RT Journal Article
SR Electronic
T1 PKP-017 Doxorubicin plasma determination by high performance liquid chromatography
JF European Journal of Hospital Pharmacy
JO Eur J Hosp Pharm
FD British Medical Journal Publishing Group
SP A200
OP A201
DO 10.1136/ejhpharm-2017-000640.445
VO 24
IS Suppl 1
A1 Ros, L Casamada
A1 Vergara, B Quintana
A1 Alcaraz, A Sanchez
YR 2017
UL http://ejhp.bmj.com/content/24/Suppl_1/A200.3.abstract
AB Background Doxorubicin (DXR) is used in the treatment of hepatocarcinoma. Transarterial chemoembolisation is a drug delivery technique that allows reduction of its concentration in plasma, increases the quality of life for patients and improves their response to treatment.Purpose To assess and validate the chromatographic conditions for determining plasma DXR. Linearity, accuracy, precision and reproducibility inter- and intra-assay were studied.Material and methods The test products used were daunorubicin (internal standard) and DXR (standard substance). The reagents used were potassium dihydrogen phosphate, acetonitrile, water and isopropanol. Free human plasma drug was provided by the hospital laboratory analysis. Equipment used in the study: a modular system of high performance liquid chromatography (HPLC) Merck-Hitachi composed of a pump, autoinjector system, fluorescence detector, integrating software and a computer. A centrifuge and a vortex were also used. The stationary phase used was a 5.mu.m C18 chromatographic column 150 mm × 4 mm, and the selected mobile phase was 0.05 M potassium dihydrogen phosphate (pH=3.55) and acetonitrile 70:30 (v/v). The flow rate chosen was 0.6 mL/min and the wavelengths of excitation and emission were 548 nm and 470 nm.Results The equation of the calibration curve (peak area and plasma DXR) was: y=−256.34 + 1231.27 x. The analytical technique had good linearity. With 95% confidence it can be said that the intercept was between 162.4 and 350.3 area/C. With a probability of 99.5% the value obtained and the actual value were not statistically different, therefore the method has the necessary accuracy. The requirements of precision (repeatability and reproducibility) were also met. The coefficients of variation of plasma concentrations did not exceed 10% for either intra or inter studies (repeatability and reproducibility).Conclusion The chromatographic technique developed to determine plasma DXR is a quick and simple technique that meets all of the requirements of specificity, linearity, accuracy and precision required for validation.References and/or acknowledgements Escudero-Ortiz V, Ramón-López A, Duart MJ, et al. Populational pharmacokinetics of doxorubicin applied to personalised its dosing in cancer patients. Farmacia Hospitalaria2012;36(04).Wood MJ. Photodegradation of doxorubicin, daunorubicin and epirubicin measured by high performance liquid chromatography. J Clin Pharm Ther 1990;15:291–300.No conflict of interest