Evidence map›Paper›PMID 19616318›Full record

ReviewTrends in pharmacological sciences2009

PET radiotracers: crossing the blood-brain barrier and surviving metabolism.

Victor W Pike

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Trends in pharmacological sciences, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03705819 (Exploratory Evaluation of [11C]-NOP46 Pharmacokinetics With Positron Emission Tomography), which is not on this map. Cited by 243 papers.

0numbers the graph read from it
0cells of the map it votes in
243citing papers in PubMed
10.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03705819 early_phase1completednot on this mapstarted 2019, after this paper: background citation

Exploratory Evaluation of [11C]-NOP46 Pharmacokinetics With Positron Emission Tomography (PET)

TypeinterventionalSponsorColumbia UniversityRan2019 to 2023Enrolled10ConditionsChronic PainArms[11C]-NOP46, PET/CT scan
3 · Its place in the literature

Who cites it

243 citing papers in PubMed, 567 citations in OpenAlex.

  1. Longitudinal evaluation of surrogates of regional cerebral blood flow computed from dynamic amyloid PET imaging.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2020
    Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Advances in GPCR-Targeted PET Radiotracer Patents (2020-2025).Pharmaceuticals (Basel, Switzerland) · 2026
    Review
  8. Article
  9. Article
  10. Article
  11. A Study of 3-Substituted 7-Methoxy-2,3,4,5-tetrahydro-1Molecules (Basel, Switzerland) · 2026
    Article
  12. PET imaging of alpha-synuclein: from radiotracer design through in vitro and in vivo translation.European journal of nuclear medicine and molecular imaging · 2026
    Review
  13. Article
  14. Article
  15. Review
  16. Trifluoromethylation of alkyl electrophiles withScience (New York, N.Y.) · 2025
    Article
  17. Review
  18. Development of [Nature communications · 2025
    Article
  19. Review
  20. Article

183 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Victor W PikeMolecular Imaging Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA. pikev@mail.nih.gov
National Institute of Mental Health · US

Funding

PET Radiopharmaceutical SciencesZIAMH002793 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI PIKE, VICTOR W · 2009 to 2025
$69.8M
PET Radiopharmaceutical SciencesZ01MH002793 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI PIKE, VICTOR W · 2002 to 2008
$7.4M
Intramural NIH HHS Z01 MH002793Intramural NIH HHS ZIA MH002793NIMH NIH HHS Z01 MH 002793
6 · The paper itself

Abstract

Radiotracers for imaging protein targets in the living human brain with positron emission tomography (PET) are increasingly useful in clinical research and in drug development. Such radiotracers must fulfill many criteria, among which an ability to enter brain adequately and reversibly without contamination by troublesome radiometabolites is desirable for accurate measurement of the density of a target protein (e.g. neuroreceptor, transporter, enzyme or plaque). Candidate radiotracers can fail as a result of poor passive brain entry, rejection from brain by efflux transporters or undesirable metabolism. These issues are reviewed. Emerging PET radiotracers for measuring efflux transporter function and new strategies for ameliorating radiotracer metabolism are discussed. A growing understanding of the molecular features affecting the brain penetration, metabolism and efflux transporter sensitivity of prospective radiotracers should ultimately lead to their more rational and efficient design, and also to their greater efficacy.

Indexed as

Radioactive TracersAnimalsBlood-Brain BarrierBrainDrug Delivery SystemsHumansMembrane Transport ProteinsModels, BiologicalMolecular StructurePositron-Emission TomographyRadiopharmaceuticalsMembrane Transport ProteinsRadioactive TracersRadiopharmaceuticals

Identifiers

PMID19616318
PMCPMC2805092
OpenAlexW2103312948

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.