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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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Detalles Bibliográficos
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
Descripción
Sumario: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.