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Determination of Cefixime by a Validated Stability-Indicating HPLC Method and Identification of its Related Substances by LC-MS/MS Studies

Cefixime is an important cephalosporin antibiotic that easily decomposes and releases different related substances in preparation and storage steps. The objective of the current study was to develop a simple, precise, and accurate isocratic liquid chromatography (LC) method for the determination of...

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Autores principales: Talebpour, Zahra, Pourabdollahi, Hakimeh, Rafati, Hasan, Abdollahpour, Asem, Bashour, Yusef, Aboul-Enein, Hassan Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Österreichische Apotheker-Verlagsgesellschaft 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3700077/
https://www.ncbi.nlm.nih.gov/pubmed/23833715
http://dx.doi.org/10.3797/scipharm.1301-15
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author Talebpour, Zahra
Pourabdollahi, Hakimeh
Rafati, Hasan
Abdollahpour, Asem
Bashour, Yusef
Aboul-Enein, Hassan Y.
author_facet Talebpour, Zahra
Pourabdollahi, Hakimeh
Rafati, Hasan
Abdollahpour, Asem
Bashour, Yusef
Aboul-Enein, Hassan Y.
author_sort Talebpour, Zahra
collection PubMed
description Cefixime is an important cephalosporin antibiotic that easily decomposes and releases different related substances in preparation and storage steps. The objective of the current study was to develop a simple, precise, and accurate isocratic liquid chromatography (LC) method for the determination of cefixime in the presence of its related substances generated from thermal stress in the bulk drug. The chromatographic conditions were comprised of a reversed-phase C18 column (4.6 × 250 mm, 5 μm) with a mobile phase composed of water: acetonitrile (85:15 v/v, with 0.5% formic acid) and ultraviolet detection (UV). Some thermal degradation products were identified using a proposed liquid chromatography-mass spectrometry method. Five peaks (A, B, C, D, and E impurities based on British Pharmacopoeia) were known and a few unknown peaks appeared in the thermal stress solution of cefixime. The linear regression analysis data for the calibration plot of the LC-UV method showed a good linear relationship in the concentration range 0.9–1000.0 μg mL(−1). The recovery of the optimized method was between 94.6 and 98.4% and the inter- and intra-day relative standard deviations were less than 3.3%. The obtained results shown in the LC-UV proposed method can be conveniently used in a quality control laboratory for routine analysis of cefixime for the assay and related substances, as well as for the evaluation of stability samples of bulk drugs.
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spelling pubmed-37000772013-07-05 Determination of Cefixime by a Validated Stability-Indicating HPLC Method and Identification of its Related Substances by LC-MS/MS Studies Talebpour, Zahra Pourabdollahi, Hakimeh Rafati, Hasan Abdollahpour, Asem Bashour, Yusef Aboul-Enein, Hassan Y. Sci Pharm Research Article Cefixime is an important cephalosporin antibiotic that easily decomposes and releases different related substances in preparation and storage steps. The objective of the current study was to develop a simple, precise, and accurate isocratic liquid chromatography (LC) method for the determination of cefixime in the presence of its related substances generated from thermal stress in the bulk drug. The chromatographic conditions were comprised of a reversed-phase C18 column (4.6 × 250 mm, 5 μm) with a mobile phase composed of water: acetonitrile (85:15 v/v, with 0.5% formic acid) and ultraviolet detection (UV). Some thermal degradation products were identified using a proposed liquid chromatography-mass spectrometry method. Five peaks (A, B, C, D, and E impurities based on British Pharmacopoeia) were known and a few unknown peaks appeared in the thermal stress solution of cefixime. The linear regression analysis data for the calibration plot of the LC-UV method showed a good linear relationship in the concentration range 0.9–1000.0 μg mL(−1). The recovery of the optimized method was between 94.6 and 98.4% and the inter- and intra-day relative standard deviations were less than 3.3%. The obtained results shown in the LC-UV proposed method can be conveniently used in a quality control laboratory for routine analysis of cefixime for the assay and related substances, as well as for the evaluation of stability samples of bulk drugs. Österreichische Apotheker-Verlagsgesellschaft 2013 2013-02-18 /pmc/articles/PMC3700077/ /pubmed/23833715 http://dx.doi.org/10.3797/scipharm.1301-15 Text en © 2013 Talebpour et al.; licensee Österreichische Apotheker-Verlagsgesellschaft m. b. H., Vienna, Austria. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Talebpour, Zahra
Pourabdollahi, Hakimeh
Rafati, Hasan
Abdollahpour, Asem
Bashour, Yusef
Aboul-Enein, Hassan Y.
Determination of Cefixime by a Validated Stability-Indicating HPLC Method and Identification of its Related Substances by LC-MS/MS Studies
title Determination of Cefixime by a Validated Stability-Indicating HPLC Method and Identification of its Related Substances by LC-MS/MS Studies
title_full Determination of Cefixime by a Validated Stability-Indicating HPLC Method and Identification of its Related Substances by LC-MS/MS Studies
title_fullStr Determination of Cefixime by a Validated Stability-Indicating HPLC Method and Identification of its Related Substances by LC-MS/MS Studies
title_full_unstemmed Determination of Cefixime by a Validated Stability-Indicating HPLC Method and Identification of its Related Substances by LC-MS/MS Studies
title_short Determination of Cefixime by a Validated Stability-Indicating HPLC Method and Identification of its Related Substances by LC-MS/MS Studies
title_sort determination of cefixime by a validated stability-indicating hplc method and identification of its related substances by lc-ms/ms studies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3700077/
https://www.ncbi.nlm.nih.gov/pubmed/23833715
http://dx.doi.org/10.3797/scipharm.1301-15
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