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首页> 外文期刊>Xenobiotica: the fate of foreign compounds in biological systems >Leveraging model-based study designs and serial micro-sampling techniques to understand the oral pharmacokinetics of the potent LTB4 inhibitor, CP-105696, for mouse pharmacology studies
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Leveraging model-based study designs and serial micro-sampling techniques to understand the oral pharmacokinetics of the potent LTB4 inhibitor, CP-105696, for mouse pharmacology studies

机译:利用基于模型的研究设计和连续微抽样技术,了解有效LTB4抑制剂CP-105696的口腔药代动力学,用于小鼠药理学研究

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摘要

1.Leukotriene B4 (LTB4) is a proinflammatory mediator important in the progression of a number of inflammatory diseases. Preclinical models can explore the role of LTB4 in pathophysiology using tool compounds, such as CP-105696, that modulate its activity. To support preclinical pharmacology studies, micro-sampling techniques and mathematical modeling were used to determine the pharmacokinetics of CP-105696 in mice within the context of systemic inflammation induced by a high-fat diet (HFD).
机译:1.Leukotriene B4(LTB4)是一种在许多炎症疾病的进展中重要的促炎介质。 临床前模型可以使用刀具化合物(例如CP-105696)探讨LTB4在病理生理学中的作用,例如CP-105696,CP-105696调节其活性。 为了支持临床前药理学研究,微抽样技术和数学建模用于在高脂饮食(HFD)诱导的全身炎症的背景下确定小鼠CP-105696的药代动力学。

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