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使用二维柱切换的高效液相色谱法直接分析血浆中的多巴胺激动剂(-)-2-(N-丙基-N-2-噻吩基乙氨基)-5-羟基四氢萘盐酸盐。

Direct analysis of the dopamine agonist (-)-2-(N-propyl-N-2-thienylethylamino)-5-hydroxytetralin hydrochloride in plasma by high-performance liquid chromatography using two-dimensional column switching.

作者信息

Ruckmick S C, Hench B D

机构信息

Whitby Research, Inc., Irvine, CA 92715.

出版信息

J Chromatogr. 1991 Apr 19;565(1-2):277-95. doi: 10.1016/0378-4347(91)80390-x.

DOI:10.1016/0378-4347(91)80390-x
PMID:1678747
Abstract

A reversed-phase, two-dimensional, liquid chromatographic method incorporating column switching and electrochemical detection was used for the direct analysis of the dopamine (D2) agonist (-)-2-(N-propyl-N-2-thienylethylamino)-5-hydroxytetralin hydrochloride in plasma. Sample work-up consisted of addition of internal standard, filtration, then direct injection of the plasma sample onto an internal surface reversed-phase (ISRP) guard column where the dopamine agonist and internal standard were separated from plasma proteins. An automated pneumatic valve was then used to switch to a stronger eluent which stripped the retained substances from the ISRP support onto a C18 analytical column where the analytes were separated from endogenous biological interferences. A dual-electrode electrochemical detector was used to minimize interferences and provide the desired sensitivity. The method has a detection limit of 1.5 ng/ml and requires a total assay time of 20 min per plasma sample. The method is linear from 1.5 to 1000 ng/ml and yielded greater than 80% drug recovery for plasma concentrations greater than 10 ng/ml. Precision for the method at 100 ng/ml yielded a relative standard deviation of 4.4%. Reproducibility was within 6.5% on a 20 ng/ml spiked plasma sample assayed on different days by different people. The method has successfully been applied to human plasma samples and for pharmacokinetic studies in rats and monkeys.

摘要

采用一种结合柱切换和电化学检测的反相二维液相色谱法,直接分析血浆中的多巴胺(D2)激动剂盐酸(-)-2-(N-丙基-N-2-噻吩基乙氨基)-5-羟基四氢萘。样品处理包括加入内标、过滤,然后将血浆样品直接进样到内表面反相(ISRP)保护柱上,多巴胺激动剂和内标在此与血浆蛋白分离。接着使用自动气动阀切换到更强的洗脱液,将保留在ISRP载体上的物质洗脱到C18分析柱上,在此分析物与内源性生物干扰物分离。使用双电极电化学检测器以尽量减少干扰并提供所需的灵敏度。该方法的检测限为1.5 ng/ml,每个血浆样品的总分析时间为20分钟。该方法在1.5至1000 ng/ml范围内呈线性,对于血浆浓度大于10 ng/ml的情况,药物回收率大于80%。该方法在100 ng/ml时的精密度,相对标准偏差为4.4%。在不同日期由不同人员对加标20 ng/ml血浆样品进行分析时,重现性在6.5%以内。该方法已成功应用于人体血浆样品以及大鼠和猴子的药代动力学研究。

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