ABSTRACT
Reversed-phase high-performance liquid chromatographic (HPLC) procedures are described for determining the stability of 2',3'-dideoxyadenosine (DDA) in biological fluids at therapeutic dosages. The validated methodology uses both direct injection and solid-phase extraction techniques. Deamination of DDA to 2',3'-dideoxyinosine (DDI) in plasma by adenosine deaminase was monitored by HPLC, and the identification of DDI verified by thermospray HPLC-mass spectrometry. This methodology should prove useful in future studies concerning the stability and metabolism of dideoxynucleosides.
Subject(s)
Chromatography, High Pressure Liquid/methods , Deoxyadenosines/analogs & derivatives , Adenosine Deaminase/pharmacology , Animals , Deoxyadenosines/blood , Dideoxyadenosine , Humans , Mass Spectrometry , MiceABSTRACT
Allylglucosinolate, found in many cruciferous plants, is acutely toxic to Papilio polyxenes larvae, which do not normally attack crucifers. By contrast, larval growth of Pieris rapae, a crucifer specialist, is not affected even by artificially high concentrations of allylglucosinolate. Larval growth of Spodoptera eridania, a generalist feeder, is inhibited by high but not by low concentrations of the compound.