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Voltammetric Determination of Cyproterone Acetate in Pharmaceutical Preparations

The voltammetric behaviour of cyproterone acetate (CPA) was studied using direct current (DC(t)) and differential pulse polarography (DPP). The drug manifests cathodic waves over the pH range of 4-11.8. In Britton-Robinson buffer (BRb) of pH 10, the diffusion current-concentration relationship was f...

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Detalles Bibliográficos
Autores principales: El-Enany, Nahed, El-Sherbiny, Dina, Belal, Fathalla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Master Publishing Group 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3614741/
https://www.ncbi.nlm.nih.gov/pubmed/23675186
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author El-Enany, Nahed
El-Sherbiny, Dina
Belal, Fathalla
author_facet El-Enany, Nahed
El-Sherbiny, Dina
Belal, Fathalla
author_sort El-Enany, Nahed
collection PubMed
description The voltammetric behaviour of cyproterone acetate (CPA) was studied using direct current (DC(t)) and differential pulse polarography (DPP). The drug manifests cathodic waves over the pH range of 4-11.8. In Britton-Robinson buffer (BRb) of pH 10, the diffusion current-concentration relationship was found to be rectilinear over the range 3.2-32 μg/mL and 0.5-14 μg/mL using DC(t) and DPP modes, respectively, with minimum limits of detection (LOD) of 0.13 μg/mL using the DDP. The diffusion-current constant (Id) was 9.29 ± 0.046 (n=9). The proposed method was successfully applied to the determination of the studied compound in its formulations. The mean percentage recoveries in tablets were 99.48 ± 1.25 and 100.01 ± 1.07 (n=4) using DC(t) and DPP modes, respectively. The results obtained were in agreement with those of the reference method. A proposal for the electrode reaction was postulated.
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spelling pubmed-36147412013-05-01 Voltammetric Determination of Cyproterone Acetate in Pharmaceutical Preparations El-Enany, Nahed El-Sherbiny, Dina Belal, Fathalla Int J Biomed Sci Article The voltammetric behaviour of cyproterone acetate (CPA) was studied using direct current (DC(t)) and differential pulse polarography (DPP). The drug manifests cathodic waves over the pH range of 4-11.8. In Britton-Robinson buffer (BRb) of pH 10, the diffusion current-concentration relationship was found to be rectilinear over the range 3.2-32 μg/mL and 0.5-14 μg/mL using DC(t) and DPP modes, respectively, with minimum limits of detection (LOD) of 0.13 μg/mL using the DDP. The diffusion-current constant (Id) was 9.29 ± 0.046 (n=9). The proposed method was successfully applied to the determination of the studied compound in its formulations. The mean percentage recoveries in tablets were 99.48 ± 1.25 and 100.01 ± 1.07 (n=4) using DC(t) and DPP modes, respectively. The results obtained were in agreement with those of the reference method. A proposal for the electrode reaction was postulated. Master Publishing Group 2010-06 /pmc/articles/PMC3614741/ /pubmed/23675186 Text en © Nahed El-Enany 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
El-Enany, Nahed
El-Sherbiny, Dina
Belal, Fathalla
Voltammetric Determination of Cyproterone Acetate in Pharmaceutical Preparations
title Voltammetric Determination of Cyproterone Acetate in Pharmaceutical Preparations
title_full Voltammetric Determination of Cyproterone Acetate in Pharmaceutical Preparations
title_fullStr Voltammetric Determination of Cyproterone Acetate in Pharmaceutical Preparations
title_full_unstemmed Voltammetric Determination of Cyproterone Acetate in Pharmaceutical Preparations
title_short Voltammetric Determination of Cyproterone Acetate in Pharmaceutical Preparations
title_sort voltammetric determination of cyproterone acetate in pharmaceutical preparations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3614741/
https://www.ncbi.nlm.nih.gov/pubmed/23675186
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