Evidence map›Paper›PMID 33572353›Full record

ArticleMolecules (Basel, Switzerland)2021

Preliminary Study of a 1,5-Benzodiazepine-Derivative Labelled with Indium-111 for CCK-2 Receptor Targeting.

Marco Verona, Sara Rubagotti, Stefania Croci, Sophia Sarpaki, Francesca Borgna, Marianna Tosato, Elisa Vettorato, Giovanni Marzaro, Francesca Mastrotto, Mattia Asti

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.1field-weighted citation impact, top 13% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
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  4. Article
  5. Article
  6. Review
  7. Metal-Based Radiopharmaceuticals in Inorganic Chemistry.Molecules (Basel, Switzerland) · 2023
    Article
  8. Article
  9. Review
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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

10 authors at 3 institutions in 2 countries.

Marco VeronaDepartment of Pharmaceutical Sciences, University of Padova, via Marzolo 5, 35131 Padova, Italy.
Sara RubagottiRadiopharmaceutical Chemistry Section, Nuclear Medicine Unit, AUSL-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42122 Reggio Emilia, Italy.
Stefania CrociClinical Immunology, Allergy, and Advanced Biotechnologies Unit, Diagnostic Imaging and Laboratory Medicine Department, AUSL-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42122 Reggio Emilia, Italy.ORCID 0000-0002-8622-0439
Sophia SarpakiBioemtech, Lefkippos Attica Technology Park N.C.S.R. "DEMOKRITOS" Patr. Gregoriou E & 27 Neapoleos Str. Ag. Paraskevi, 15341 Athens, Greece.ORCID 0000-0003-4323-3165
Francesca BorgnaDepartment of Pharmaceutical Sciences, University of Padova, via Marzolo 5, 35131 Padova, Italy.
Marianna TosatoDepartment of Chemical Sciences, University of Padova, via Marzolo 1, 35131 Padova, Italy.
Elisa VettoratoDepartment of Pharmaceutical Sciences, University of Padova, via Marzolo 5, 35131 Padova, Italy.
Giovanni MarzaroDepartment of Pharmaceutical Sciences, University of Padova, via Marzolo 5, 35131 Padova, Italy.ORCID 0000-0002-5892-5992
Francesca MastrottoDepartment of Pharmaceutical Sciences, University of Padova, via Marzolo 5, 35131 Padova, Italy.ORCID 0000-0002-2499-5490
Mattia AstiRadiopharmaceutical Chemistry Section, Nuclear Medicine Unit, AUSL-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42122 Reggio Emilia, Italy.
University of Padua · ITAzienda Sanitaria Unità Locale di Reggio Emilia · ITNational Centre of Scientific Research "Demokritos" · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cholecystokinin-2 receptor (CCK-2R) is overexpressed in several human cancers but displays limited expression in normal tissues. For this reason, it is a suitable target for developing specific radiotracers. In this study, a nastorazepide-based ligand functionalized with a 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) chelator (IP-001) was synthesized and labelled with indium-111. The radiolabeling process yielded >95% with a molar activity of 10 MBq/nmol and a radiochemical purity of >98%. Stability studies have shown a remarkable resistance to degradation (>93%) within 120 h of incubation in human blood. The in vitro uptake of [

Indexed as

AnimalsApoptosisBenzodiazepinesCell ProliferationFemaleHumansIndium RadioisotopesLung NeoplasmsMiceMice, Inbred BALB CMice, NudeRadiopharmaceuticalsReceptor, Cholecystokinin BTissue DistributionTomography, Emission-Computed, Single-PhotonTumor Cells, CulturedBenzodiazepinesIndium-111Indium RadioisotopesRadiopharmaceuticalsReceptor, Cholecystokinin Bcholecystokinin-2 receptorindium-111 labellingnastorazepideradiopharmaceuticals

Identifiers

PMID33572353
PMCPMC7916174
OpenAlexW3127217725

What OpenQuestion holds

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Registered trials

None linked

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.