Jekunen A P, Pauwels E K J, Kairemo K J A
Oncology Unit, Kokkola Central Hospital, 67200 Kokkola, Finland.
Bioanalysis. 2010 Mar;2(3):421-8. doi: 10.4155/bio.09.189.
Microdosing provides a tool to enhance drug development by initiating human studies prior to Phase I studies. The purpose is to assist in the go versus no-go decision-making process and to eliminate early ineffective compounds from the drug pipeline. Selection of multiple potential leads can be performed at the clinical stage instead of in preclinical studies. The microdosing approach can be easily used for a molecularly targeted potential drug compound with a known mechanism of action. It provides useful data regarding accessibility and biodistribution that can be used in many estimations benefiting the development of the molecule. In addition, steady state and genetic investigations are becoming possible. Microdosing has a sparing effect on timelines and costs, however, the real importance is not yet known because, although it is known to be widely performed, only a few original reports have been published.
微剂量给药提供了一种工具,可通过在I期研究之前启动人体研究来加速药物开发。其目的是协助进行继续或终止的决策过程,并从药物研发流程中剔除早期无效的化合物。可以在临床阶段而非临床前研究阶段对多种潜在先导化合物进行筛选。微剂量给药方法可轻松应用于具有已知作用机制的分子靶向潜在药物化合物。它提供了有关可及性和生物分布的有用数据,可用于许多评估中,从而有利于该分子的开发。此外,稳态和遗传学研究也变得可行。微剂量给药对时间和成本具有节省作用,然而,其真正的重要性尚不清楚,因为尽管已知该方法被广泛应用,但仅发表了少数原始报告。