品表面获取多系列近红外高光谱图像,以揭示固态转变的局部演变。根据片剂的组成,将图像(数据集)的预处理光谱排列在增强矩阵中,并使用多元曲线分辨-交替最小二乘法(MCR-ALS)解析像素中沿固态转变的重叠化合物(相对浓度)的分布。因此,即使两种化合物同时发生转变(80至120°C),吡罗昔康和乳糖一水合物的脱水也可以在样品中分别绘制出来(模型解释方差>96%)。这些图像再现了从片剂热重分析获得的相同趋势,其优点是突出了片剂表面每种化合物的逐像素异质性。

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