Abstract
A sensitive and specific method for the determination of chlorambucil and its metabolite in biological fluids is reported. The method is based on selected-ion monitoring detection following simple extraction of the parent compound, its metabolite, and an internal standard (chlorambucil-d8) from plasma and urine samples. The precision (reproducibility) of the method was 94.3 ± 1.3% with 200ng of chlorambucil added to 1ml of plasma. Chlorambucil degradation or alkylation of plasma proteins was minimal with plasma incubated at 24° for 4hr. However, chloroambucil recovery decreased to 56% after plasma incubation at 37° for 4hr. Three chlorambucil degradation products in ethyl acetate solution were found, and their structures were studied by mass spectrometry.
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