Evidence map›Paper›PMID 24163019›Full record

ArticleMolecular imaging and biology2014

Radiosynthesis of [124I]iodometomidate and biological evaluation using small-animal PET.

Herbert Kvaternik, Thomas Wanek, Friedrich Hammerschmidt, Ilse Zolle, Reingard Aigner, Claudia Kuntner

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Article in Molecular imaging and biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Herbert KvaternikDivision of Nuclear Medicine, Medical University of Graz, Auenbruggerplatz 9, 8036, Graz, Austria, herbert.kvaternik@medunigraz.at.
Thomas Wanek
Friedrich Hammerschmidt
Ilse Zolle
Reingard Aigner
Claudia Kuntner

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe application of radiolabelled inhibitors of cytochrome P450 enzymes is a novel approach for molecular imaging of adrenocortical masses to detect adrenal tumours. One potential tracer is radiolabelled iodometomidate (IMTO) with a common option for scintigraphic diagnosis and therapeutic applications. The aim of this study was to radiolabel iodometomidate with the positron-emitting radionuclide iodine-124 ((124)I) for the investigation of the biological behaviour and pharmacokinetics with positron emission tomography (PET). PROCEDURES: [(124)I]IMTO has been synthesized by oxidative radioiodo-destannylation, purified via semi-preparative HPLC and formulated in acetate-buffered saline, which contained ascorbic acid and ethanol to avoid radiolytic decomposition. Biological evaluation was performed in rats which received 5.5 ± 0.7 MBq [(124)I]IMTO in vivo. The radioactivity distribution (n = 3) has been dynamically imaged from 0-120 min after intravenous (i.v.) injection by small-animal PET. Regions of interest have been defined manually in the reconstructed PET images, and the activity concentration was expressed as percent injected dose per gram tissue (%ID/g).

results[(124)I]IMTO was prepared with a radiochemical yield of 83 ± 5 % (n = 3) and a radiochemical purity of >97 %. The final formulation of [(124)I]IMTO was stable for up to 48 h at room temperature. Two hours after i.v. administration in rats, radioactivity concentration in the adrenal glands were 2.1 ± 0.3 %ID/g, which was sufficient to achieve highest-contrast adrenal PET images.

conclusionsIn the present study, the biological characteristics of radioiodinated metomidate were evaluated. [(124)I]IMTO appears as an attractive PET tracer for imaging of adrenals.

Indexed as

AnimalsEtomidateFemaleIodine RadioisotopesPositron-Emission TomographyRatsRats, Sprague-DawleyTissue DistributionEtomidateIodine Radioisotopesiodophenyl metomidate

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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.