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Big physics, small doses: the use of AMS and PET in human microdosing of development drugs

Graham Lappin, R. Colin Garner

Nature Reviews Drug Discovery February 28, 2003 DOI: 10.1038/nrd1037 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Review Peer reviewed
Topics Microdosing
Keywords Investigational drugs Drug discovery Drug development Pharmacology Pharmacokinetics Preclinical research Pharmacodynamics Positron emission tomography Human use Medical physics Computational biology Clinical trial Bioinformatics Nuclear medicine Biotechnology
Citations 257
Key findings Microdosing, using PET and AMS, enables earlier human testing of investigational drugs, reducing failure rates and animal use.

Abstract

The process of early clinical drug development has changed little over the past 20 years despite an up to 40% failure rate associated with inappropriate drug metabolism and pharmacokinetics of candidate molecules. A new method of obtaining human metabolism data known as microdosing has been developed which will permit smarter candidate selection by taking investigational drugs into humans earlier. Microdosing depends on the availability of two ultrasensitive 'big-physics' techniques: positron emission tomography (PET) can provide pharmacodynamic information, whereas accelerator mass spectrometry (AMS) provides pharmacokinetic information. Microdosing allows safer human studies as well as reducing the use of animals in preclinical toxicology.

Comparable studies

Other narrative reviews on microdosing, most cited first.

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