• 1 January 1976
    • journal article
    • research article
    • Vol. 60  (11) , 1611-1618
Abstract
A rapid and highly sensitive method is described for the quantitative determination of adriamycin (Ad) and metabolites in plasma. Ad with daunorubicin added as the internal standard was extracted from plasma with chloroform-isopropanol (1:1), separated by TLC and quantitated in situ via a fluorescence scanning technique. This method represents 1 of the very few reliable quantitative TLC methods and is suitable for the routine determination of Ad in plasma in amounts as low as 2 ng/ml. Plasma Ad levels at 24 h in rabbits and cancer patients given a 1 mg/kg dose, previously regarded as difficult to be measured, are now easily measurable using as little as 0.5 ml of plasma. Multiple samples (10-15) can be analyzed by this method within 1 day.

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