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J Chromatogr ; 225(1): 107-14, 1981 Sep 11.
Article in English | MEDLINE | ID: mdl-7028767

ABSTRACT

Two reversed-phase high-performance liquid chromatographic systems are presented for the separation and assay of the pyridinium aldoximes benzyl-P2A, HI-6 and obidoxime in aqueous solutions and biological samples. The systems involve a 5-micrometer C18 silica gel stationary phase. The eluent consists of methanol, acetic acid buffer (pH 4.80), a counter ion (per-chlorate or n-octanesulphonate) and a surfactant. The compounds were detected spectrophotometrically at 304 nm. In the concentration range used, linear plots of concentration versus extinction were obtained, both in blood and in water. Detection limits plots of concentration versus extinction were obtained, both in blood and in water. Detection limits, even in blood are satisfactory (0.5-1 microM). Evidence of presented that, at least for HI-6, the addition of counter ions to the system does not lead to the formation of ion pairs to be retained by partition, but rather to a mechanism based on adsorption chromatography.


Subject(s)
2,2'-Dipyridyl/blood , Pralidoxime Compounds/blood , Pyridines/blood , 2,2'-Dipyridyl/administration & dosage , 2,2'-Dipyridyl/analogs & derivatives , Animals , Chromatography, High Pressure Liquid/methods , Obidoxime Chloride/administration & dosage , Obidoxime Chloride/analogs & derivatives , Obidoxime Chloride/blood , Pralidoxime Compounds/administration & dosage , Rats , Rats, Inbred Strains
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