Method development and validation of a high-performance liquid chromatographic method for tramadol in human plasma using liquid-liquid extraction

被引:74
作者
Gan, SH [1 ]
Ismail, R
Adnan, WAW
Wan, Z
机构
[1] Univ Sains Malaysia, Sch Med Sci, Dept Pharmacol, Kubang Kerian 16150, Kelantan, Malaysia
[2] Univ Sains Malaysia, Sch Med Sci, Dept Anaesthesiol, Kubang Kerian 16150, Kelantan, Malaysia
[3] Univ Sains Malaysia, Sch Med Sci, Dept Orthopaed, Kubang Kerian 16150, Kelantan, Malaysia
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2002年 / 772卷 / 01期
关键词
tramadol;
D O I
10.1016/S1570-0232(02)00065-X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An HPLC system using a simple liquid-liquid extraction and HPLC with UV detection has been validated to determine tramadol concentration in human plasma. The method developed was selective and linear for concentrations ranging from 10 to 2000 ng/ml with average recovery of 98.63%. The limit of quantitation (LOQ) was 10 ng/ml and the percentage recovery of the internal standard phenacetin was 76.51%. The intra-day accuracy ranged from 87.55 to 105.99% and the inter-day accuracy, 93.44 to 98.43% for tramadol. Good precision (5.32 and 6.67% for intra- and inter-day, respectively) was obtained at LOQ. The method has been applied to determine tramadol concentrations in human plasma samples for a pharmacokinetic study. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:123 / 129
页数:7
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