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Microdosing, isotopic labeling, radiotracers and metabolomics: Relevance in drug discovery, development and safety

Journal Article


Abstract


  • This review discusses the use of stable (13C, 2D) or radioactive isotopes (14C,11C, 18F, 131I, 64Cu, 68Ga) incorporated into the molecular structure of new drug entities for the purpose of pharmacokinetic or -dynamic studies. Metabolite in safety testing requires the administration of pharmacologically active doses. In such studies, radiotracers find application mainly in preclinical animal investigations, whereby LC-MS/MS is used to identify metabolite structure and drug-related effects. In contrast, first-in-human metabolite studies have to be carried out at nonpharmacological doses not exceeding 100 μg (microdose), which is generally too low for metabolite detection by LC-MS/MS. This short-coming can be overcome by specific radio- or isotopic labeling of the drug of interest and measurements using accelerator mass spectroscopy, single-photon emission computed tomography and positron emission tomography. Such combined radioisotope-based approaches permit Phase 0, first-in-human metabolite study.

Publication Date


  • 2017

Citation


  • Wotherspoon, A. T. L., Safavi-Naeini, M., & Banati, R. B. (2017). Microdosing, isotopic labeling, radiotracers and metabolomics: Relevance in drug discovery, development and safety. Bioanalysis, 9(23), 1913-1933. doi:10.4155/bio-2017-0137

Scopus Eid


  • 2-s2.0-85044230103

Start Page


  • 1913

End Page


  • 1933

Volume


  • 9

Issue


  • 23

Abstract


  • This review discusses the use of stable (13C, 2D) or radioactive isotopes (14C,11C, 18F, 131I, 64Cu, 68Ga) incorporated into the molecular structure of new drug entities for the purpose of pharmacokinetic or -dynamic studies. Metabolite in safety testing requires the administration of pharmacologically active doses. In such studies, radiotracers find application mainly in preclinical animal investigations, whereby LC-MS/MS is used to identify metabolite structure and drug-related effects. In contrast, first-in-human metabolite studies have to be carried out at nonpharmacological doses not exceeding 100 μg (microdose), which is generally too low for metabolite detection by LC-MS/MS. This short-coming can be overcome by specific radio- or isotopic labeling of the drug of interest and measurements using accelerator mass spectroscopy, single-photon emission computed tomography and positron emission tomography. Such combined radioisotope-based approaches permit Phase 0, first-in-human metabolite study.

Publication Date


  • 2017

Citation


  • Wotherspoon, A. T. L., Safavi-Naeini, M., & Banati, R. B. (2017). Microdosing, isotopic labeling, radiotracers and metabolomics: Relevance in drug discovery, development and safety. Bioanalysis, 9(23), 1913-1933. doi:10.4155/bio-2017-0137

Scopus Eid


  • 2-s2.0-85044230103

Start Page


  • 1913

End Page


  • 1933

Volume


  • 9

Issue


  • 23