首页> 美国卫生研究院文献>Molecules >Butyl Methacrylate-Co-Ethylene Glycol Dimethacrylate Monolith for Online in-Tube SPME-UHPLC-MS/MS to Determine Chlopromazine Clozapine Quetiapine Olanzapine and Their Metabolites in Plasma Samples
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Butyl Methacrylate-Co-Ethylene Glycol Dimethacrylate Monolith for Online in-Tube SPME-UHPLC-MS/MS to Determine Chlopromazine Clozapine Quetiapine Olanzapine and Their Metabolites in Plasma Samples

机译:甲基丙烯酸丁酯-乙二醇二甲基丙烯酸乙二醇酯在线管内SPME-UHPLC-MS / MS测定血浆样品中的氯丙嗪氯氮平喹硫平奥氮平及其代谢物

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摘要

This manuscript describes a sensitive, selective, and online in-tube solid-phase microextraction coupled with an ultrahigh performance liquid chromatography-tandem mass spectrometry (in-tube SPME-UHPLC-MS/MS) method to determine chlopromazine, clozapine, quetiapine, olanzapine, and their metabolites in plasma samples from schizophrenic patients. Organic poly(butyl methacrylate-co-ethylene glycol dimethacrylate) monolith was synthesized on the internal surface of a fused silica capillary (covalent bonds) for in-tube SPME. Analyte extraction and analysis was conducted by connecting the monolithic capillary to an UHPLC-MS/MS system. The monolith was characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectrometry (FTIR). The developed method presented adequate linearity for all the target antipsychotics: R2 was higher than 0.9975, lack-of-fit ranged from 0.115 to 0.955, precision had variation coefficients lower than 14.2%, and accuracy had relative standard error values ranging from −13.5% to 14.6%, with the exception of the lower limit of quantification (LLOQ). The LLOQ values in plasma samples were 10 ng mL−1 for all analytes. The developed method was successfully applied to determine antipsychotics and their metabolites in plasma samples from schizophrenic patients.
机译:该手稿描述了一种灵敏,选择性的在线在线固相微萃取结合超高效液相色谱-串联质谱分析法(管内SPME-UHPLC-MS / MS),用于测定氯丙嗪,氯氮平,喹硫平,奥氮平的方法,及其在精神分裂症患者血浆样品中的代谢产物。在管内SPME的熔融石英毛细管(共价键)的内表面上合成了有机聚(甲基丙烯酸丁酯-乙二醇二甲基丙烯酸乙酯)整体。通过将整体毛细管连接到UHPLC-MS / MS系统进行分析物提取和分析。通过扫描电子显微镜(SEM)和傅里叶变换红外光谱(FTIR)对整料进行表征。所开发的方法对所有目标抗精神病药均具有足够的线性:R 2 高于0.9975,失配度在0.115至0.955之间,精密度的变异系数低于14.2%,准确度相对标准误差值介于-13.5%至14.6%之间,但定量下限(LLOQ)除外。所有分析物的血浆样品中的LLOQ值为10 ng mL -1 。所开发的方法已成功地用于测定精神分裂症患者血浆中的抗精神病药及其代谢物。

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