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首页> 外文期刊>Chemistry Letters >A New Physiologically Based Pharmacokinetic Analysis for In Vivo Organ Disposition of Nitroxyl Spin Probes in Mice as Measured by Multisite Detection L-band ESR (MSD-LESR)
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A New Physiologically Based Pharmacokinetic Analysis for In Vivo Organ Disposition of Nitroxyl Spin Probes in Mice as Measured by Multisite Detection L-band ESR (MSD-LESR)

机译:一种新的基于生理的药代动力学分析,通过多位点检测L波段ESR(MSD-LESR)测量小鼠体内硝基氧自旋探针的体内器官处置

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摘要

We developed a physiologically based pharmacokinetic (PB-PK)model for spin-labeled drugs in animals and applied it for analyzing the decay curves of spin probes in the organs of mice as measured by multisite detection L-band ESR (MSD-LESR).The proposed method will be useful for not only understanding the PK features of nitroxyl radicals as spin probes but also developing spin-labeled drugs as a substitute for radio-isotope-labeled drugs.
机译:我们为动物中的自旋标记药物开发了基于生理学的药代动力学(PB-PK)模型,并将其用于分析小鼠器官中自旋探针的衰减曲线,该曲线通过多位点检测L波段ESR(MSD-LESR)测量。所提出的方法不仅可用于理解作为旋转探针的硝酰基自由基的PK特征,而且可用于开发自旋标记的药物来替代放射性同位素标记的药物。

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