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早期药物研发中用于检测药物诱导的不良变力性效应的基于细胞的检测平台的考量。第1部分:新型检测平台开发的一般考量。

Considerations for an , Cell-Based Testing Platform for Detection of Adverse Drug-Induced Inotropic Effects in Early Drug Development. Part 1: General Considerations for Development of Novel Testing Platforms.

作者信息

Guth Brian D, Engwall Michael, Eldridge Sandy, Foley C Michael, Guo Liang, Gintant Gary, Koerner John, Parish Stanley T, Pierson Jennifer B, Ribeiro Alexandre J S, Zabka Tanja, Chaudhary Khuram W, Kanda Yasunari, Berridge Brian

机构信息

Department of Drug Discovery Sciences, Boehringer Ingelheim Pharma GmbH & Co KG, Biberach an der Riss, Germany.

PreClinical Drug Development Platform (PCDDP), North-West University, Potchefstroom, South Africa.

出版信息

Front Pharmacol. 2019 Aug 9;10:884. doi: 10.3389/fphar.2019.00884. eCollection 2019.

Abstract

Drug-induced effects on cardiac contractility can be assessed through the measurement of the maximal rate of pressure increase in the left ventricle (LVdP/dt) in conscious animals, and such studies are often conducted at the late stage of preclinical drug development. Detection of such effects earlier in drug research using simpler, test systems would be a valuable addition to our strategies for identifying the best possible drug development candidates. Thus, testing platforms with reasonably high throughput, and affordable costs would be helpful for early screening purposes. There may also be utility for testing platforms that provide mechanistic information about how a given drug affects cardiac contractility. Finally, there could be testing platforms that could ultimately contribute to the regulatory safety package of a new drug. The characteristics needed for a successful cell or tissue-based testing platform for cardiac contractility will be dictated by its intended use. In this article, general considerations are presented with the intent of guiding the development of new testing platforms that will find utility in drug research and development. In the following article (part 2), specific aspects of using human-induced stem cell-derived cardiomyocytes for this purpose are addressed.

摘要

药物对心脏收缩力的影响可以通过测量清醒动物左心室压力增加的最大速率(LVdP/dt)来评估,此类研究通常在临床前药物研发的后期进行。在药物研究的早期阶段,使用更简单的测试系统检测此类影响,将是我们筛选最佳药物研发候选物策略的一项有价值的补充。因此,具有合理高通量且成本可控的测试平台将有助于早期筛选。提供关于特定药物如何影响心脏收缩力的机制信息的测试平台可能也有用处。最后,可能存在能够最终为新药的监管安全包做出贡献的测试平台。成功的基于细胞或组织的心脏收缩力测试平台所需的特性将由其预期用途决定。本文提出了一些总体考量,旨在指导新测试平台的开发,这些平台将在药物研发中发挥作用。在接下来的文章(第2部分)中,将探讨为此目的使用人诱导多能干细胞衍生的心肌细胞的具体方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8be4/6697071/fe4d5fb3c4fb/fphar-10-00884-g001.jpg

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