Quantification of paracetamol in intact tablets using near-infrared transmittance spectroscopy

Authors:
  • PGPaul Graham
    Paul Graham
  • RJRoger D. Jee
    Roger D. Jee
  • AMAnthony C. Moffatt
    Anthony C. Moffatt
  • ATAndrew D. Trafford
    Andrew D. Trafford
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Abstract
Production batch samples of paracetamol tablets and specially prepared out-of-specification batches covering the range 90–110% of the stated amount (500 mg) were analysed by the BP official UV assay and by NIR transmittance spectroscopy. NIR measurements were made on 20 intact tablets from each batch, scanned five times each (10 min measurement time per batch) over the spectral range 6000–11520 cm– 1. An average spectrum was calculated for each batch. Partial least squares (PLS) regression models were set up using a calibration set (20 batches) between the NIR response and the reference tablet paracetamol content (UV). Various pre-treatments of the spectra were examined; the smallest relative standard error of prediction (0.73%) was obtained using the first derivative of the absorbance over the full spectrum. Only two principal components were required for the PLS model to give a good relationship between the spectral information and paracetamol content. Applying this model to the validation set (15 batches) gave a mean bias of –0.08% and a mean accuracy of 0.59% with relative standard deviations of 0.75 and 0.44%, respectively. The proposed method is non-destructive and therefore lends itself to on-line/at-line production control purposes. The method is easy to use and does not require a knowledge of the mass of the tablets.