Utilization of oxidation reactions for the spectrophotometric determination of captopril using brominating agents

Faculty Science Year: 2010
Type of Publication: Article Pages: 1138-1145
Authors: DOI: 10.1016/j.saa.2009.12.075
Journal: SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY PERGAMON-ELSEVIER SCIENCE LTD Volume: 75
Research Area: Spectroscopy ISSN ISI:000275584000031
Keywords : Redox reactions, Bromate-bromide mixture, Spectrophotometry, Captopril, Pharmaceutical formulations    
Abstract:
Three simple, accurate and sensitive methods (A-C) for the spectrophotometric assay of captopril (CPL) in bulk drug, in dosage forms and in the presence of its oxidative degradates have been described. The methods are based on the bromination of captopril with a solution of excess brominating mixture in hydrochloric acid medium. After bromination, the excess brominating mixture is followed by the estimation of surplus bromine by three different reaction schemes. In the first method (A), the determination of the residual bromine is based on its ability to bleach the indigo carmine dye and measuring the absorbance at 610 nm. Method B, involves treating the unreacted bromine with a measured excess of iron(II) and the remaining iron(II) is complexed with 1,10-phenanthroline and the increase in absorbance is measured at 510 nm. In method (C), the surplus bromine is treated with excess of iron(II) and the resulting iron(III) is complexed with thiocyanate and the absorbance is measured at 478 nm. In all the methods, the amount of bromine reacted corresponds to the drug content. The different experimental parameters affecting the development and stability of the color are carefully studied and optimized. Beer's law is valid within a concentration range of 0.4-6.0, 0.4-2.8 and 1.2-4.8 mu g mL(-1) for methods A, B and C, respectively. The calculated apparent molar absorptivity was found to be 5.16 x 10(4), 9.95 x 10(4) and 1.74 x 10(5) L mol(-1) cm(-1), for methods A, B and C, respectively. Sandell's sensitivity, correlation coefficients, detection and quantification limits are also reported. No interference was observed from common additives found in pharmaceutical preparations. The proposed methods are successfully applied to the determination of CPL in the tablet formulations with mean recoveries of 99.94-100.11\% and the results were statistically compared with those of a reference method by applying Student's t- and F-test. (C) 2010 Elsevier B.V. All rights reserved.
   
  Online    
PDF  
       
Tweet