Investigation of an anti-activated factor X (anti-Xa) assay for the quantification of enoxaparin in human plasma

被引:8
作者
Al-Sallami, Hesham S. [1 ]
Medlicott, Natalie J. [1 ]
机构
[1] Univ Otago, Sch Pharm, Dunedin 9054, New Zealand
关键词
anti-Xa; chromogenic; dalteparin; enoxaparin; haemolysis;
D O I
10.1111/jphp.12333
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
ObjectivesEnoxaparin is a low-molecular weight heparin (LMWH) widely used for the treatment of thrombosis and measured through a chromogenic assay (anti-Xa). The aim of this project was to investigate the impact of patient and sampling sources of variation on an anti-Xa assay for enoxaparin. MethodsCOATEST was used in accordance with manufacturer's instructions. A standard curve of LMWH concentration (0.1-1.0IU/ml) was prepared. The shelf-life and freeze-thaw stability of Xa over a 6-month period were investigated. The effects of blood sample haemolysis and plasma antithrombin-III (AT) concentration were examined. Key findingsThe standard curve performed well with high accuracy (average bias of 8.1%) and precision (average CV of 2.8%). The shelf-life of Xa once reconstituted could be extended from 1 month to 4 months if aliquots were frozen at -20 degrees C. Some loss of anti-Xa activity was observed on freeze-thawing (bias up to 25%). Haemolysis of 2.5% was found to interfere with the assay. AT level as low as 50% did not affect assay accuracy. ConclusionsXa standards when frozen immediately after reconstitution could be used for the following 4 months. Haemolysis interferes with the assay, but a 50% reduction in AT does not significantly affect the assay result.
引用
收藏
页码:209 / 214
页数:6
相关论文
共 11 条
[1]   Routine Plasma Anti-Xa Monitoring is Required for Low-Molecular-Weight Heparins [J].
Al-Sallami, Hesham S. ;
Barras, Michael A. ;
Green, Bruce ;
Duffull, Stephen B. .
CLINICAL PHARMACOKINETICS, 2010, 49 (09) :567-571
[2]   The Reduced Anticoagulant Effect of Fondaparinux at Low Antithrombin Levels [J].
Dempfle, Carl-Erik ;
Eichner, Julia ;
Suvajac, Nenad ;
Ahmad-Nejad, Parviz ;
Neumaier, Michael ;
Borggrefe, Martin .
ANESTHESIA AND ANALGESIA, 2009, 109 (03) :712-716
[3]  
Frydman A, 1996, HAEMOSTASIS, V26, P24
[4]   Dosing strategy for enoxaparin in patients with renal impairment presenting with acute coronary syndromes [J].
Green, B ;
Greenwood, M ;
Saltissi, D ;
Westhuyzen, J ;
Kluver, L ;
Rowell, J ;
Atherton, J .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2005, 59 (03) :281-290
[5]   Heparin and low-molecular-weight heparin - Mechanisms of action, pharmacokinetics, dosing considerations, monitoring, efficacy, and safety [J].
Hirsh, J ;
Warkentin, TE ;
Raschke, R ;
Granger, C ;
Ohman, EM ;
Dalen, JE .
CHEST, 1998, 114 (05) :489S-510S
[6]  
KOOPMANS LH, 1964, BIOMETRIKA, V51, P25, DOI 10.2307/2334192
[7]  
Sanofi-Aventis New Zealand Ltd, 2013, CLEX CLEX FORT DAT S
[8]   A general best-fit method for concentration-response curves and the estimation of low-effect concentrations [J].
Scholze, M ;
Boedeker, W ;
Faust, M ;
Backhaus, T ;
Altenburger, R ;
Grimme, LH .
ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY, 2001, 20 (02) :448-457
[9]   EVALUATION OF AN AMIDOLYTIC HEPARIN ASSAY METHOD - INCREASED SENSITIVITY BY ADDING PURIFIED ANTITHROMBIN-III [J].
TEIEN, AN ;
LIE, M .
THROMBOSIS RESEARCH, 1977, 10 (03) :399-410
[10]  
Watson DG, 2005, PHARM ANAL TXB PHRAM