Mc. Price et Dw. Hoffman, THERAPEUTIC DRUG-MONITORING OF RISPERIDONE AND 9-HYDROXYRISPERIDONE IN SERUM WITH SOLID-PHASE EXTRACTION AND HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY, Therapeutic drug monitoring, 19(3), 1997, pp. 333-337
This laboratory developed a simple and efficient solid-phase extractio
n method that is combined with high-performance liquid chromatography
for rapid and precise therapeutic monitoring of risperidone (Risperdal
) in blood concentrations. The solid-phase extraction uses a mixed bed
column. Sensitivity of the chromatographic method is 0.5 ng/ml (180 p
mol/ml) of drug in serum, and separations can be performed in a 15-min
ute chromatographic run. Advantages of this approach include enhanced
speed, sensitivity, and efficiency. A high level of sensitivity may be
achieved because of the absence of interference from other drugs, met
abolites, or serum components.