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首页> 外文期刊>International journal of analytical chemistry >Determination of Chlorpromazine, Haloperidol, Levomepromazine, Olanzapine, Risperidone, and Sulpiride in Human Plasma by Liquid Chromatography/Tandem Mass Spectrometry (LC-MS/MS)
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Determination of Chlorpromazine, Haloperidol, Levomepromazine, Olanzapine, Risperidone, and Sulpiride in Human Plasma by Liquid Chromatography/Tandem Mass Spectrometry (LC-MS/MS)

机译:液相色谱/串联质谱法(LC-MS / MS)测定人血浆中的氯丙嗪,氟哌啶醇,左旋丙嗪,奥氮平,利培酮和舒必利

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Background and Objective. In this study, turbo-ion spray as an interface of tandem mass spectrometry (MS/MS) was performed for sensitive and accurate quantification of chlorpromazine, haloperidol, levomepromazine, olanzapine, risperidone, and sulpiride in plasma samples. Methods. Separation was performed by gradient reversed phase high-performance liquid chromatography using a mobile phase containing ammonium formiate 2 mM, pH 2.7, and acetonitrile flowing through a Restek PFP Propyl C18 analytical column (50 mm×2.1 mm i.d.) with particle size of 5 µm, at a flow rate of 800 µL/min. Positive ion fragments were detected in multiple reaction monitoring (MRM) mode. Sample preparation was achieved by solid phase extraction (SPE) (Oasis HLB). Results. Mean extraction recoveries ranged from 82.75% to 100.96%. The standard calibration curves showed an excellent linearity, covering subtherapeutic, therapeutic, and toxic ranges. Intraday and interday validation using quality control (QC) samples were performed. The inaccuracy and imprecision were below 12% at all concentration levels. The limits of detection (LOD) and quantification (LOQ) for all analytes were under therapeutic ranges for all tested analytes. Thus, the proposed method was sensitive enough for the detection and determination of subtherapeutic levels of these antipsychotics in plasma samples. No interference of endogenous or exogenous molecules was observed and no carryover effects were recorded. Conclusion. According to the results, the proposed method is simple, specific, linear, accurate, and precise and can be applied for antipsychotic analysis in clinical routine. This method was applied for the determination of the tested antipsychotics in plasma samples taken from 71 individuals.
机译:背景和目标。在这项研究中,采用涡轮离子喷雾作为串联质谱(MS / MS)的接口,可对血浆样品中的氯丙嗪,氟哌啶醇,左丙丙嗪,奥氮平,利培酮和舒必利进行灵敏而准确的定量。方法。通过梯度反相高效液相色谱法进行分离,其中使用的流动相中含有2 mM甲酸铵,pH 2.7和乙腈,流经Restek PFP Propyl C18分析柱(内径50 mm×2.1 mm),粒径为5 µm。 ,流速为800 µL / min。在多反应监测(MRM)模式下检测到正离子碎片。样品制备通过固相萃取(SPE)(Oasis HLB)实现。结果。平均提取回收率在82.75%至100.96%之间。标准校准曲线显示出极好的线性,涵盖亚治疗,治疗和毒性范围。使用质量控制(QC)样品进行日内和日间验证。在所有浓度水平下,误差和不精确度均低于12%。所有分析物的检出限(LOD)和定量限(LOQ)均在所有被测分析物的治疗范围内。因此,所提出的方法对于检测和确定血浆样品中这些抗精神病药的亚治疗水平足够灵敏。没有观察到内源性或外源性分子的干扰,也没有记录到残留效应。结论。结果表明,该方法简单,特异,线性,准确,准确,可用于临床常规抗精神病分析。该方法用于测定从71名个体中提取的血浆样品中的抗精神病药。

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