1982
DOI: 10.1039/an9820701451
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High-performance liquid chromatographic determination of cefuroxime

Abstract: A rapid, precise and selective method is described for determining the purity of cefuroxime sodium. Cefuroxime is separated from closely related compounds by high-performance liquid chromatography a t ambient temperature using a 10-cm column packed with 5-,urn Spherisorb C6 and buffered aqueous acetonitrile as mobile phase. The eluate is monitored a t 273 nm, orcinol is used as internal standard and the method has a coefficient of variation of 0.6%. The procedure is suitable for the analysis of freshly manufac… Show more

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Cited by 14 publications
(3 citation statements)
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“…Atomic absorption procedure based on the reaction with silver nitrate/lead acetate at pH 7 [8] and, spectrophotometric methods after complexation with 7,7,8,8-tetracyanoquinodimethane, p-chloranilic acid, Prussian Blue and reaction with metol-chromium (VI) reagent [9,10] have been explored. Flow-injection analysis [11], capillary electrophoresis [12,13], liquid chromatography [14,15] and the analysis of injectible by UV and HPLC are also known for analysis [16].…”
Section: Introductionmentioning
confidence: 99%
“…Atomic absorption procedure based on the reaction with silver nitrate/lead acetate at pH 7 [8] and, spectrophotometric methods after complexation with 7,7,8,8-tetracyanoquinodimethane, p-chloranilic acid, Prussian Blue and reaction with metol-chromium (VI) reagent [9,10] have been explored. Flow-injection analysis [11], capillary electrophoresis [12,13], liquid chromatography [14,15] and the analysis of injectible by UV and HPLC are also known for analysis [16].…”
Section: Introductionmentioning
confidence: 99%
“…Key:( 8 ) isomer B syn; (0) isomer A syn, (e) isomer €3 anti, (0) isomer A antt (W) isomer B syn kept in the dark; ( 0 ) isomer A syn kept in the dark.respective couples of diastereomers for I and I1 were separated. Typical capacity factors were 6.1 (Id, 5.1 (Id, 13.1 (IIA),10.6 (IIB), 6.9 (I& and I&), and 0.9 (IV).The linearity of the calibration graphs (height-concentration) was assessed by injecting six mixed standard solutions ranging between 2 X 10-4 and 2 x 10-5 M for each compound. The graph was linear (r > 0.999) and went through the origin (p = 0.05) in all cases.The repeatability of the chromatographic system was assessed at two different concentrations (2 X 10" and 2 X 1W M).…”
mentioning
confidence: 99%
“…(SALEM e ASKAL, 2002) e a espectrofotometria (absorção atômica, absorção no visível (MAHMOUD et al, 2009;AMIN e RAGABB, 2004;AYAD et al, 1999;OKOYE et al, 2007) além da eletroforese capilar (SCIACCHITANO et al, 1994;PAJCHEL & TYSKI, 2000), e da cromatografia líquida de alta eficiência (COOMBER et al, 1982;ZIVANOVIC et at., 2004;RODENBACH et al, 2006).…”
Section: Metodologia Analíticaunclassified