Spectrophotometric Assay of Bromhexine hydrochloride in Pure and in Pharmaceutical Dosage Forms by Diazometry Coupling Reaction
Author(s) -
Salim Mohammed,
Rana F. Almukhtar
Publication year - 2013
Publication title -
mağallaẗ al-tarbiyaẗ wa-al-ʻilm
Language(s) - English
Resource type - Journals
eISSN - 2664-2530
pISSN - 1812-125X
DOI - 10.33899/edusj.2013.163069
Subject(s) - molar absorptivity , chemistry , dosage form , detection limit , hydrochloric acid , reagent , chromatography , hydrochloride , benzoic acid , pharmaceutical formulation , spectrophotometry , absorption (acoustics) , sodium nitrite , nuclear chemistry , organic chemistry , materials science , physics , optics , composite material
A simple, accurate and sensitive spectrophotometric method has been developed for quantitative determination of bromhexine hydrochloride (BH) in both pure form and in its pharmaceutical preparations. The proposed method is based on the diazotization of BH with sodium nitrite in hydrochloric acid medium to form diazonium salt , Spectrophotometric Assay of Bromhexine hydrochloride in Pure and .... 198 which is coupled with 2,4,6-trihydroxy benzoic acid in alkaline medium of sodiumHydroxide to form a stable and water-soluble azo dye exhibited absorption maximum at 408 nm against reagent blank. Beer’s law is obeyed over the concentration range of 5 to750 μg of BH/20 ml with a good determination coefficient ( R=0.9973) and apparent molar absorptivity 3.053×10 l.mol.cm. The limit of detection (LOD) and limit of quantification (LOQ) are 0.0156 and 0.0520 μg ml, respectively. The relative errors and relative standard deviations are found as 0.19 – 1.42 % and ± 0.11 to ± 0.47% respectively, depending on the concentration level. The method is suitable for the determination of BH in the presence of other ingredients that are usually present in dosage forms. The composition of the resulting product has been also worked out and it is found to be (1:1) BH : 2,4,6-tri-hydroxybenzoic acid. This procedure is applied successfully for the analysis of BH in pharmaceutical preparations (tablets, syrup and injection) without prior separation and with acceptable errors.
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