A sensitive and specific high-performance liquid chromatographic method for the identification and quantitation of chlorophacinone in animal tissues has been developed. Residues were extracted with chloroform-acetone (1: 1, v/v). Clean-up of extracts was accomplished with a combined gel permeation-
Reversed-phase ion-pair chromatographic method for the determination of nitroprusside in photolyzed solutions
โ Scribed by O.R. Leeuwenkamp; E.J. van Mark; P.M. van der Klauw; W.P. van Bennekom; A. Bult
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 565 KB
- Volume
- 161
- Category
- Article
- ISSN
- 0003-2670
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โฆ Synopsis
A rapid reversed-phase ion-pair chromatographic method for disodium pentacyanonitrosylferrate(I1) (nitroprusside) and its photodegradation products nitrite, nitrate, hexacyanoferrate(I1) and hexacyanoferrate(II1) is described. For chromatography, phenyl-bonded pellicular silica gel (10 pm) was used with a mobile phase consisting of water (0.005 M tetrabutylammonium phosphate, 0.0011 M n-octylamine, 0.01 M potassium dihydrogenphosphate, pH 7.0) and methanol (0.005 M tetrabutylammonium phosphate, 0.0011 M n-octylamine) (65:35); the detector was set at 220 nm. In 5% (w/v) dextrose solutions, the calibration graph for nitroprusside was linear over the concentration range lo-120 pg ml-'. A qualitative explanation for the order of retention: hexacyanoferrate( II) < hexacyanoferrate( III) < nitroprusside is given. The method is suitable for the selective determination of nitroprusside in photolyzed infusion solutions (100 pg ml-' in aqueous 5% dextrose) and gives an impression of the decomposition products formed.
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