This is the authors' abstract. We don't add key points for this paper.
We developed two fast, simple and sensitive spectrophotometric methods for the determination of ceftazidime in drugs by using phenolic reagents resorcinol and 2-methylphenol. The methods are based on a previous antibiotic diazotization in the medium of hydrochloric acid (CHCl=12 M) and its following azo coupling with reagents in an alkaline medium with the formation of effective analytical forms that allow determining ceftazidime and have maximum absorbance at 519 nm and 516 nm for resorcinol and 2- methylphenol, respectively. The azo coupling products of diazotized ceftazidime exhibit effective molar absorptivity in the range of (6.31–6.84)103 M–1 cm–1. Stoichiometric ratios of the azo compounds components were established using continuous variations methods and they were the same in both cases (1:1). The developed methods allow determining from 2.75 to 185.5 g mL–1 of ceftazidime with resorcinol (LOQ=2.54 g mL–1) and 0.32191.3 g mL–1 of ceftazidime with 2-methylphenol (LOQ=0.28 g mL–1). The developed methods have been successfully tested in the analyses of one-component preparations (powders for injection solutions).
Answers are grounded in this paper and cite their sources.
No takes yet. Share an insight, caveat, or question.
Kostiv et al. (2021) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: