Process analytical technology: chemometric analysis of Raman and near infra-red spectroscopic data for predicting physical properties of extended release matrix tablets
Open accessAbstract
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.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
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.”
From A Fast and Non-destructive Terahertz Dissolution Assay for Immediate Release Tablets (2021) · cites this paper as [7]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
The citation lists haven’t been fetched yet
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.
- ORCID
- 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
- bronze
- doi.org
- 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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review