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dc.contributor.authorManzoori, JL
dc.contributor.authorAmjadi, M
dc.contributor.authorSoltani, N
dc.contributor.authorJouyban, A
dc.date.accessioned2018-08-26T06:04:58Z
dc.date.available2018-08-26T06:04:58Z
dc.date.issued2014
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/41630
dc.description.abstractCefixime (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.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.The maximum response was achieved under optimum conditions of [Tris buffer]= 0.008 mol/l (pH 6.5), [Tb(3+)]=1أ—10(-4) mol/l and [Dano]=1أ—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 8.8أ—10(-8)-8.8أ—10(-7) mol/l and 1.1أ—10(-7)-8.8أ—10(-7) mol/l in standard and human serum samples with the detection limits (S/N=3) of 2.8أ—10(-8) mol/l and 3.9أ—10(-8) mol/l, respectively. The Cfx was determined in pharmaceutical tablets and spiked serum samples and the results were satisfactory.This method is simple, practical and relatively interference-free for determination of Cfx in pharmaceutical tablets and serum samples.
dc.language.isoEnglish
dc.relation.ispartofIranian journal of basic medical sciences
dc.titleSpectrofluorimetric determination of cefixime using terbium-danofloxacin probe.
dc.typearticle
dc.citation.volume17
dc.citation.issue4
dc.citation.spage256
dc.citation.epage62
dc.citation.indexPubmed


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