Oxidized diphenylamine is newly utilized as a redox spectrophotometric reagent for the
d
etermination of six pharmaceutically important thiol and thioamide drugs named:
acetylcystiene, captopril, carbimazole, propylthiouracil, thiopental sodium, and tiopronin. The
meth
od is based on measurement of the decrease in absorption intensify of the oxidized
diphenylamine (d
iphenylbenzidine violet, Lmax= 580 nm) reagent as a result of the reduction
eff
ect of the analysed drugs, This reagent was instantaneously prepared by the oxidation of
d
iphenylamine using ferric sulphate in sulphuric acid medium. The molar ratio of the
chromogen reagent was determined to be 2: 1; diphenylamine: iron (111). The decrease in
colour inte
nsity was found to be quantitatively dependant on drug concentration. Experimental
variables including reagent concentration, acid type and concentration, dilution solvent,
reaction time, temperature and stability were studied and optimized. Validation parameters
in
cluding linearity range, detection and quantitation limits, precision, selectivity and robustness
we
re evaluated. The proposed method was found to be simple, sensitive and accurate one
indicated by the studied validation parameters. Good recoveries (98.0:tO.14 - 100%, :to.98)
were obtained by the suggested method and it was applied for the determination of the studied
drugs in many pharmaceutical dosage forms available in the local market. Good agreement,
i
ndicated by acceptable t- & F- tests, was found between results obtained by the suggested
method and those obtained by the reported or pharmacopoeial methods