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用于人体早期生物动力学研究的微剂量给药。

Microdosing for early biokinetic studies in humans.

作者信息

Stenström K, Sydoff M, Mattsson S

机构信息

Department of Physics, Division of Nuclear Physics, Lund University, PO Box 118, SE-221 00 Lund, Sweden.

出版信息

Radiat Prot Dosimetry. 2010 Apr-May;139(1-3):348-52. doi: 10.1093/rpd/ncq029. Epub 2010 Feb 18.

Abstract

Microdosing is a new concept in drug development that--if implemented in the pharmaceutical industry--would mean that new drugs can be tested earlier in humans than done today. The human microdosing concept--or 'Phase 0'--may offer improved candidate selection, reduced failure rates in the drug development line and a reduction in the use of laboratory animals in early drug development, factors which will help to speed up drug development and also reduce the costs. Microdosing utilises sub-pharmacological amounts of the substance to open opportunities for early studies in man. Three technologies are used for microdosing: accelerator mass spectrometry (AMS), positron emission tomography and liquid chromatography-tandem mass spectrometry. This paper focuses on the principle of AMS and discusses the current status of microdosing with AMS.

摘要

微剂量给药是药物研发中的一个新概念,若在制药行业得以实施,意味着新药可在人体上比目前更早进行测试。人体微剂量给药概念(即“0期”)可能会改善候选药物的筛选,降低药物研发流程中的失败率,并减少早期药物研发中实验动物的使用,这些因素将有助于加快药物研发速度并降低成本。微剂量给药利用亚药理剂量的物质为人体早期研究创造机会。微剂量给药采用三种技术:加速器质谱法(AMS)、正电子发射断层扫描和液相色谱 - 串联质谱法。本文重点介绍加速器质谱法的原理,并讨论使用加速器质谱法进行微剂量给药的现状。

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