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Validated stability indicating methods for determination of nitazoxanide in presence of its degradation products()
Three sensitive, selective and reproducible stability-indicating methods are presented for determination of nitazoxanide (NTZ), a new anti-protozoal drug, in presence of its degradation products. Method A utilizes the first derivative of ratio spectra spectrophotometry by measurement of the amplitud...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Xi'an Jiaotong University
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760833/ https://www.ncbi.nlm.nih.gov/pubmed/29403729 http://dx.doi.org/10.1016/j.jpha.2011.11.004 |
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author | Ali, Nouruddin W. Abbas, Samah Sayed Zaazaa, Hala El-Sayed Abdelrahman, Maha Mohamed Abdelkawy, Mohamed |
author_facet | Ali, Nouruddin W. Abbas, Samah Sayed Zaazaa, Hala El-Sayed Abdelrahman, Maha Mohamed Abdelkawy, Mohamed |
author_sort | Ali, Nouruddin W. |
collection | PubMed |
description | Three sensitive, selective and reproducible stability-indicating methods are presented for determination of nitazoxanide (NTZ), a new anti-protozoal drug, in presence of its degradation products. Method A utilizes the first derivative of ratio spectra spectrophotometry by measurement of the amplitude at 364.4 nm using one of the degradation products as a divisor. Method B is a chemometric-assisted spectrophotometry, where principal component regression (PCR) and partial least squares (PLS) were applied. These two approaches were successfully applied to quantify NTZ in presence of degradation products using the information included in the absorption spectra in the range 260–360 nm. Method C is based on the separation of NTZ from its degradation products followed by densitometric measurement of the bands at 254 nm. The separation was carried out on silica gel 60F(254), using chloroform–methanol–ammonia solution–glacial acetic acid (95:5:1:1 by volume, pH=5.80) as a developing system. These methods are suitable as stability-indicating methods for the determination of NTZ in presence of its degradation products either in bulk powder or in pharmaceutical formulations. Statistical analysis of the results has been carried out revealing high accuracy and good precision. |
format | Online Article Text |
id | pubmed-5760833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Xi'an Jiaotong University |
record_format | MEDLINE/PubMed |
spelling | pubmed-57608332018-02-05 Validated stability indicating methods for determination of nitazoxanide in presence of its degradation products() Ali, Nouruddin W. Abbas, Samah Sayed Zaazaa, Hala El-Sayed Abdelrahman, Maha Mohamed Abdelkawy, Mohamed J Pharm Anal Article Three sensitive, selective and reproducible stability-indicating methods are presented for determination of nitazoxanide (NTZ), a new anti-protozoal drug, in presence of its degradation products. Method A utilizes the first derivative of ratio spectra spectrophotometry by measurement of the amplitude at 364.4 nm using one of the degradation products as a divisor. Method B is a chemometric-assisted spectrophotometry, where principal component regression (PCR) and partial least squares (PLS) were applied. These two approaches were successfully applied to quantify NTZ in presence of degradation products using the information included in the absorption spectra in the range 260–360 nm. Method C is based on the separation of NTZ from its degradation products followed by densitometric measurement of the bands at 254 nm. The separation was carried out on silica gel 60F(254), using chloroform–methanol–ammonia solution–glacial acetic acid (95:5:1:1 by volume, pH=5.80) as a developing system. These methods are suitable as stability-indicating methods for the determination of NTZ in presence of its degradation products either in bulk powder or in pharmaceutical formulations. Statistical analysis of the results has been carried out revealing high accuracy and good precision. Xi'an Jiaotong University 2012-04 2011-11-30 /pmc/articles/PMC5760833/ /pubmed/29403729 http://dx.doi.org/10.1016/j.jpha.2011.11.004 Text en © 2012 Xi'an Jiaotong University http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Article Ali, Nouruddin W. Abbas, Samah Sayed Zaazaa, Hala El-Sayed Abdelrahman, Maha Mohamed Abdelkawy, Mohamed Validated stability indicating methods for determination of nitazoxanide in presence of its degradation products() |
title | Validated stability indicating methods for determination of nitazoxanide in presence of its degradation products() |
title_full | Validated stability indicating methods for determination of nitazoxanide in presence of its degradation products() |
title_fullStr | Validated stability indicating methods for determination of nitazoxanide in presence of its degradation products() |
title_full_unstemmed | Validated stability indicating methods for determination of nitazoxanide in presence of its degradation products() |
title_short | Validated stability indicating methods for determination of nitazoxanide in presence of its degradation products() |
title_sort | validated stability indicating methods for determination of nitazoxanide in presence of its degradation products() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760833/ https://www.ncbi.nlm.nih.gov/pubmed/29403729 http://dx.doi.org/10.1016/j.jpha.2011.11.004 |
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