Boiret Mathieu, Rutledge Douglas N, Gorretta Nathalie, Ginot Yves-Michel, Roger Jean-Michel
Technologie Servier, 27 rue Eugène Vignat, 45000 Orléans, France.
AgroParisTech, UMR 1145 Ingénierie Procédés Aliments, rue Claude Bernard, F-75005 Paris, France.
J Pharm Biomed Anal. 2014 Mar;90:78-84. doi: 10.1016/j.jpba.2013.11.025. Epub 2013 Dec 1.
Independent component analysis (ICA) was used as a blind source separation method on a Raman image of a pharmaceutical tablet. Calculations were performed without a priori knowledge concerning the formulation. The aim was to extract the pure signals from the initial data set in order to examine the distribution of actives and major excipients within the tablet. As a method based on the decomposition of a matrix of mixtures of several components, the number of independent component to choose is a critical step of the analysis. The ICA_by_blocks method, based on the calculation of several models using an increasing number of independent components on initial matrix blocks, was used. The calculated ICA signals were compared with the pure spectra of the formulation compounds. High correlations between the two active principal ingredient spectra and their corresponding calculated signals were observed giving a good overview of the distributions of these compounds within the tablet. Information from the major excipients (lactose and avicel) was found in several independent components but the ICA approach provides high level of information concerning their distribution within the tablet. However, the results could vary considerably by changing the number of independent components or the preprocessing method. Indeed, it was shown that under-decomposition of the matrix could lead to better signal quality (compared to the pure spectra) but in that case the contributions due to minor components or effects were not correctly identified and extracted. On the contrary, over-decomposition of the original dataset could provide information about low concentration compounds at the expense of some loss of signal interpretability for the other compounds.
独立成分分析(ICA)被用作一种盲源分离方法,用于分析一片药的拉曼图像。计算过程中无需关于配方的先验知识。目的是从初始数据集中提取纯信号,以便研究片剂中活性成分和主要辅料的分布情况。作为一种基于对几种成分混合物矩阵进行分解的方法,选择独立成分的数量是分析的关键步骤。使用了ICA_by_blocks方法,该方法基于对初始矩阵块使用越来越多的独立成分来计算多个模型。将计算得到的ICA信号与配方化合物的纯光谱进行比较。观察到两种活性主要成分光谱与其相应计算信号之间具有高度相关性,从而很好地了解了这些化合物在片剂中的分布情况。在几个独立成分中发现了来自主要辅料(乳糖和微晶纤维素)的信息,但ICA方法提供了有关它们在片剂中分布的高水平信息。然而,通过改变独立成分的数量或预处理方法,结果可能会有很大差异。事实上,结果表明,矩阵分解不足可能会导致更好的信号质量(与纯光谱相比),但在这种情况下,微量成分或效应的贡献无法正确识别和提取。相反,对原始数据集进行过度分解可能会以牺牲其他化合物的一些信号可解释性为代价,提供有关低浓度化合物的信息。