Attia Sabry M
Department of Pharmacology and Toxicology; College of Pharmacy; King Saud University; Riyadh, Saudi Arabia.
Oxid Med Cell Longev. 2010 Jul-Aug;3(4):238-53. doi: 10.4161/oxim.3.4.13246.
A number of drugs have been withdrawn from the market or severely restricted in their use because of unexpected toxicities that become apparent only after the launch of new drug entities. Circumstantial evidence suggests that, in most cases, reactive metabolites are responsible for these unexpected toxicities. In this review, a general overview of the types of reactive metabolites and the consequences of their formation are presented. The current approaches to evaluate bioactivation potential of new compounds with particular emphasis on the advantages and limitation of these procedures will be discussed. Reasonable reasons for the excellent safety record of certain drugs susceptible to bioactivation will also be explored and should provide valuable guidance in the use of reactive-metabolite assessments when nominating drug candidates for development. This will, in turn, help us to design and bring safer drugs to the market.
由于一些新药实体上市后才显现出意外毒性,许多药物已被撤出市场或其使用受到严格限制。间接证据表明,在大多数情况下,反应性代谢物是这些意外毒性的原因。在本综述中,将对反应性代谢物的类型及其形成的后果进行概述。将讨论评估新化合物生物活化潜力的当前方法,特别强调这些程序的优缺点。还将探讨某些易发生生物活化的药物具有出色安全记录的合理原因,这在提名药物候选物进行开发时使用反应性代谢物评估方面应提供有价值的指导。反过来,这将帮助我们设计并将更安全的药物推向市场。