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Variable clustering and spectral angle mapper-orthogonal projection method for Raman mapping of compound detection in tablets

机译:平板电脑复合检测拉曼映射的可变聚类和光谱角映射 - 正交投影

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Raman mapping and chemometrics are proposed to accurately characterize the composition of tablets. The most critical step of the state-of-art curve resolution methods (such as multivariate curve resolution-alternating least squares [MCR-ALS]) is the determination of the number of constituents, when chemical imaging is coupled with multivariate data analysis. However, it is usually performed in a considerably subjective way. We propose a variable clustering approach for the identification of the main dimensionality of vibrational spectral data. The method was tested on a Raman map of a complex pharmaceutical tablet that contained 4 major components with high spectral resemblance, and a low-dose lubricant was also added for tableting purposes. Using a variable clustering algorithm called VARCLUS we were able to construct clusters from the Raman mapping data corresponding to the real constitution of the sample. The modeled clusters were analyzed by the sum of ranking differences method. All 4 major components could be identified. The potential of the clustering algorithm was further assessed by applying MCR-ALS and spectral angle mapper-orthogonal projection methods. We have shown that variable clustering corresponded with MCR-ALS results and that it can be used to characterize the qualitative composition of an unknown pharmaceutical sample by combining the clustering algorithm with a pure component resolution method. Therefore, this method is well applicable to analyze and interpret the curve resolution of complex samples. Testing of the previously studied spectral angle mapper-orthogonal projection method, which relies on spectral reference libraries and even the low-dose lubricant (approximately 1% w/w), was identified through the chemical imaging.
机译:拉曼图谱和化学计量学被用来准确描述片剂的组成。当化学成像与多元数据分析相结合时,最先进的曲线分辨率方法(如多元曲线分辨率交替最小二乘法[MCR-ALS])最关键的一步是确定成分的数量。然而,它通常是以相当主观的方式执行的。我们提出了一种用于识别振动光谱数据主要维度的变量聚类方法。该方法在一种复杂药物片剂的拉曼图谱上进行了测试,该片剂含有4种主要成分,光谱相似性很高,并且还添加了一种低剂量润滑剂用于压片。使用变量聚类算法VARCLUS,我们能够从拉曼映射数据中构造出与样本真实成分相对应的聚类。模型聚类采用排序差异总和法进行分析。所有4个主要组件都可以识别。通过应用MCR-ALS和光谱角度映射正交投影方法,进一步评估了聚类算法的潜力。我们已经证明,变量聚类与MCR-ALS结果一致,并且通过将聚类算法与纯组分解析方法相结合,它可以用来表征未知药物样品的定性成分。因此,该方法适用于分析和解释复杂样品的曲线分辨率。通过化学成像,对之前研究的光谱角度映射器正交投影法进行了测试,该方法依赖于光谱参考库,甚至是低剂量润滑剂(约1%w/w)。

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