High throughput assay for the determination of lumefantrine in plasma

被引:44
作者
Annerberg, A
Singtoroj, T
Tipmanee, P
White, NJ
Day, NPJ
Lindegårdh, N
机构
[1] Mahidol Univ, Fac Trop Med, Wellcome Unit, Bangkok 10400, Thailand
[2] Univ Oxford, Ctr Trop Med, Nuffield Dept Clin Med, Oxford, England
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2005年 / 822卷 / 1-2期
基金
英国惠康基金;
关键词
antimalarial; high throughput; liquid chromatography; lumefantrine; solid phase extraction; 96-well;
D O I
10.1016/j.jchromb.2005.06.022
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A high throughput bioanalytical assay for the determination of lumefantrine in plasma has been developed and validated extensively. The within-day precisions for lumefantrine were 5.2, 3.5 and 2.5% at 200, 2000 and 15000 ng/mL, respectively. The between-day precisions were 4.0, 2.8 and 3.1 % at 200, 2000 and 15000 ng/mL, respectively. The lower limits of quantification (LLOQ) and the limits of detection (LOD) were 25 and 10 ng/mL, respectively using 0.250 mL plasma. The average recovery of lumefantrine was 85% and independent upon concentration. The use of 96-well plate format and short chromatographic run has increased the daily sample throughput four times. The assay is particularly suitable for large therapeutic drug monitoring studies using day 7 sampling. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:330 / 333
页数:4
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