Development and validation of an HPLC method for the rapid and simultaneous determination of 6-mercaptopurine and four of its metabolites in plasma and red blood cells

被引:61
作者
Hawwa, Ahmed F. [1 ]
Millership, Jeff S. [1 ]
Collier, Paul S. [1 ]
McElnay, James C. [1 ]
机构
[1] Queens Univ Belfast, Ctr Med Biol, Sch Pharm, Clin & Practice Res Grp,PK PD Core Lab, Belfast BT9 7BL, Antrim, North Ireland
关键词
6-Mercaptopurine; 6-Thioguanine nucleotides; Paediatrics; Leukaemia; Inflammatory bowel disease; HPLC; THIOPURINE METHYLTRANSFERASE; 6-THIOGUANINE; NUCLEOTIDES; AZATHIOPRINE; CHILDREN; ARTICLE;
D O I
10.1016/j.jpba.2008.10.045
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An HPLC method has been developed and validated for the rapid determination of mercaptopurine and four of its metabolites; thioguanine, thiouric acid, thioxanthine and methylmercaptopurine in plasma and red blood cells. The method involves a simple treatment procedure based on deproteinisation by perchloric acid followed by acid hydrolysis and heating for 45 min at 100 degrees C. The developed method was linear over the concentration range studied with a correlation coefficient >0.994 for all compounds in both plasma and erythrocytes. The lower limits of quantification were 13, 14, 3, 2, 95 pmol/8 x 101 RBCs and 2, 5, 2, 3, 20 ng/ml plasma for thioguanine, thiouric acid, mercaptopurine, thioxanthine and methylmercaptopurine, respectively. The method described is selective and sensitive enough to analyse the different metabolites in a single run under isocratic conditions. Furthermore, it has been shown to be applicable for monitoring these metabolites in paediatric patients due to the low volume requirement (200 mu l of plasma or erythrocytes) and has been successfully applied for investigating population pharmacokinetics, pharmacogenetics and non-adherence to therapy in these patients. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:401 / 409
页数:9
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