Abstract
Purpose: To develop a simple, accurate, and precise high performance chromatography (HPLC) method with spectrophotometric detection for the determination of doxorubicin hydrochloride in rat plasma.
Methods: Doxorubicin hydrochloride and daunorubicin hydrochloride (internal standard, IS) were separated on a C-18 reversed-phase HPLC column. Following protein precipitation extraction, chromatographic separation was accomplished with a mobile phase consisting of acetonitrile: water at ratio of 30: 70 (pH 3.0), and the drug was detected at 233 nm using a UV detector at flow rate of 1.0 ml/min and ambient temperature.
Results: Linearity was obtained over the range 1.0 - 50.0 mu g/ml for doxorubicin hydrochloride with lower limit of quantitation of 1.0 mu g/ml. For each level of quality control samples, inter-and intra- day precision (% CV) was < 9.6 and 5.1 %, respectively. Stability of doxorubicin hydrochloride in plasma was within the acceptance limit (+/- 15 %) with no evidence of degradation during sample processing and 30 days storage in a deep freezer at - 70 +/- 5 C. Absolutes extraction recovery of drug from plasma was >= 86 %.
Conclusion: The method is highly selective and rugged for the determination of doxorubicin hydrochloride in rat plasma and should be suitable for conducting pharmacokinetic studies and therapeutic drug monitoring.