Cited by 86Spectroscopy and Chemometric AnalysesSpectroscopy Techniques in Biomedical and Chemical ResearchAnalytical Methods in Pharmaceuticals

Process analytical technology: chemometric analysis of Raman and near infra-red spectroscopic data for predicting physical properties of extended release matrix tablets

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Shah, Rakhi B., Tawakkul, Mobin A., Khan, Mansoor A.·2007·Journal of Pharmaceutical Sciences

Abstract

The purpose of this work was to develop a correlation between pharmaceutical properties such as hardness, porosity, and content with prediction models employed using Raman and near infra-red (NIR) spectroscopic methods. Metoprolol tartrate tablets were prepared by direct compression and wet granulation methods. NIR spectroscopy and chemical imaging, and Raman spectra were collected, and hardness, porosity, and dissolution were measured. The NIR PLS model showed a validated correlation coefficient of >0.90 for the predicted versus measured porosity, hardness, and amount of drug with raw and second derivative NIR spectra. Raman spectra correlated porosity of the tablets using raw data for directly compressed tablets and wet granulated tablets (r(2) > 0.90). A very close root-mean square error of calibration (RMSEC) and root-mean square error of prediction (RMSEP) values were found in all the cases indicating validity of the calibration models. Raman spectroscopy was used for the first time to predict physical quality attribute such as porosity successfully. Chemical imaging utilizing NIR detector also demonstrated to show physical changes due to compression differences. In conclusion, sensor technologies can be potentially used to predict physical parameters of the matrix tablets.

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  • NIR and Raman porosity predictions are surface-sensitive and model-dependent, so they may not represent the tablet's bulk.

    “Yet, these methods typically only probe surface properties and rely on the use of chemometric models.Given the surface measurement, the results may not necessarily represent the bulk tablet property.”

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References 23 · Cited by 86

Authors
Shah, R. B., Tawakkul, M. A., & Khan, M. A.
Affiliations
United States Food and Drug Administration (US)
Corresponding author
Khan, Mansoor A.
Venue
Journal of Pharmaceutical Sciences
Publisher
Elsevier BV
Published
2007-05
Volume
96
Issue
5
Pages
1356-1365
ISSN
0022-3549 (ISSN-L)
OpenAlex
W2073373037
Cited by
86
References
23
Citations by year
2026: 2 · 2025: 5 · 2024: 5 · 2023: 2 · 2022: 1 · 2021: 2 · 2020: 4 · 2019: 2 · 2018: 2 · 2017: 2 · 2016: 5 · 2015: 9 · 2014: 2 · 2013: 6 · 2012: 6
FWCI
8.82
Type
journal article
Language
en
Open access
Locations
  • Journal of Pharmaceutical Sciences (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Physical Sciences › Chemistry › Analytical Chemistry › Spectroscopy and Chemometric Analyses
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Biophysics › Spectroscopy Techniques in Biomedical and Chemical Research
  • Physical Sciences › Chemistry › Analytical Chemistry › Analytical Methods in Pharmaceuticals
Keywords
process analytical technology, metoprolol tartrate, Raman spectroscopy, near-infrared spectroscopy, chemical imaging, porosity estimation, tablet hardness, dissolution prediction, direct compression, wet granulation, second derivative spectra
MeSH terms
Adrenergic beta-Antagonists, Calibration, Chemistry, Pharmaceutical, Delayed-Action Preparations, Drug Carriers, Drug Compounding, Hardness, Methacrylates, Metoprolol, Models, Chemical, Predictive Value of Tests, Quality Control, Solubility, Spectrum Analysis, Raman, Tablets, Technology, Pharmaceutical, Time Factors, Reproducibility of Results, Least-Squares Analysis, Porosity, Spectroscopy, Near-Infrared

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