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Authentication of Antibiotics Using Portable Near-Infrared Spectroscopy and Multivariate Data Analysis
Counterfeit medicines represent a global public health threat warranting the development of accurate, rapid, and nondestructive methods for their identification. Portable near-infrared (NIR) spectroscopy offers this advantage. This work sheds light on the potential of combining NIR spectroscopy with...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645310/ https://www.ncbi.nlm.nih.gov/pubmed/32830991 http://dx.doi.org/10.1177/0003702820958081 |
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author | Assi, Sulaf Arafat, Basel Lawson-Wood, Kathryn Robertson, Ian |
author_facet | Assi, Sulaf Arafat, Basel Lawson-Wood, Kathryn Robertson, Ian |
author_sort | Assi, Sulaf |
collection | PubMed |
description | Counterfeit medicines represent a global public health threat warranting the development of accurate, rapid, and nondestructive methods for their identification. Portable near-infrared (NIR) spectroscopy offers this advantage. This work sheds light on the potential of combining NIR spectroscopy with principal component analysis (PCA) and soft independent modelling of class analogy (SIMCA) for authenticating branded and generic antibiotics. A total of 23 antibiotics were measured “nondestructively” using a portable NIR spectrometer. The antibiotics corresponded to six different active pharmaceutical ingredients being: amoxicillin trihydrate and clavulanic acid, azithromycin dihydrate, ciprofloxacin hydrochloride, doxycycline hydrochloride, and ofloxacin. NIR spectra were exported into Matlab R2018b where data analysis was applied. The results showed that the NIR spectra of the medicines showed characteristic features that corresponded to the main excipient(s). When combined with PCA, NIR spectroscopy could distinguish between branded and generic medicines and could classify medicines according to their manufacturing sources. The PCA scores showed the distinct clusters corresponding to each group of antibiotics, whereas the loadings indicated which spectral features were significant. SIMCA provided more accurate classification over PCA for all antibiotics except ciprofloxacin which products shared many overlapping excipients. In summary, the findings of the study demonstrated the feasibility of portable NIR as an initial method for screening antibiotics. |
format | Online Article Text |
id | pubmed-8645310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-86453102021-12-06 Authentication of Antibiotics Using Portable Near-Infrared Spectroscopy and Multivariate Data Analysis Assi, Sulaf Arafat, Basel Lawson-Wood, Kathryn Robertson, Ian Appl Spectrosc Articles Counterfeit medicines represent a global public health threat warranting the development of accurate, rapid, and nondestructive methods for their identification. Portable near-infrared (NIR) spectroscopy offers this advantage. This work sheds light on the potential of combining NIR spectroscopy with principal component analysis (PCA) and soft independent modelling of class analogy (SIMCA) for authenticating branded and generic antibiotics. A total of 23 antibiotics were measured “nondestructively” using a portable NIR spectrometer. The antibiotics corresponded to six different active pharmaceutical ingredients being: amoxicillin trihydrate and clavulanic acid, azithromycin dihydrate, ciprofloxacin hydrochloride, doxycycline hydrochloride, and ofloxacin. NIR spectra were exported into Matlab R2018b where data analysis was applied. The results showed that the NIR spectra of the medicines showed characteristic features that corresponded to the main excipient(s). When combined with PCA, NIR spectroscopy could distinguish between branded and generic medicines and could classify medicines according to their manufacturing sources. The PCA scores showed the distinct clusters corresponding to each group of antibiotics, whereas the loadings indicated which spectral features were significant. SIMCA provided more accurate classification over PCA for all antibiotics except ciprofloxacin which products shared many overlapping excipients. In summary, the findings of the study demonstrated the feasibility of portable NIR as an initial method for screening antibiotics. SAGE Publications 2020-10-14 2021-04 /pmc/articles/PMC8645310/ /pubmed/32830991 http://dx.doi.org/10.1177/0003702820958081 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Articles Assi, Sulaf Arafat, Basel Lawson-Wood, Kathryn Robertson, Ian Authentication of Antibiotics Using Portable Near-Infrared Spectroscopy and Multivariate Data Analysis |
title | Authentication of Antibiotics Using Portable Near-Infrared
Spectroscopy and Multivariate Data Analysis |
title_full | Authentication of Antibiotics Using Portable Near-Infrared
Spectroscopy and Multivariate Data Analysis |
title_fullStr | Authentication of Antibiotics Using Portable Near-Infrared
Spectroscopy and Multivariate Data Analysis |
title_full_unstemmed | Authentication of Antibiotics Using Portable Near-Infrared
Spectroscopy and Multivariate Data Analysis |
title_short | Authentication of Antibiotics Using Portable Near-Infrared
Spectroscopy and Multivariate Data Analysis |
title_sort | authentication of antibiotics using portable near-infrared
spectroscopy and multivariate data analysis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645310/ https://www.ncbi.nlm.nih.gov/pubmed/32830991 http://dx.doi.org/10.1177/0003702820958081 |
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