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基质辅助激光解吸电离飞行时间质谱法联用喹诺酮基质添加剂定量检测人血浆中的喹那普利。

Quantitation of quinapril in human plasma by matrix-assisted laser desorption ionization time-of-flight mass spectrometry with quinolone matrix additives.

机构信息

Department of Biochemistry, College of Medicine, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Sep 15;879(26):2688-94. doi: 10.1016/j.jchromb.2011.07.026. Epub 2011 Aug 7.

DOI:10.1016/j.jchromb.2011.07.026
PMID:21868293
Abstract

The renin-angiotensin-aldosterone system (RAAS) is an essential body fluid maintenance system that controls pressure in the human body. The conversion of angiotensin I to angiotensin II by angiotensin-converting enzyme (ACE) is a key process in the RAAS because angiotensin II causes the vasoconstriction association with hypertension. Because of its effectiveness as an ACE blocker, quinipril is widely used for clinical treatment of hypertension and chronic congestive heart failure(.) Matrix-assisted laser desorption/ionization coupled with time-of-flight analyzer (MALDI-TOF) is a high throughput instrument for biological sample analysis. This study developed a micro-scale approach for using MALDI-TOF to detect quinapril in biological samples. A micro-liquid-liquid-extraction strategy combined with ion-pair interaction successfully extracted quinapril from aqueous layer to organic layer. Quinolones were then used as matrix additives to suppress undesired substances in plasma produce signals. Several factors affecting extraction efficiency were investigated in a biosample with a volume of only 10 μL. This method is successful to monitor quinapril in the clinical therapeutic range. The proposed method proved effective for monitoring the trace amounts of quinapril typically used for clinical therapy. The relative standard deviation (R.S.D.) and relative error (R.E.) used for evaluating within- and between-day assays of quinapril in plasma consistently remained below 15%.

摘要

肾素-血管紧张素-醛固酮系统(RAAS)是一个重要的体液维持系统,它控制着人体的血压。血管紧张素转换酶(ACE)将血管紧张素 I 转化为血管紧张素 II 是 RAAS 的一个关键过程,因为血管紧张素 II 会导致与高血压相关的血管收缩。由于喹那普利作为 ACE 抑制剂的有效性,它被广泛用于临床治疗高血压和慢性充血性心力衰竭。基质辅助激光解吸/电离与飞行时间分析(MALDI-TOF)是一种高通量的生物样本分析仪器。本研究开发了一种微尺度方法,使用 MALDI-TOF 检测生物样本中的喹那普利。一种微液-液萃取策略与离子对相互作用相结合,成功地将喹那普利从水层提取到有机层。然后,喹诺酮类物质被用作基质添加剂,以抑制等离子体中产生信号的不需要的物质。在只有 10 μL 体积的生物样本中研究了影响萃取效率的几个因素。该方法成功地监测了临床治疗范围内的喹那普利。该方法可用于监测临床治疗中常用的痕量喹那普利。用于评估血浆中喹那普利的日内和日间测定的相对标准偏差(RSD)和相对误差(RE)始终保持在 15%以下。

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