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 >Sensitive determination of a pharmaceutical compound and its metabolites in human plasma by ultra-high performance liquid chromatography-tandem mass spectrometry with on-line solid-phase extraction.
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Sensitive determination of a pharmaceutical compound and its metabolites in human plasma by ultra-high performance liquid chromatography-tandem mass spectrometry with on-line solid-phase extraction.

机译:在线固相萃取超高效液相色谱-串联质谱法灵敏测定人血浆中的药物化合物及其代谢物。

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This paper describes the determination of a drug candidate and two metabolites in human plasma by column-switching LC-MS/MS after protein precipitation. Starting from a standard method with a quantitation limit of 0.5 ng/mL, a highly sensitive assay was developed, employing UHPLC separation and detection on an API 5000 mass spectrometer. The injected plasma equivalent was increased from 6 to 20 muL; conventional column trapping for compound enrichment and removal of matrix constituents was combined with high-pressure analytical separation using small particle columns to improve resolution and signal-to-noise ratio. Quantitation limits were thus lowered to between 5 and 20 pg/mL, offering the possibility to provide bioanalytical support for microdosing studies in humans. Excellent assay quality and robustness were achieved by both methods.
机译:本文描述了蛋白质沉淀后通过柱切换LC-MS / MS测定人血浆中的候选药物和两种代谢物的方法。从定量限为0.5 ng / mL的标准方法开始,开发了一种高灵敏度的测定方法,该方法采用UHPLC分离并在API 5000质谱仪上进行检测。注射的血浆当量从6μL增加到20μL;传统的用于化合物富集和去除基质成分的色谱柱捕集与使用小颗粒色谱柱的高压分析分离相结合,以提高分离度和信噪比。因此,定量限降低到5到20 pg / mL之间,这为为人类进行微剂量研究提供生物分析支持提供了可能性。两种方法均具有出色的测定质量和耐用性。

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