1985
DOI: 10.1016/s0021-9673(01)81918-x
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Determination of paracetamol, salicylic acid and acetyl salicylic acid in serum by high-performance liquid chromatography

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Cited by 22 publications
(2 citation statements)
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“…Three extraction solvents were used in order to compare the extraction efficiency of triflusal and HTB from plasma. Solvent A was acetonitrile-chloroform (40:60, v/v) [5], solvent B was diethylether [2] and solvent C was tert-butyl methyl ether (TBME) [6]. For a human plasma sample (0.5 ml), an aliquot of 100 l of the IS (1 g/ml of furosemide) and 200 l of 0.1 M hydrochloric acid were immediately added and mixed with vortex-mixer for 30 s. For a rat plasma sample (0.1 ml), an aliquot of 100 l of the IS (0.5 g/ml of furosemide) and 100 l of 0.1 M hydrochloric acid were used and mixed.…”
Section: Extraction Proceduresmentioning
confidence: 99%
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“…Three extraction solvents were used in order to compare the extraction efficiency of triflusal and HTB from plasma. Solvent A was acetonitrile-chloroform (40:60, v/v) [5], solvent B was diethylether [2] and solvent C was tert-butyl methyl ether (TBME) [6]. For a human plasma sample (0.5 ml), an aliquot of 100 l of the IS (1 g/ml of furosemide) and 200 l of 0.1 M hydrochloric acid were immediately added and mixed with vortex-mixer for 30 s. For a rat plasma sample (0.1 ml), an aliquot of 100 l of the IS (0.5 g/ml of furosemide) and 100 l of 0.1 M hydrochloric acid were used and mixed.…”
Section: Extraction Proceduresmentioning
confidence: 99%
“…Mobile phase A consisted of a mixture of 50% methanol and 0.005 M dilution of n-tetrabutyl ammonium phosphate (PIC A, Waters, Millipore, Milford, MA, USA) [2][3][4]. Mobile phase B was consisted of acetonitrile-methanol-water (25:10:65, v/v/v) adjusted to pH 2.5 with 85% (w/v) orthophosphoric acid [5]. All separations were performed isocratically at a flow-rate of 1.0 ml/min.…”
Section: Chromatographymentioning
confidence: 99%