School of Pharmacy, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong Special Administrative Region.
J Pharm Biomed Anal. 2012 Mar 5;61:57-63. doi: 10.1016/j.jpba.2011.11.025. Epub 2011 Dec 3.
The current study aims to investigate the pharmacokinetics and brain disposition of tacrine and its three major bioactive monohydroxylated metabolites (1-hydroxytacrine, 2-hydroxytacrine and 4-hydroxytacrine). An assay for simultaneous quantification of tacrine and three above metabolites in rat plasma and brain tissue was developed. Four analytes together with internal standard were extracted from rat plasma or brain tissue homogenate by liquid-liquid extraction using ethyl acetate. Baseline separation of the four studied compounds was achieved by a Thermo Hypersil BDS C(18) column with gradient elution using acetonitrile and ammonium formate-triethylamine (pH 4.0) under fluorescence detection. Extraction recoveries of all analytes ranged from 82.1% to 93.2% in both rat plasma and brain tissue. The intra- and inter-day precision and accuracy of each analyte at lower limit of quantification (LLOQ) and three quality control (QC) concentrations (low, middle and high) was within 12% RSD and within 11% bias in both biological matrices. The LLOQ for tacrine, 1-hydroxytacrine, 2-hydroxytacrine and 4-hydroxytacrine were found to be 2.5, 6.7, 2.1 and 2.1 ng/ml in plasma, and 12.3, 33.5, 10.6 and 10.5 ng/g in brain tissue, respectively. All four analytes were stable during analysis. The developed method provides a simple, sensitive and reproducible procedure for pharmacokinetics and brain disposition study of tacrine and its three major metabolites in rats after oral administration of tacrine. Pharmacokinetic study demonstrated that tacrine could be quickly absorbed and extensively metabolized to its monohydroxylated metabolites in vivo. In addition, rat brain disposition study showed that tacrine and its monohydroxylated metabolites were evenly distributed in different brain regions except for a slight lower concentration of tacrine in olfactory region. Moreover, tacrine and 4-hydroxytacrine exhibited a much higher brain-to-plasma ratio than that of 1-hydroxytacrine and 2-hydroxytacrine.
本研究旨在探讨他克林及其三种主要生物活性单羟基代谢物(1-羟基他克林、2-羟基他克林和 4-羟基他克林)的药代动力学和脑内分布。建立了一种同时定量检测大鼠血浆和脑组织中他克林和三种代谢物的分析方法。采用乙酸乙酯进行液-液萃取,从大鼠血浆或脑组织匀浆中提取四种分析物和内标。采用 Thermo Hypersil BDS C(18)柱,以乙腈和甲酸铵-三乙胺(pH 4.0)为流动相进行梯度洗脱,荧光检测实现四种研究化合物的基线分离。所有分析物在大鼠血浆和脑组织中的提取回收率均在 82.1%至 93.2%之间。在两种生物基质中,定量下限(LLOQ)和三个质控(QC)浓度(低、中、高)下,每种分析物的日内和日间精密度和准确度均在 12%RSD 以内,偏差在 11%以内。他克林、1-羟基他克林、2-羟基他克林和 4-羟基他克林在血浆中的 LLOQ 分别为 2.5、6.7、2.1 和 2.1ng/ml,在脑组织中的 LLOQ 分别为 12.3、33.5、10.6 和 10.5ng/g。所有四种分析物在分析过程中均稳定。该方法为他克林及其三种主要代谢物在大鼠口服给药后的药代动力学和脑内分布研究提供了一种简单、灵敏、重现性好的方法。药代动力学研究表明,他克林在体内可迅速吸收并广泛代谢为其单羟基代谢物。此外,大鼠脑内分布研究表明,他克林及其单羟基代谢物在不同脑区均匀分布,除嗅区他克林浓度稍低外。此外,他克林和 4-羟基他克林的脑/血浆比值明显高于 1-羟基他克林和 2-羟基他克林。