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Spectrofluorimetric Method for Determination of Citalopram in Bulk and Pharmaceutical Dosage Forms
A simple accurate, sensitive reproducible spectrofluorimetric method was developed for the analysis of citalopram in pure and pharmaceutical dosage form. Citalopram showed strong native fluorescence in 0.05 M sulphuric acid having excitation at 239 nm and emission at 300 nm. All parameters like the...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Medknow Publications
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038293/ https://www.ncbi.nlm.nih.gov/pubmed/21394265 http://dx.doi.org/10.4103/0250-474X.45407 |
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author | Vasantharaju, S. G. Prabu, S. Lakshmana Jacob, A. |
author_facet | Vasantharaju, S. G. Prabu, S. Lakshmana Jacob, A. |
author_sort | Vasantharaju, S. G. |
collection | PubMed |
description | A simple accurate, sensitive reproducible spectrofluorimetric method was developed for the analysis of citalopram in pure and pharmaceutical dosage form. Citalopram showed strong native fluorescence in 0.05 M sulphuric acid having excitation at 239 nm and emission at 300 nm. All parameters like the effect of different solvents, pH, dilutions, reaction time, temperature and effect of excipients were thoroughly investigated. The calibration graph was linear in the range from 0.100 to 0.900 μg/ml. The proposed method was statistically validated and successfully applied for analysis of tablet dosage forms. The percentage recovery was found to be between 99.08% to 99.28%. |
format | Text |
id | pubmed-3038293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-30382932011-03-10 Spectrofluorimetric Method for Determination of Citalopram in Bulk and Pharmaceutical Dosage Forms Vasantharaju, S. G. Prabu, S. Lakshmana Jacob, A. Indian J Pharm Sci Short Communication A simple accurate, sensitive reproducible spectrofluorimetric method was developed for the analysis of citalopram in pure and pharmaceutical dosage form. Citalopram showed strong native fluorescence in 0.05 M sulphuric acid having excitation at 239 nm and emission at 300 nm. All parameters like the effect of different solvents, pH, dilutions, reaction time, temperature and effect of excipients were thoroughly investigated. The calibration graph was linear in the range from 0.100 to 0.900 μg/ml. The proposed method was statistically validated and successfully applied for analysis of tablet dosage forms. The percentage recovery was found to be between 99.08% to 99.28%. Medknow Publications 2008 /pmc/articles/PMC3038293/ /pubmed/21394265 http://dx.doi.org/10.4103/0250-474X.45407 Text en © Indian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Vasantharaju, S. G. Prabu, S. Lakshmana Jacob, A. Spectrofluorimetric Method for Determination of Citalopram in Bulk and Pharmaceutical Dosage Forms |
title | Spectrofluorimetric Method for Determination of Citalopram in Bulk and Pharmaceutical Dosage Forms |
title_full | Spectrofluorimetric Method for Determination of Citalopram in Bulk and Pharmaceutical Dosage Forms |
title_fullStr | Spectrofluorimetric Method for Determination of Citalopram in Bulk and Pharmaceutical Dosage Forms |
title_full_unstemmed | Spectrofluorimetric Method for Determination of Citalopram in Bulk and Pharmaceutical Dosage Forms |
title_short | Spectrofluorimetric Method for Determination of Citalopram in Bulk and Pharmaceutical Dosage Forms |
title_sort | spectrofluorimetric method for determination of citalopram in bulk and pharmaceutical dosage forms |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038293/ https://www.ncbi.nlm.nih.gov/pubmed/21394265 http://dx.doi.org/10.4103/0250-474X.45407 |
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