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Issue 44, 2017
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Chemometric approaches to low-content quantification (LCQ) in solid-state mixtures using Raman mapping spectroscopy

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Abstract

The low-content quantification (LCQ) of active pharmaceutical ingredients or impurities in solid mixtures is important in pharmaceutical manufacturing and analysis. We previously demonstrated the feasibility of using Raman mapping of the micro-scale heterogeneity in solid-state samples combined with partial least squares (PLS) regression for LCQ in a binary system. However, PLS is limited by the need for relatively large calibration sample numbers to attain high accuracy, and a rather significant computational time requirement for processing large Raman maps. Here we evaluated alternative chemometric methods which might overcome these issues. The methods were: net analyte signal coupled with classical least squares (NAS-CLS), multivariate curve resolution (MCR), principal component analysis with CLS (PCA-CLS), and the ratio of characteristic analyte/matrix bands combined with shape-preserving piecewise cubic polynomial interpolation curve fitting (BR-PCHIP). For high (>1.0%) piracetam analyte content, all methods were accurate with relative errors of prediction (REP) of <1.1%. For LCQ (0.05–1.0% w/w), three methods were able to predict piracetam content with reasonable levels of accuracy: 6.97% (PCA-CLS), 9.13% (MCR), and 12.8% (NAS-CLS). MCR offered the best potential as a semi-quantitative screening method as it was ∼40% quicker than PLS, but was less accurate due to being more sensitive to spectral noise factors.

Graphical abstract: Chemometric approaches to low-content quantification (LCQ) in solid-state mixtures using Raman mapping spectroscopy

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Publication details

The article was received on 21 Jul 2017, accepted on 28 Oct 2017 and first published on 30 Oct 2017


Article type: Paper
DOI: 10.1039/C7AY01778B
Citation: Anal. Methods, 2017,9, 6293-6301
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    Chemometric approaches to low-content quantification (LCQ) in solid-state mixtures using Raman mapping spectroscopy

    B. Li, Y. Casamayou-Boucau, A. Calvet and A. G. Ryder, Anal. Methods, 2017, 9, 6293
    DOI: 10.1039/C7AY01778B

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