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dc.contributor.authorTabrizi, AB
dc.date.accessioned2018-08-26T08:32:57Z
dc.date.available2018-08-26T08:32:57Z
dc.date.issued2007
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52361
dc.description.abstractA new, simple, sensitive and rapid spectrofluorimetric method for the determination of piroxicam and propranolol in pharmaceutical formulations has been described. The method is based on the oxidation of piroxicam and propranolol with cerium (IV) to produce cerium (III), whose fluorescence was monitored at 352 nm while excited at 255 nm. The variables affecting oxidation of these drugs were studied and optimized. Under the experimental conditions, the calibration graphs were linear over the range of 0.02-3.0 and 0.02-2.4 mg/L, respectively, for piroxicam and propranolol. The limit of detection for piroxicam and propranolol was 0.006 and 0.008 mg/L, respectively, and the relative standard deviation of 5 replicate determinations of these drugs at 1.0 mg/L concentration level was 1.65 and 1.79%, respectively. Good recoveries in the range of 95-108% were obtained for spiked samples. The proposed methods were successfully applied to the determination of piroxicam and propranolol in commercial pharmaceutical formulations.
dc.language.isoEnglish
dc.relation.ispartofJournal of Food and Drug Analysis
dc.subjectcerium
dc.subjectpiroxicam
dc.subjectpropranolol
dc.subjectanalytic method
dc.subjectarticle
dc.subjectcalibration
dc.subjectconcentration response
dc.subjectdrug capsule
dc.subjectdrug determination
dc.subjectdrug formulation
dc.subjectdrug isolation
dc.subjectdrug monitoring
dc.subjectdrug oxidation
dc.subjectfluorescence analysis
dc.subjectprocess optimization
dc.subjectquantitative analysis
dc.subjectsensitivity analysis
dc.subjectspectrofluorometry
dc.subjecttablet formulation
dc.subjectvalidation process
dc.titleA simple spectrofluorimetric method for determination of piroxicam and propranolol in pharmaceutical preparations
dc.typeArticle
dc.citation.volume15
dc.citation.issue3
dc.citation.spage242
dc.citation.epage248
dc.citation.indexScopus


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