1994
DOI: 10.1016/0731-7085(93)e0022-f
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First and second derivative spectrophotometric determination of cefoperazone and sulbactam in injections

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1995
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Cited by 30 publications
(13 citation statements)
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“…The clear supernatant layer was filtrated through a 0.45 m milli-pore filter to produce a proteinfree human serum spiked with various concentrations of cefoperazone. (iv) Series of a Britton-Robinson (B-R) universal (pH [2][3][4][5][6][7][8][9][10][11] and an acetate (pH 3.6-5.5) buffers as supporting electrolytes were prepared.…”
Section: Reagents and Solutionsmentioning
confidence: 99%
See 1 more Smart Citation
“…The clear supernatant layer was filtrated through a 0.45 m milli-pore filter to produce a proteinfree human serum spiked with various concentrations of cefoperazone. (iv) Series of a Britton-Robinson (B-R) universal (pH [2][3][4][5][6][7][8][9][10][11] and an acetate (pH 3.6-5.5) buffers as supporting electrolytes were prepared.…”
Section: Reagents and Solutionsmentioning
confidence: 99%
“…These include spectrophotometry [2][3][4][5][6], spectrofluorimetry [7,8], colorimetry [9], capillary zone electrophoresis [10], high-performance liquid chromatography [11][12][13][14][15], and voltammetry [16][17][18].…”
Section: Introductionmentioning
confidence: 99%
“…The LLOQ for clavulanic acid in plasma was 1 g/ml and the precision (n = 6) at this concentration was 15.23%. The LLOQ for cefatrizine in plasma was 2 g/ml and the precision (n = 6) at this concentration was 18.22%, thus acceptable [28,29]. …”
Section: Limit Of Quantitation and Limit Of Detectionmentioning
confidence: 99%
“…The measured concentration of the proposed LLOQ should lie between 80 and 120% of its theoretical concentration and the R.S.D. should be less than 20% on a day-to-day basis [28,29]. LLOD and LLOQ were derived from multiple measurements in the low concentration range and were determined based on the signal-to-noise approach [30].…”
Section: Determination Of the Limits Of Quantitation And Detectionmentioning
confidence: 99%
“…Sulbactam analysis has been carried out in oral and injection pharmaceutical preparations using spectrophotometric, chemiluminescence, and fluorescent methods [8][9][10][11] and by capillary electrophoresis [12,13]. Many methods of analysis of sulbactam in biological fluids and pharmaceutical formulations using high performance liquid chromatography have been developed [15][16][17][18].…”
Section: Introductionmentioning
confidence: 99%