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Spectrofluorimetric determination of cefixime using terbium-danofloxacin probe

OBJECTIVE(S): Cefixime (Cfx), is a semi-synthetic third-generation oral cephalosporin antibiotic that is prescribed for the treatment of susceptible infections. There are some procedures for the determination of Cfx in pharmaceutical formulations and biological samples. Herein a spectrofluorimetric...

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Autores principales: Manzoori, Jamshid L., Amjadi, Mohammad, Soltani, Naser, Jouyban, Abolghasem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046237/
https://www.ncbi.nlm.nih.gov/pubmed/24904718
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author Manzoori, Jamshid L.
Amjadi, Mohammad
Soltani, Naser
Jouyban, Abolghasem
author_facet Manzoori, Jamshid L.
Amjadi, Mohammad
Soltani, Naser
Jouyban, Abolghasem
author_sort Manzoori, Jamshid L.
collection PubMed
description OBJECTIVE(S): Cefixime (Cfx), is a semi-synthetic third-generation oral cephalosporin antibiotic that is prescribed for the treatment of susceptible infections. There are some procedures for the determination of Cfx in pharmaceutical formulations and biological samples. Herein a spectrofluorimetric method was proposed for Cfx determination based on the fluorescence quenching of terbium-danofloxacin (Tb(3+)-Dano) in the presence of Cfx. MATERIALS AND METHODS: Cfx was detected based on fluorescence quenching of terbium-danofloxacin (Tb(3+)-Dano) in the presence of Cfx with maximum excitation and emission wavelengths at 347 nm and 545 nm, respectively. The quenched fluorescence intensity of Tb(3+)- Dano system is proportional to the concentration of Cfx. The optimum conditions for the determination of Cfx were studied. RESULTS: The maximum response was achieved under optimum conditions of [Tris buffer]= 0.008 mol/l (pH 6.5), [Tb(3+)]=1×10(-4) mol/l and [Dano]=1×10(-4) mol/l. The developed method was evaluated in terms of accuracy, precision and limit of detection. The linear concentration ranges for quantification of Cfx were 8.8×10(-8)-8.8×10(-7) mol/l and 1.1×10(-7)-8.8×10(-7) mol/l in standard and human serum samples with the detection limits (S/N=3) of 2.8×10(-8) mol/l and 3.9×10(-8) mol/l, respectively. The Cfx was determined in pharmaceutical tablets and spiked serum samples and the results were satisfactory. CONCLUSION: This method is simple, practical and relatively interference-free for determination of Cfx in pharmaceutical tablets and serum samples.
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spelling pubmed-40462372014-06-05 Spectrofluorimetric determination of cefixime using terbium-danofloxacin probe Manzoori, Jamshid L. Amjadi, Mohammad Soltani, Naser Jouyban, Abolghasem Iran J Basic Med Sci Original Article OBJECTIVE(S): Cefixime (Cfx), is a semi-synthetic third-generation oral cephalosporin antibiotic that is prescribed for the treatment of susceptible infections. There are some procedures for the determination of Cfx in pharmaceutical formulations and biological samples. Herein a spectrofluorimetric method was proposed for Cfx determination based on the fluorescence quenching of terbium-danofloxacin (Tb(3+)-Dano) in the presence of Cfx. MATERIALS AND METHODS: Cfx was detected based on fluorescence quenching of terbium-danofloxacin (Tb(3+)-Dano) in the presence of Cfx with maximum excitation and emission wavelengths at 347 nm and 545 nm, respectively. The quenched fluorescence intensity of Tb(3+)- Dano system is proportional to the concentration of Cfx. The optimum conditions for the determination of Cfx were studied. RESULTS: The maximum response was achieved under optimum conditions of [Tris buffer]= 0.008 mol/l (pH 6.5), [Tb(3+)]=1×10(-4) mol/l and [Dano]=1×10(-4) mol/l. The developed method was evaluated in terms of accuracy, precision and limit of detection. The linear concentration ranges for quantification of Cfx were 8.8×10(-8)-8.8×10(-7) mol/l and 1.1×10(-7)-8.8×10(-7) mol/l in standard and human serum samples with the detection limits (S/N=3) of 2.8×10(-8) mol/l and 3.9×10(-8) mol/l, respectively. The Cfx was determined in pharmaceutical tablets and spiked serum samples and the results were satisfactory. CONCLUSION: This method is simple, practical and relatively interference-free for determination of Cfx in pharmaceutical tablets and serum samples. Mashhad University of Medical Sciences 2014-04 /pmc/articles/PMC4046237/ /pubmed/24904718 Text en Copyright: © Journal Management System. Created by sinaweb http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Manzoori, Jamshid L.
Amjadi, Mohammad
Soltani, Naser
Jouyban, Abolghasem
Spectrofluorimetric determination of cefixime using terbium-danofloxacin probe
title Spectrofluorimetric determination of cefixime using terbium-danofloxacin probe
title_full Spectrofluorimetric determination of cefixime using terbium-danofloxacin probe
title_fullStr Spectrofluorimetric determination of cefixime using terbium-danofloxacin probe
title_full_unstemmed Spectrofluorimetric determination of cefixime using terbium-danofloxacin probe
title_short Spectrofluorimetric determination of cefixime using terbium-danofloxacin probe
title_sort spectrofluorimetric determination of cefixime using terbium-danofloxacin probe
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046237/
https://www.ncbi.nlm.nih.gov/pubmed/24904718
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