Pitfalls in monitoring tacrolimus (FK 506)

被引:17
作者
Braun, F
Schutz, E
Christians, U
Lorf, T
Schiffmann, JH
Armstrong, VW
Schroter, W
Sewing, KF
Oellerich, M
Ringe, B
机构
[1] UNIV GOTTINGEN, KLIN TRANSPLANTAT CHIRURG, D-37075 GOTTINGEN, GERMANY
[2] UNIV GOTTINGEN, KLIN CHEM ABT, D-37075 GOTTINGEN, GERMANY
[3] UNIV GOTTINGEN, ABT KINDERHEILKUNDE, D-37075 GOTTINGEN, GERMANY
[4] HANNOVER MED SCH, INST ALLGEMEINE PHARMAKOL, HANNOVER, GERMANY
关键词
therapeutic drug monitoring; tacrolimus; liver transplantation;
D O I
10.1097/00007691-199712000-00004
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Tacrolimus (FK 506) is a new, potent immunosuppressive drug for primary and rescue therapy in liver and kidney transplantation. Therapeutic drug monitoring is essential for this drug because of its narrow therapeutic window. Blood levels are monitored routinely by enzyme linked immunoassay (ELISA) or by microparticle enzyme immunoassay (MEIA). In a 13-year-old recipient of a liver transplant who had poor hepatic function during: the first postoperative week, the authors observed unusually high tacrolimus blood concentrations using either the ELISA (26.6 to 49.0 mu g/l) or MEIA (58.5 to 64.5 mu g/l). Parent drug levels measured in the same blood samples by high-performance Liquid chromatography/mass spectrometry (HPLC/MS) were up to 10-fold lower (5.1 to 9.0 mu g/l). The discrepancies between the immunoassay and HPLC/MS results could not be attributed to any of the known metabolites of tacrolimus.
引用
收藏
页码:628 / 631
页数:4
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