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J Pharm Biomed Anal ; 151: 186-193, 2018 Mar 20.
Article in English | MEDLINE | ID: mdl-29353807

ABSTRACT

A system using energy-dispersive X-ray diffraction (EDXRD) has been developed and tested using multivariate calibration for the quantitative analysis of tablet-form mixtures of common pharmaceutical ingredients. A principal advantage of EDXRD over the more traditional and common angular dispersive X-ray diffraction technique (ADXRD) is the potential of EDXRD to analyse tablets within their packaging, due to the higher energy X-rays used. In the experiment, a series of caffeine, paracetamol and microcrystalline cellulose mixtures were prepared and pressed into tablets. EDXRD profiles were recorded on each sample and a principal component analysis (PCA) was carried out in both unpackaged and packaged scenarios. In both cases the first two principal components explained >98% of the between-sample variance. The PCA projected the sample profiles into two dimensional principal component space in close accordance to their ternary mixture design, demonstrating the discriminating potential of the EDXRD system. A partial least squares regression (PLSR) model was built with the samples and was validated using leave-one-out cross-validation. Low prediction errors of between 2% and 4% for both unpackaged and packaged tablets were obtained for all three chemical compounds. The prediction capability through packaging demonstrates a truly non-destructive method for quantifying tablet composition and demonstrates good potential for EDXRD to be applied in the field of counterfeit medicine screening and pharmaceutical quality control.


Subject(s)
Counterfeit Drugs/analysis , Quality Control , Tablets/analysis , X-Ray Diffraction/methods , Calibration , Chemistry, Pharmaceutical/instrumentation , Chemistry, Pharmaceutical/methods , Chemistry, Pharmaceutical/organization & administration , Drug Packaging , Least-Squares Analysis , Principal Component Analysis , X-Ray Diffraction/instrumentation
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