Liquid chromatography-tandem mass spectrometry determination of baclofen in various biological samples and application to a pharmacokinetic study

被引:16
作者
Kim, Tae Hwan [1 ]
Shin, Soyoung [2 ]
Shin, Jeong Cheol [3 ]
Choi, Jin Ho [3 ]
Seo, Won Sik [3 ]
Park, Gi-Young [4 ]
Kwon, Dong Rak [4 ]
Yoo, Sun Dong [1 ]
Lee, Ah-Ram [1 ]
Joo, Sang Hoon [3 ]
Min, Byung Sun [3 ]
Yoo, Won Young [1 ]
Shin, Beom Soo [3 ]
机构
[1] Sungkyunkwan Univ, Sch Pharm, Suwon, Gyeonggi D, South Korea
[2] Wonkwang Univ, Coll Pharm, Iksan, Jeonbuk, South Korea
[3] Catholic Univ Daegu, Coll Pharm, Gyongsan 712702, Gyeongbuk, South Korea
[4] Catholic Univ Daegu, Sch Med, Dept Rehabil Med, Taegu, South Korea
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2013年 / 938卷
基金
新加坡国家研究基金会;
关键词
Baclofen; LC/MS/MS; Pharmacokinetics; Tissue distribution; RECEPTOR AGONIST BACLOFEN; SOLID-PHASE EXTRACTION; ACID BACLOFEN; ARBACLOFEN PLACARBIL; CEREBROSPINAL-FLUID; HUMAN PLASMA; URINE; DERIVATIZATION; LIORESAL; EFFICACY;
D O I
10.1016/j.jchromb.2013.08.030
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Baclofen is a structural analogue of gamma-aminobutyric acid (GABA) that has been used for the treatment of spasticity since 1977. This study describes a simple and sensitive LC/MS/MS assay for the quantification of baclofen in rat plasma, urine, as well as various tissue samples. The assay utilized a simple protein precipitation and achieved lower limit of quantification (LLOQ) of 0.25 ng/mL for rat plasma and brain samples and 2 ng/mL for rat urine, liver and kidney samples. The assay was validated to demonstrate the specificity, linearity, recovery, LLOQ accuracy, precision, and stability by using matrix matched quality control samples. There is no endogenous or exogenous peaks interfering with the analytes and matrix effects were minimized by optimized separation condition. The assay was linear over a concentration range of 0.25-500 ng/mL for rat plasma and brain tissue, and 2-5000 ng/mL for rat urine, kidney and liver with correlation coefficients >0.999. The mean intra- and inter-day assay accuracies were 94.6-104.6 and 96.0-103.6%, respectively. The mean intra- and inter-day precisions were 5.71 and 5.70%, respectively. The developed assay was successfully applied to a pharmacokinetic study and examined urinary excretion and tissue distribution of baclofen in rats following intravenous and oral administration. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:43 / 50
页数:8
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