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Spectrophotometric determination of imipramine HCl in pure and pharmaceutical forms | Abstract

Der Pharma Chemica
Journal for Medicinal Chemistry, Pharmaceutical Chemistry, Pharmaceutical Sciences and Computational Chemistry

ISSN: 0975-413X
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Abstract

Spectrophotometric determination of imipramine HCl in pure and pharmaceutical forms

Author(s): K. Susmitha, M. Thirumalachary, T. Vinod Kumar and G. Venkateshwarlu

Six spectrophotometric methods, A, B, C, D, E and F for the determination of Imipramine HCl have been developed, validated and applied for the assay of the drug in pharmaceuticals. Methods A, B, C and D are based on ion pair complexation of drug, in acidic buffers, with triphenylmethane dyes viz., Bromothymol blue (BTB), Bromophenol blue (BPB), Bromocresol green (BCG) and Bromocresol purple (BCP). The complexes are extracted into chloroform and absorbance is measured around 415 nm as a function of concentration of the drug. The stoichiometry of each of the complex is found be 1:1. Method E depends upon charge transfer complexation of neutralized drug with iodine which produces iodide ion whose absorbance at 366 nm is measured as function of concentration of the drug. This complex, too, has 1:1 composition as determined by Job’s method. Method F is developed on the basis of oxidation of the drug with alkaline KMnO4 which generates green colored manganate ion with λmax 610 nm. As the intensity of green color increased with increasing time, kinetics of the reaction is followed and calibration curves are constructed by using initial rate and fixed time methods. Excellent recovery studies with high accuracy and precision indicate that the methods can be successfully used in industries for the assay of drug in pure and pharmaceutical forms.


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