Simultaneous monitoring of argatroban and its major metabolite using an HPLC method: Potential clinical applications

被引:18
作者
Ahmad, S
Ahsan, A
George, M
Iqbal, O
Jeske, WP
McKenna, R
Lewis, BE
Walenga, JM
Fareed, J
机构
[1] Loyola Univ, Stritch Sch Med, Dept Pathol, Maywood, IL 60153 USA
[2] Loyola Univ, Stritch Sch Med, Dept Pharmacol, Maywood, IL 60153 USA
[3] Loyola Univ, Stritch Sch Med, Cardiovasc Inst, Maywood, IL 60153 USA
关键词
argatroban; M1-metabolite; HPLC; antithrombin drugs; heparin-induced thrombocytopenia;
D O I
10.1177/107602969900500409
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Argatroban is a peptidomimetic inhibitor of thrombin that is currently undergoing extensive clinical trials as a heparin substitute for thrombotic complications. Argatroban is readily metabolized into a major derivative, MI, that has pharmacological characteristics distinct from its parent compound. The currently available clot-based assays measure the cumulative anticoagulant effect of argatroban and its metabolite(s). Available HPLC methods do not differentiate between argatroban and MI-metabolite. A modified method was developed to simultaneously quantitate MI-metabolite and argatroban in biological fluids. Initial validation studies for the method included clinical trials of argatroban in patients with heparin-induced thrombocytopenia, (ARC 911 Study) and coronary interventional procedures (ARG 310 Study). Plasma samples were extracted with acetonitrile and reconstituted in a mobile phase. Calibration curves were prepared by running known standards of: argatroban and MI-metabolite in normal human plasma. Ultraviolet detection was made at 320 nm. The retention times for argatroban and MI-metabolite peaks were found to be 10.5 +/- 0.3 minutes and 3.9 +/- 0.1 minutes, respectively. The extraction efficiency was > 95% (r(2) = 0.99). In heparin-induced thrombocytopenia patients with major bleeding complications (n = 30), the relative increase in M1-metabolite compared to argatroban varied widely (two- to eight-fold). The mean concentration of argatroban during the steady infusion period was found to be 0.7 +/- 0.35 mu g/mL, and for M1-metabolite, it was 5.5 +/- 2.8 mu g/mL. Proportionate results were not seen when higher dosages of argatroban were administered (coronary angioplasty studies). Argatroban and M1-metabolite levels also compared well with the results in global clotting assays. Owing to the simultaneous quantitation of argatroban and Mi-metabolite, this method provides a rapid assessment of the pharmacokinetics and pharmacodynamics of argatroban. The differential quantitation may be useful in the assessment of relative metabolic turnover of argatroban that can be related to the hepatic and renal functions in a given patient.
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页码:252 / 258
页数:7
相关论文
共 15 条
[1]   Pharmacokinetics and pharmacodynamics of argatroban as studied by HPLC and functional methods: Implications in the monitoring and dosage-optimizations in cardiovascular patients [J].
Ahmad, S ;
Ahsan, A ;
Iqbal, O ;
Hoppensteadt, DA ;
Lewis, BE ;
Walenga, JM ;
Fareed, J .
CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, 1998, 4 (04) :243-249
[2]  
AHMAD S, 1999, ANN HEMATOL, V78, pA67
[3]  
BANNER DW, 1991, J BIOL CHEM, V266, P20085
[4]  
BERRY CN, 1994, THROMB HAEMOSTASIS, V72, P381
[5]   COMPARATIVE-STUDIES ON THE ANTICOAGULANT AND PROTEASE GENERATION INHIBITORY ACTIONS OF NEWLY DEVELOPED SITE-DIRECTED THROMBIN INHIBITORY DRUGS - EFEGATRAN(R), ARGATROBAN, HIRULOG, AND HIRUDIN [J].
CALLAS, DD ;
HOPPENSTEADT, D ;
FAREED, J .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 1995, 21 (02) :177-183
[6]   COMBINED ADMINISTRATION OF ASPIRIN AND A SPECIFIC THROMBIN INHIBITOR IN MAN [J].
CLARKE, RJ ;
MAYO, G ;
FITZGERALD, GA ;
FITZGERALD, DJ .
CIRCULATION, 1991, 83 (05) :1510-1518
[7]   Argatroban: A synthetic thrombin inhibitor of low relative molecular mass [J].
Fitzgerald, D ;
Murphy, N .
CORONARY ARTERY DISEASE, 1996, 7 (06) :455-458
[8]   A randomized, blinded study of two doses of Novastan® (brand of argatroban) versus heparin as adjunctive therapy to recombinant tissue plasminogen activator (accelerated administration) in acute myocardial infarction:: Rationale and design of the myocardial infarction using Novastan® and t-PA (MINT) study [J].
Jang, IK ;
Giugliano, RP ;
Massey, TJ ;
Schwarz, RP .
JOURNAL OF THROMBOSIS AND THROMBOLYSIS, 1998, 5 (01) :49-52
[9]  
Jeske W, 1999, Expert Opin Investig Drugs, V8, P625
[10]   Anticoagulation with Novastan® (argatroban) in patients with heparin-induced thrombocytopenia and heparin-induced thrombocytopenia and thrombosis syndrome [J].
Lewis, BE ;
Walenga, JM ;
Wallis, DE .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 1997, 23 (02) :197-202