GlaxoSmithKline, Via Fleming 2, 37135 Verona, Italy.
Expert Opin Drug Metab Toxicol. 2011 Feb;7(2):137-46. doi: 10.1517/17425255.2011.545053.
Drug blood (or plasma) levels measured during safety preclinical investigations do not always correlate with toxicological findings. Concentrations in target tissues or, even better, at target receptors would probably be more relevant. In addition, toxicity may be caused by drug metabolites which, in turn, can be tissue specific. Tissue concentrations and tissue metabolism may be crucial for interpreting tissue toxicity.
This paper, starting from the authors' direct experience, focuses on distribution of the parent compound and metabolites in target toxicity tissues and presents a review of several examples where organ or tissue concentrations have been either useful or not relevant for interpreting safety findings. Regulatory aspects and technological progresses are also mentioned.
The authors advocate directing more attention and efforts toward investigating tissue distribution: this approach might reduce late stage attrition. When unexpected tissue toxicity is found, measuring drug concentrations in the target tissue and characterising and measuring tissue metabolites could bring relevant information for interpreting the adverse finding. Evidence of slow accumulation of a long lasting metabolite in a tissue should be considered as an alert: this evidence can be obtained during short-term toxicity studies.
在安全性临床前研究中测量的药物血(或血浆)水平并不总是与毒理学发现相关。在靶组织中的浓度,或者更好的是,在靶受体中的浓度可能会更相关。此外,毒性可能是由药物代谢物引起的,而这些代谢物反过来又可能具有组织特异性。组织浓度和组织代谢对于解释组织毒性可能至关重要。
本文从作者的直接经验出发,重点介绍了母体化合物和代谢物在靶毒性组织中的分布,并回顾了几个例子,其中器官或组织浓度对于解释安全性发现是有用的或不相关的。还提到了监管方面和技术进展。
作者主张将更多的注意力和精力集中在研究组织分布上:这种方法可能会减少后期淘汰。当发现意外的组织毒性时,测量靶组织中的药物浓度,并对组织代谢物进行特征分析和测量,可以为解释不良发现提供相关信息。在组织中缓慢积累持久代谢物的证据应被视为警报:这种证据可以在短期毒性研究中获得。