4.7 Review

Imaging techniques to study drug transporter function in vivo

Journal

PHARMACOLOGY & THERAPEUTICS
Volume 189, Issue -, Pages 104-122

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pharmthera.2018.04.006

Keywords

Pharmacokinetics; Molecular imaging; Membrane transporters; Positron emission tomography; Magnetic resonance imaging; Single photon emission computed tomography

Funding

  1. French National Research Agency [ANR-16-CE17-0011-001]
  2. Swiss National Science Foundation (SNF) [310030_166563]
  3. SNF National Center of Competence in Research TransCure (University of Berne, Switzerland)
  4. Austrian Science Fund (FWF) [F 3513-B11, F 3513-B20, P24894-B24, I 1609-B24, KLI-480-B30]
  5. Lower Austria Corporation for Research and Education (NFB) [LS12-006, LS15-003]
  6. European Community [201380]
  7. [ANR-11-INBS-0006]

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Transporter systems involved in the permeation of drugs and solutes across biological membranes are recognized as key determinants of pharmacokinetics. Typically, the action of membrane transporters on drug exposure to tissues in living organisms is inferred from invasive procedures, which cannot be applied in humans. In recent years, imaging methods have greatly progressed in terms of instruments, synthesis of novel imaging probes as well as tools for data analysis. Imaging allows pharmacokinetic parameters in different tissues and organs to be obtained in a non-invasive or minimally invasive way. The aim of this overview is to summarize the current status in the field of molecular imaging of drug transporters. The overview is focused on human studies, both for the characterization of transport systems for imaging agents as well as for the determination of drug pharmacokinetics, and makes reference to animal studies where necessary. We conclude that despite certain methodological limitations, imaging has a great potential to study transporters at work in humans and that imaging will become an important tool, not only in drug development but also in medicine. Imaging allows the mechanistic aspects of transport proteins to be studied, as well as elucidating the influence of genetic background, pathophysiological states and drug-drug interactions on the function of transporters involved in the disposition of drugs. (C) 2018 Elsevier Inc. All rights reserved.

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