NOVEL ASSAY-METHOD FOR MITOXANTRONE IN PLASMA, AND ITS APPLICATION IN CANCER-PATIENTS

被引:17
作者
HU, OYP
CHANG, SP
SONG, YB
CHEN, KY
LAW, CK
机构
[1] VET GEN HOSP,CTR CANC THERAPY,TAIPEI,TAIWAN
[2] TRI SERV GEN HOSP,DEPT PHARM,TAIPEI,TAIWAN
来源
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS | 1990年 / 532卷 / 02期
关键词
D O I
10.1016/S0378-4347(00)83783-4
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Mitoxantrone is an anthracene derivative that acts as a cytostatic in a variety of cancers. A quantitative analytical method has been established for the determination of mitoxantrone in plasma. The method employed C18 reversed-phase ion-pair chromatography with an isocratic mobile phase of 50.0% methanol in 10 mM phosphate buffer (pH 3.0) plus 0.09% 1-pentanesulphonic acid and ultraviolet detection. Sample preparation consisted of two extraction steps using same organic solvent system at different pH to remove plasma impurities efficiently. Potential adsorption of mitoxantrone onto glassware was considered. Silanization of all glassware with 5% dichlorodimethylsilane in chloroform increased the extraction recovery in plasma from 50 to 85% with high reproducibility. Mitoxantrone was unstable in human plasma. To maintain plasma sample integrity, each millilitre of sample should be fortified with 0.1 ml of 5% vitamin C (in citrate buffer) and kept frozen until analysis. Using this new method, the calibration curve of mitoxantrone in plasma in the range of interest (1-500 ng/ml) showed good linearity (r = 0.996) and precision (both between-day and within-day coefficients of variation less than 10%). The lower detection limit of this assay method was 1 ng. The application of this method allowed us to study the stability of mitoxantrone in plasma, and the pharmacokinetics of mitoxantrone in nasopharyngeal carcinoma patients receiving 12 mg/m2. The study revealed a prolonged terminal phase half-life for mitoxantrone. © 1990.
引用
收藏
页码:337 / 350
页数:14
相关论文
共 22 条
[1]   PHASE-I CLINICAL-TRIAL OF MITOXANTRONE - A NEW ANTHRACENEDIONE ANTI-CANCER DRUG [J].
ALBERTS, DS ;
GRIFFITH, KS ;
GOODMAN, GE ;
HERMAN, TS ;
MURRAY, E .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1980, 5 (01) :11-15
[2]  
BOWDEN GT, 1985, CANCER RES, V45, P4915
[3]   HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC ASSAY FOR MITOXANTRONE IN PLASMA USING ELECTROCHEMICAL DETECTION [J].
CHOI, KE ;
SINKULE, JA ;
HAN, DS ;
MCGRATH, SC ;
DALY, KM ;
LARSON, RA .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1987, 420 (01) :81-88
[4]  
CROSSLEY RJ, 1984, SEMIN ONCOL, V11, P54
[5]   MITOXANTRON DETERMINATION USING HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY - IMPROVED SENSITIVITY BY LOOP-COLUMN INJECTION FOR DUAL-DOSE PHARMACOKINETIC STUDIES [J].
CZEJKA, MJ ;
GEORGOPOULOS, A .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1988, 425 (02) :429-434
[6]   DETECTION AND SEPARATION OF MITOXANTRONE AND ITS METABOLITES IN PLASMA AND URINE BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
EHNINGER, G ;
PROKSCH, B ;
SCHILLER, E .
JOURNAL OF CHROMATOGRAPHY, 1985, 342 (01) :119-127
[7]  
FUJIMOTO S, 1982, CANCER CHEMOTH PHARM, V8, P157
[8]  
GRANT ER, 1955, J AM PHARM ASS SC ED, V44, P515
[9]  
JOHNSON RK, 1979, CANCER TREAT REP, V63, P425
[10]  
KOLLER J, 1988, CLIN PHARM, V7, P574