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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:用超高效液相色谱串联质谱法定量人血浆中典型抗精神病药物治疗药物监测

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摘要

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敏感方法,用于同时定量七种典型的抗精神病药物(CIS-氯化替烯,Flupentixol,氟哌啶醇,Levomepromazine,普氏蛋白,普氏蛋白酶和Zuclopenthixol)。超高效液相色谱(UHPLC)用于在小于4.5的含量小于4.5时完全分离化合物。 Acquity UPLC BEH C18列(2.1.mm。×50. mm;1.7μm)。以400μl/ min的流速,铵甲酸铵pH 4.0和乙腈的梯度洗脱。在配备有电喷雾电离界面的串联四极谱质谱仪(MS / MS)上进行检测。使用乙腈的简单蛋白质沉淀方法用于样品制备。由于使用稳定的同位素标记的所有分析物的内标,内部标准标准化的基质效应在92-108%的范围内。该方法完全验证以覆盖大浓度范围为0.2-90。 Ng / ml对于氟哌啶醇,0.5-90。 Flupentixol,1-450的Ng / ml。 Ng / ml对于Levomepromazine,Promazine和Zuclopenthixol和2-900。 Ng / ml用于CIS-氯丙二醇和磷酸盐。真实的(89.1-114.8%),可重复性(1.8-9.9%),中间精度(1.9-16.3%)和准确性概况(<30%)符合最新的国际建议。该方法在我们的实验室中成功地用于常规定量超过500例患者血浆样品进行治疗药物监测。据我们所知,这是第一批UHPLC-MS / MS方法,用于定量所研究的药物,基于蛋白质沉淀的样品制备。

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