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Sensitive Indirect Spectrophotometric Method for Determination of H(2)-Receptor Antagonists in Pharmaceutical Formulations
A simple, accurate and sensitive spectrophotometric method has been developed and validated for determination of H(2)-receptor antagonists: cimetidine, famotidine, nizatidine, and ranitidine hydrochloride. The method was based on the oxidation of these drugs with cerium (IV) in presence of perchlori...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Master Publishing Group
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3614635/ https://www.ncbi.nlm.nih.gov/pubmed/23675034 |
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author | Darwish, Ibrahim A. Hussein, Samiha A. Mahmoud, Ashraf M. Hassan, Ahmed I. |
author_facet | Darwish, Ibrahim A. Hussein, Samiha A. Mahmoud, Ashraf M. Hassan, Ahmed I. |
author_sort | Darwish, Ibrahim A. |
collection | PubMed |
description | A simple, accurate and sensitive spectrophotometric method has been developed and validated for determination of H(2)-receptor antagonists: cimetidine, famotidine, nizatidine, and ranitidine hydrochloride. The method was based on the oxidation of these drugs with cerium (IV) in presence of perchloric acid and subsequent measurement of the excess Ce (IV) by its reaction with p-dimethylaminocinnamaldehyde to give a red colored product (λ(max) at 464 nm). The decrease in the absorption intensity (ΔA) of the colored product, due to the presence of the drug was correlated with its concentration in the sample solution. Different variables affecting the reaction were carefully studied and optimized. Under the optimum conditions, linear relationships with good correlation coefficients (0.9985-0.9994) were found between ΔA values and the concentrations of the drugs in a concentration range of 1-16 µg ml(-1). The assay limits of detection and quantitation were 0.12-0.44 and 0.37-1.33 µg ml(-1), respectively. The method was validated, in terms of accuracy, precision, ruggedness, and robustness; the results were satisfactory. The proposed method was successfully applied to the analysis of the investigated drugs in their pure and pharmaceutical dosage forms (recovery was 98.8-102.5 ± 0.79-1.72%) without interference from the common excipients. The results obtained by the proposed method were comparable with those obtained by the official methods. |
format | Online Article Text |
id | pubmed-3614635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Master Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-36146352013-05-01 Sensitive Indirect Spectrophotometric Method for Determination of H(2)-Receptor Antagonists in Pharmaceutical Formulations Darwish, Ibrahim A. Hussein, Samiha A. Mahmoud, Ashraf M. Hassan, Ahmed I. Int J Biomed Sci Article A simple, accurate and sensitive spectrophotometric method has been developed and validated for determination of H(2)-receptor antagonists: cimetidine, famotidine, nizatidine, and ranitidine hydrochloride. The method was based on the oxidation of these drugs with cerium (IV) in presence of perchloric acid and subsequent measurement of the excess Ce (IV) by its reaction with p-dimethylaminocinnamaldehyde to give a red colored product (λ(max) at 464 nm). The decrease in the absorption intensity (ΔA) of the colored product, due to the presence of the drug was correlated with its concentration in the sample solution. Different variables affecting the reaction were carefully studied and optimized. Under the optimum conditions, linear relationships with good correlation coefficients (0.9985-0.9994) were found between ΔA values and the concentrations of the drugs in a concentration range of 1-16 µg ml(-1). The assay limits of detection and quantitation were 0.12-0.44 and 0.37-1.33 µg ml(-1), respectively. The method was validated, in terms of accuracy, precision, ruggedness, and robustness; the results were satisfactory. The proposed method was successfully applied to the analysis of the investigated drugs in their pure and pharmaceutical dosage forms (recovery was 98.8-102.5 ± 0.79-1.72%) without interference from the common excipients. The results obtained by the proposed method were comparable with those obtained by the official methods. Master Publishing Group 2007-06 /pmc/articles/PMC3614635/ /pubmed/23675034 Text en © Ibrahim A. Darwish et al. Licensee Master Publishing Group http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Article Darwish, Ibrahim A. Hussein, Samiha A. Mahmoud, Ashraf M. Hassan, Ahmed I. Sensitive Indirect Spectrophotometric Method for Determination of H(2)-Receptor Antagonists in Pharmaceutical Formulations |
title | Sensitive Indirect Spectrophotometric Method for Determination of H(2)-Receptor Antagonists in Pharmaceutical Formulations |
title_full | Sensitive Indirect Spectrophotometric Method for Determination of H(2)-Receptor Antagonists in Pharmaceutical Formulations |
title_fullStr | Sensitive Indirect Spectrophotometric Method for Determination of H(2)-Receptor Antagonists in Pharmaceutical Formulations |
title_full_unstemmed | Sensitive Indirect Spectrophotometric Method for Determination of H(2)-Receptor Antagonists in Pharmaceutical Formulations |
title_short | Sensitive Indirect Spectrophotometric Method for Determination of H(2)-Receptor Antagonists in Pharmaceutical Formulations |
title_sort | sensitive indirect spectrophotometric method for determination of h(2)-receptor antagonists in pharmaceutical formulations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3614635/ https://www.ncbi.nlm.nih.gov/pubmed/23675034 |
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