首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Quantification of typical antipsychotics in human plasma by ultra-high performance liquid chromatography tandem mass spectrometry for therapeutic drug monitoring
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Quantification of typical antipsychotics in human plasma by ultra-high performance liquid chromatography tandem mass spectrometry for therapeutic drug monitoring

机译:超高效液相色谱串联质谱法定量检测人血浆中的典型抗精神病药,用于治疗药物监测

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A selective and sensitive method was developed for the simultaneous quantification of seven typical antipsychotic drugs (cis-chlorprothixene, flupentixol, haloperidol, levomepromazine, pipamperone, promazine and zuclopenthixol) in human plasma. Ultra-high performance liquid chromatography (UHPLC) was used for complete separation of the compounds in less than 4.5. min on an Acquity UPLC BEH C18 column (2.1. mm. ×. 50. mm; 1.7. μm), with a gradient elution of ammonium formate buffer pH 4.0 and acetonitrile at a flow rate of 400. μl/min. Detection was performed on a tandem quadrupole mass spectrometer (MS/MS) equipped with an electrospray ionization interface. A simple protein precipitation procedure with acetonitrile was used for sample preparation. Thanks to the use of stable isotope-labeled internal standards for all analytes, internal standard-normalized matrix effects were in the range of 92-108%. The method was fully validated to cover large concentration ranges of 0.2-90. ng/ml for haloperidol, 0.5-90. ng/ml for flupentixol, 1-450. ng/ml for levomepromazine, promazine and zuclopenthixol and 2-900. ng/ml for cis-chlorprothixene and pipamperone. Trueness (89.1-114.8%), repeatability (1.8-9.9%), intermediate precision (1.9-16.3%) and accuracy profiles (<30%) were in accordance with the latest international recommendations. The method was successfully used in our laboratory for routine quantification of more than 500 patient plasma samples for therapeutic drug monitoring. To the best of our knowledge, this is the first UHPLC-MS/MS method for the quantification of the studied drugs with a sample preparation based on protein precipitation.
机译:开发了一种选择性和灵敏的方法,用于同时定量测定人血浆中的七种典型的抗精神病药物(顺氯丙氧噻吩,氟喷噻醇,氟哌啶醇,左氧丙嗪,哌帕酮,丙嗪和zuclopenthixol)。使用超高效液相色谱法(UHPLC)在小于4.5的条件下完全分离化合物。在Acquity UPLC BEH C18色谱柱(2.1。mm。×。50. mm; 1.7。μm)上进行分样,以400.μl/ min的流速梯度洗脱甲酸铵缓冲液pH 4.0和乙腈。在配备有电喷雾电离接口的串联四极杆质谱仪(MS / MS)上进行检测。使用乙腈的简单蛋白质沉淀程序用于样品制备。由于对所有分析物使用了稳定的同位素标记的内标,内标归一化的基质效应在92%到88%之间。该方法经过充分验证,可以覆盖0.2-90的较大浓度范围。氟哌啶醇为ng / ml,0.5-90。 ng / ml氟喷托醇,1-450。左丙嗪,丙嗪和zuclopenthixol和2-900 ng / ml。 ng / ml表示顺式氯噻吨和哌潘酮。真实性(89.1-114.8%),可重复性(1.8-9.9%),中间精度(1.9-16.3%)和精度曲线(<30%)符合最新的国际建议。该方法已在我们的实验室中成功用于500例患者血浆样品的常规定量,以进行治疗药物监测。据我们所知,这是第一个UHPLC-MS / MS方法,用于基于蛋白质沉淀的样品制备方法对所研究药物进行定量。

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