H-1-NMR STUDIES OF HUMAN URINE - URINARY ELIMINATION OF THE ANTICANCER DRUG CARBOPLATIN

被引:13
作者
RANFORD, JD
SADLER, PJ
BALMANNO, K
NEWELL, DR
机构
[1] UNIV LONDON,BIRKBECK COLL,DEPT CHEM,GORDON HOUSE,29 GORDON SQ,LONDON WC1H 0PP,ENGLAND
[2] UNIV NEWCASTLE UPON TYNE,SCH MED,CANC RES UNIT,NEWCASTLE NE2 4HH,ENGLAND
关键词
H-1; NMR; URINE; METABOLITES; PLATINUM ANTICANCER DRUG; CARBOPLATIN; PARAPLATIN; CBDCA;
D O I
10.1002/mrc.1260291321
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Samples of urine from a patient obtained before and after treatment with 300 mg of the anticancer drug [Pt(II)(NH3)2(CBDCA)] (carboplatin, "Paraplatin", where CBCDA is 1,1-dicarboxycyclobutane) have been analysed using 500 MHz 1D and 2D H-1 NMR spectroscopy. Peaks for the intact drug and the free ligand CBDCA have been assigned and are present in a mol ratio of ca. 5:1. Only about one half of the total Pt in the sample was present as intact drug. Relative to creatinine and citrate, the excretion of hippurate increased by a factor of ca. 4 after drug treatment. This work suggests that NMR spectroscopy can play a valuable role in studies of carboplatin metabolism.
引用
收藏
页码:S125 / S129
页数:5
相关论文
共 18 条
[1]   H-1-NMR STUDIES OF URINE DURING FASTING - EXCRETION OF KETONE-BODIES AND ACETYLCARNITINE [J].
BALES, JR ;
BELL, JD ;
NICHOLSON, JK ;
SADLER, PJ .
MAGNETIC RESONANCE IN MEDICINE, 1986, 3 (06) :849-856
[2]  
BALES JR, 1984, CLIN CHEM, V30, P426
[3]  
Bell J D, 1989, NMR Biomed, V2, P246, DOI 10.1002/nbm.1940020513
[4]  
DEWAAL WAJ, 1990, J PHARM BIOMED ANAL, V8, P30
[5]  
HACKER MP, 1983, PLATINUM COORDINATIO
[6]  
HARLAND SJ, 1984, CANCER RES, V44, P1693
[7]  
ILES RA, 1985, CLIN CHEM, V31, P1795
[8]  
ISMAIL IM, 1983, ACS SYM SER, V209, P171
[9]  
MARTELL AE, 1977, CRTICAL STABILITY CO, V3, P106
[10]  
MCBRIEN CH, 1986, BIOCH MECHANISMS PLA