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体外代谢活化在高通量筛选中的应用。

Application of In Vitro Metabolism Activation in High-Throughput Screening.

机构信息

National Center for Advancing Translational Sciences, Division for Pre-Clinical Innovation, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Int J Mol Sci. 2020 Oct 31;21(21):8182. doi: 10.3390/ijms21218182.

Abstract

In vitro methods which incorporate metabolic capability into the assays allow us to assess the activity of metabolites from their parent compounds. These methods can be applied into high-throughput screening (HTS) platforms, thereby increasing the speed to identify compounds that become active via the metabolism process. HTS was originally used in the pharmaceutical industry and now is also used in academic settings to evaluate biological activity and/or toxicity of chemicals. Although most chemicals are metabolized in our body, many HTS assays lack the capability to determine compound activity via metabolism. To overcome this problem, several in vitro metabolic methods have been applied to an HTS format. In this review, we describe in vitro metabolism methods and their application in HTS assays, as well as discuss the future perspectives of HTS with metabolic activity. Each in vitro metabolism method has advantages and disadvantages. For instance, the S9 mix has a full set of liver metabolic enzymes, but it displays high cytotoxicity in cell-based assays. In vitro metabolism requires liver fractions or the use of other metabolically capable systems, including primary hepatocytes or recombinant enzymes. Several newly developed in vitro metabolic methods, including HepaRG cells, three-dimensional (3D) cell models, and organ-on-a-chip technology, will also be discussed. These newly developed in vitro metabolism approaches offer significant progress in dissecting biological processes, developing drugs, and making toxicology studies quicker and more efficient.

摘要

体外方法将代谢能力纳入测定中,使我们能够评估母体化合物的代谢产物的活性。这些方法可以应用于高通量筛选 (HTS) 平台,从而提高识别通过代谢过程产生活性的化合物的速度。HTS 最初用于制药行业,现在也用于学术环境中,以评估化学品的生物活性和/或毒性。尽管我们体内的大多数化学物质都被代谢,但许多 HTS 测定缺乏通过代谢确定化合物活性的能力。为了解决这个问题,已经将几种体外代谢方法应用于 HTS 格式。在这篇综述中,我们描述了体外代谢方法及其在 HTS 测定中的应用,并讨论了具有代谢活性的 HTS 的未来展望。每种体外代谢方法都有其优点和缺点。例如,S9 混合物具有全套肝脏代谢酶,但在基于细胞的测定中显示出高细胞毒性。体外代谢需要肝部分或使用其他具有代谢能力的系统,包括原代肝细胞或重组酶。还将讨论几种新开发的体外代谢方法,包括 HepaRG 细胞、三维 (3D) 细胞模型和芯片上器官技术。这些新开发的体外代谢方法在剖析生物学过程、开发药物以及使毒理学研究更快、更高效方面取得了重大进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d20a/7663506/86aa34356783/ijms-21-08182-g001.jpg

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