Quantification of doxorubicin and metabolites in rat plasma and small volume tissue samples by liquid chromatography/electrospray tandem mass spectroscopy

被引:120
作者
Arnold, RD [1 ]
Slack, JE [1 ]
Straubinger, RM [1 ]
机构
[1] SUNY Buffalo, Dept Pharmaceut Sci, Amherst, NY 14260 USA
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2004年 / 808卷 / 02期
关键词
doxorubicin; anthracyclines;
D O I
10.1016/j.jchromb.2004.04.030
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The anthracycline Doxorubicin (DXR) is used widely for the treatment of human malignancies, and drug delivery technologies are under investigation to enhance antitumor selectivity and effectiveness. A liquid chromatography-tandem mass spectroscopy (LC-MS/MS) method was developed to identify and quantify DXR and key metabolites in small-volume biological samples. The assay was linear over the therapeutically relevant concentration range (0.125-10,000 nM); in brain tissue, the lower limit of quantification was 0.247 nM and the sensitivity was 1.4 pg. The ability to quantify DXR and detect metabolite formation may provide insight into the toxicity and bioavailability of drug incorporated into carriers such as liposomes. OF (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:141 / 152
页数:12
相关论文
共 36 条
[1]   High-performance liquid chromatographic validated assay of doxorubicin in rat plasma and tissues [J].
Alvarez-Cedrón, L ;
Sayalero, ML ;
Lanao, JM .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 1999, 721 (02) :271-278
[2]   A SENSITIVE AND SIMPLE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC METHOD FOR THE DETERMINATION OF DOXORUBICIN AND ITS METABOLITES IN PLASMA [J].
ANDERSEN, A ;
WARREN, DJ ;
SLORDAL, L .
THERAPEUTIC DRUG MONITORING, 1993, 15 (05) :455-461
[3]   STABILITY OF LIPOSOMAL DOXORUBICIN FORMULATIONS - PROBLEMS AND PROSPECTS [J].
BARENHOLZ, Y ;
AMSELEM, S ;
GOREN, D ;
COHEN, R ;
GELVAN, D ;
SAMUNI, A ;
GOLDEN, EB ;
GABIZON, A .
MEDICINAL RESEARCH REVIEWS, 1993, 13 (04) :449-491
[4]  
BARTLETT GR, 1959, J BIOL CHEM, V234, P466
[5]   Investigation of the enterohepatic recirculation of Adriamycin and its metabolites by a linked-rat model [J].
Behnia, K ;
Boroujerdi, M .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1998, 41 (05) :370-376
[6]  
CHAN KK, 1973, RES COMMUN CHEM PATH, V6, P447
[7]   DETERMINATION OF ADRIAMYCIN IN PLASMA AND TISSUE BIOPSIES [J].
COX, SK ;
WILKE, AV ;
FRAZIER, D .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1991, 564 (01) :322-329
[8]   Determination of doxorubicin and doxorubicinol in plasma of cancer patients by high-performance liquid chromatography [J].
de Bruijn, P ;
Verweij, J ;
Loos, WJ ;
Kolker, HJ ;
Planting, AST ;
Nooter, K ;
Stoter, G ;
Sparreboom, A .
ANALYTICAL BIOCHEMISTRY, 1999, 266 (02) :216-221
[9]  
DEVITA VT, 2001, CANC PRINCPILES PRAC
[10]  
DIMARCO A, 1969, CANCER CHEMOTH REP 1, V53, P33