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Fluorescence Spectrometric Determination of Drugs Containing α-Methylene Sulfone/Sulfonamide Functional Groups Using N (1)-Methylnicotinamide Chloride as a Fluorogenic Agent
A simple spectrofluorometric method has been developed, adapted, and validated for the quantitative estimation of drugs containing α-methylene sulfone/sulfonamide functional groups using N (1)-methylnicotinamide chloride (NMNCl) as fluorogenic agent. The proposed method has been applied successfully...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103861/ https://www.ncbi.nlm.nih.gov/pubmed/21647288 http://dx.doi.org/10.1155/2011/840178 |
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author | Elokely, Khaled M. Eldawy, Mohamed A. Elkersh, Mohamed A. El-Moselhy, Tarek F. |
author_facet | Elokely, Khaled M. Eldawy, Mohamed A. Elkersh, Mohamed A. El-Moselhy, Tarek F. |
author_sort | Elokely, Khaled M. |
collection | PubMed |
description | A simple spectrofluorometric method has been developed, adapted, and validated for the quantitative estimation of drugs containing α-methylene sulfone/sulfonamide functional groups using N (1)-methylnicotinamide chloride (NMNCl) as fluorogenic agent. The proposed method has been applied successfully to the determination of methyl sulfonyl methane (MSM) (1), tinidazole (2), rofecoxib (3), and nimesulide (4) in pure forms, laboratory-prepared mixtures, pharmaceutical dosage forms, spiked human plasma samples, and in volunteer's blood. The method showed linearity over concentration ranging from 1 to 150 μg/mL, 10 to 1000 ng/mL, 1 to 1800 ng/mL, and 30 to 2100 ng/mL for standard solutions of 1, 2, 3, and 4, respectively, and over concentration ranging from 5 to 150 μg/mL, 10 to 1000 ng/mL, 10 to 1700 ng/mL, and 30 to 2350 ng/mL in spiked human plasma samples of 1, 2, 3, and 4, respectively. The method showed good accuracy, specificity, and precision in both laboratory-prepared mixtures and in spiked human plasma samples. The proposed method is simple, does not need sophisticated instruments, and is suitable for quality control application, bioavailability, and bioequivalency studies. Besides, its detection limits are comparable to other sophisticated chromatographic methods. |
format | Text |
id | pubmed-3103861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-31038612011-06-06 Fluorescence Spectrometric Determination of Drugs Containing α-Methylene Sulfone/Sulfonamide Functional Groups Using N (1)-Methylnicotinamide Chloride as a Fluorogenic Agent Elokely, Khaled M. Eldawy, Mohamed A. Elkersh, Mohamed A. El-Moselhy, Tarek F. Int J Anal Chem Research Article A simple spectrofluorometric method has been developed, adapted, and validated for the quantitative estimation of drugs containing α-methylene sulfone/sulfonamide functional groups using N (1)-methylnicotinamide chloride (NMNCl) as fluorogenic agent. The proposed method has been applied successfully to the determination of methyl sulfonyl methane (MSM) (1), tinidazole (2), rofecoxib (3), and nimesulide (4) in pure forms, laboratory-prepared mixtures, pharmaceutical dosage forms, spiked human plasma samples, and in volunteer's blood. The method showed linearity over concentration ranging from 1 to 150 μg/mL, 10 to 1000 ng/mL, 1 to 1800 ng/mL, and 30 to 2100 ng/mL for standard solutions of 1, 2, 3, and 4, respectively, and over concentration ranging from 5 to 150 μg/mL, 10 to 1000 ng/mL, 10 to 1700 ng/mL, and 30 to 2350 ng/mL in spiked human plasma samples of 1, 2, 3, and 4, respectively. The method showed good accuracy, specificity, and precision in both laboratory-prepared mixtures and in spiked human plasma samples. The proposed method is simple, does not need sophisticated instruments, and is suitable for quality control application, bioavailability, and bioequivalency studies. Besides, its detection limits are comparable to other sophisticated chromatographic methods. Hindawi Publishing Corporation 2011 2011-05-16 /pmc/articles/PMC3103861/ /pubmed/21647288 http://dx.doi.org/10.1155/2011/840178 Text en Copyright © 2011 Khaled M. Elokely et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Elokely, Khaled M. Eldawy, Mohamed A. Elkersh, Mohamed A. El-Moselhy, Tarek F. Fluorescence Spectrometric Determination of Drugs Containing α-Methylene Sulfone/Sulfonamide Functional Groups Using N (1)-Methylnicotinamide Chloride as a Fluorogenic Agent |
title | Fluorescence Spectrometric Determination of Drugs Containing α-Methylene Sulfone/Sulfonamide Functional Groups Using N
(1)-Methylnicotinamide Chloride as a Fluorogenic Agent |
title_full | Fluorescence Spectrometric Determination of Drugs Containing α-Methylene Sulfone/Sulfonamide Functional Groups Using N
(1)-Methylnicotinamide Chloride as a Fluorogenic Agent |
title_fullStr | Fluorescence Spectrometric Determination of Drugs Containing α-Methylene Sulfone/Sulfonamide Functional Groups Using N
(1)-Methylnicotinamide Chloride as a Fluorogenic Agent |
title_full_unstemmed | Fluorescence Spectrometric Determination of Drugs Containing α-Methylene Sulfone/Sulfonamide Functional Groups Using N
(1)-Methylnicotinamide Chloride as a Fluorogenic Agent |
title_short | Fluorescence Spectrometric Determination of Drugs Containing α-Methylene Sulfone/Sulfonamide Functional Groups Using N
(1)-Methylnicotinamide Chloride as a Fluorogenic Agent |
title_sort | fluorescence spectrometric determination of drugs containing α-methylene sulfone/sulfonamide functional groups using n
(1)-methylnicotinamide chloride as a fluorogenic agent |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103861/ https://www.ncbi.nlm.nih.gov/pubmed/21647288 http://dx.doi.org/10.1155/2011/840178 |
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