High-performance liquid chromatographic separation of the biotransformation products of oxaliplatin

被引:51
作者
Luo, FR
Yen, TY
Wyrick, SD
Chaney, SG [1 ]
机构
[1] Univ N Carolina, Dept Biochem & Biophys, Curriculum Toxicol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Sch Publ Hlth, Dept Environm Sci & Engn, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Sch Pharm, Div Med Chem & Nat Prod, Chapel Hill, NC 27599 USA
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 1999年 / 724卷 / 02期
关键词
oxaliplatin;
D O I
10.1016/S0378-4347(98)00565-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A novel single reversed-phase HPLC system was developed for separating oxaliplatin and its biotransformation products formed in rat plasma. The major stable biotransformation products of oxaliplatin formed in rat plasma were identified as Pt(dach)(Cys)(2), Pt(dach)(Met) and free dach. The minor biotransformation products Pt(dach)Cl-2, Pt(dach)(GSH) and Pt(dach)(GSH), could also be resolved from other Pt-dach complexes. Among these biotransformation products, the identification of Pt(dach)(Met) was further confirmed by LC-ESI-MS, and the identification of Pt(dach)(Cys)(2) Pt(dach)(GSH), Pt(dach)(GSH)(2) and free dach was confirmed by atomic absorption and double isotope labeling. This HPLC technique should prove useful for separating and identifying the biotransformation products of Pt-dach drugs such as oxaliplatin, ormaplatin and Pt(dach)(mal) in biological fluids. This will allow a more complete characterization of the pharmacokinetics and biotransformations of these Pt-dach drugs, which should in turn lead to a better understanding of the mechanisms leading to their toxicity and efficacy. (C) 1999 Elsevier Science BN, All rights reserved.
引用
收藏
页码:345 / 356
页数:12
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