FIELD: medicine; therapy; toxicology.
SUBSTANCE: invention can be used for determination of medicinal substances in urine, saliva or blood plasma. Samples of determined substances in solution and samples of witness substances are chromatographed in a thin layer of sorbent. Test solution is prepared from 10 ml of urine, saliva or blood plasma by isolation with 40 ml of ethyl acetate with successive change of pH: pH=3.0, then pH=10.0 using buffer solutions. Chromatography is carried out on Sorbfil plates in a system of solvents dioxane—chloroform—acetone—25% ammonia solution in a volume ratio of 40:40:6:3 and determination of zones of substances on chromatogram in UV light at wave length 254 nm. Mobility factor Rf is determined. If Rf values are 0.4±0.01, perchlozon is determined, 0.79±0.01—rifabutin, 0.1±0.01—ftivazide, 0.46±0.01—pyrazinamide, 0.37±0.01—linezolid, 0.02±0.01—levofloxacin, 0.56±0.01—prothionamide, 0.24±0.01—abacavir, 0.71±0.01—amitriptyline, 0.3±0.01—phenobarbital, 0.75±0.01—aminazin, 0.35±0.01—metronidazole, 0.85±0.01—cinnarizine, 0.5±0.01—analgin.
EFFECT: method provides higher selectivity, objectivity and sensitivity of analysis in urine, saliva or blood plasma of medicinal substances due to the fact that ethyl acetate is used as a solvent for isolating medicinal substances with successive pH change: pH 3, then pH 10, and chromatography is carried out in the system dioxane—chloroform—acetone—25% ammonia in ratio 40:40:6:3.
1 cl, 1 ex
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Authors
Dates
2024-10-21—Published
2023-12-14—Filed