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In vitro approaches to investigate cytochrome P450 activities: Update on current status and their applicability

机译:体外研究细胞色素P450活性的方法:最新进展及其适用性

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Introduction: Cytochromes P450 (CYPs) play a central role in the Phase I metabolism of drugs and other xenobiotics. It is estimated that CYPs can metabolize up to two-thirds of drugs present in humans. Over the past two decades, there have been numerous advances in in vitro methodologies to characterize drug metabolism and interaction involving CYPs. Areas covered: This review focuses on the use of in vitro methodologies to examine CYPs' role in drug metabolism and interaction. There is an emphasis on their current development, applicability, advantages and limitations as well as the use of in silico approaches in complementing and supporting in vitro data. The article also highlights the challenges in extrapolating in vitro data to in vivo situations. Expert opinion: Advances in in vitro methodologies have been made such that data can be used for in vivo prediction with comfortable degree of confidence. Improved assay designs and analytical techniques have permitted development of miniaturized assay format and automated system with improved sensitivity and throughput capacity. High-quality experimental designs and scientifically rigorous assessment/validation protocols remain crucial in developing reliable and robust in vitro models. With continued progress made in the field, in vitro methodologies will continually be employed in evaluating CYP activities in pharmaceutical industries and laboratories.
机译:简介:细胞色素P450(CYP)在药物和其他异源生物的I期代谢中起着核心作用。据估计,CYPs最多可以代谢人类中三分之二的药物。在过去的二十年中,用于表征涉及CYP的药物代谢和相互作用的体外方法学取得了许多进步。涵盖的领域:这篇综述着重于使用体外方法来研究CYP在药物代谢和相互作用中的作用。重点介绍了它们的当前发展,适用性,优点和局限性,以及计算机技术在补充和支持体外数据中的应用。本文还强调了将体外数据外推到体内情况的挑战。专家意见:体外方法学已取得进展,因此可以将数据用于舒适的体内预测。改进的测定设计和分析技术已允许开发具有改进的灵敏度和通量的小型化测定形式和自动化系统。高质量的实验设计和科学严谨的评估/验证协议对于开发可靠而强大的体外模型仍然至关重要。随着该领域的不断进步,体外方法将继续用于评估制药行业和实验室中的CYP活性。

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