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  4. 68Ga-NODAGA-RGDyK for αvβ3 integrin PET imaging. Preclinical investigation and dosimetry.
 
  • Détails
Titre

68Ga-NODAGA-RGDyK for αvβ3 integrin PET imaging. Preclinical investigation and dosimetry.

Type
article
Institution
UNIL/CHUV/Unisanté + institutions partenaires
Périodique
Nuclear Medicine  
Auteur(s)
Buchegger, F.
Auteure/Auteur
Viertl, D.
Auteure/Auteur
Baechler, S.
Auteure/Auteur
Dunet, V.
Auteure/Auteur
Kosinski, M.
Auteure/Auteur
Poitry-Yamate, C.
Auteure/Auteur
Rüegg, C.
Auteure/Auteur
Prior, J.O.
Auteure/Auteur
Liens vers les personnes
Buchegger, Franz  
Prior, John  
Baechler, Sebastien  
Dosne, Philippe  
Ruegg, Curzio  
Dunet, Vincent  
Liens vers les unités
Radiophysique  
Méd. nucléaire et imagerie molécul.  
Centre pluridiscip. d'oncologie clinique  
ISSN
0029-5566
Statut éditorial
Publié
Date de publication
2011
Volume
50
Numéro
6
Première page
225
Dernière page/numéro d’article
233
Peer-reviewed
Oui
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Résumé
To visualize neovasculature and/or tumour integrin αvβ3 we selected the binding moiety Arg-Gly-Asp-D-Tyr-Lys (RGDyK) coupled to NODAGA for labeling with 68Ga.
NODAGA-RGDyK (ABX) was labeled with the 68Ga eluate from the 68Ge generator IGG100 using the processor unit PharmTracer. Biodistribution was measured in female Hsd mice sacrificed 10, 30, 60 and 90 min after i.v. injection of 68Ga-NODAGA-RGDyK for OLINDA dosimetry extrapolated to humans. Tumour targeting was studied in SCID mice bearing A431 and other tumour transplants using microPET and biodistribution measurements.
Effective half-life of 68Ga-NODAGA-RGDyK was ~25 min for total body and most organs except liver and spleen that showed stable activity retention. With a bladder voiding interval of 0.5 h the calculated effective dose (ED) was 0.012 and 0.016 mSv/MBq for males and females, respectively. Rapid uptake within 10 min was observed in A431 tumours with dynamic PET followed by a slow release. Biodistribution measurements showed a 68Ga-NODAGA-RGDyK uptake in A431 tumours of 3.4±0.4 and 2.7±0.3%ID/g at 1 and 2 h, respectively. Similar uptakes were observed in a mouse and human breast and ovarian cancer xenografts. Co-injection of excess (5 mg/kg) unlabeled NODAGA-RGDyK with the radiotracer reduced tumour uptake at one hour to 0.23±0.01%ID/g, but similarly decreased uptake in normal organs as well. When unlabeled peptide was injected 15 min after 68Ga-NODAGA-RGDyK, uptake diminished particularly in tumour and adrenals, suggestive of a different binding mode compared with other normal tissues.
NODAGA-RGDyK was reliably labeled with 68Ga and revealed a predicted ED of 0.014 mSv/MBq. Tumour uptake was rapid and significant and was chased with unlabeled RGDyK in a similar manner as adrenal uptake.
Sujets

Animals

Body Burden

Carcinoma, Squamous C...

Carcinoma, Squamous C...

Cell Line, Tumor

Drug Evaluation, Prec...

Female

Gallium Radioisotopes...

Heterocyclic Compound...

Heterocyclic Compound...

Humans

Integrin alphaVbeta3/...

Integrin alphaVbeta3/...

Metabolic Clearance R...

Mice

Mice, Inbred ICR

Oligopeptides/pharmac...

Organ Specificity

Positron-Emission Tom...

Radiopharmaceuticals/...

Radiopharmaceuticals/...

Reproducibility of Re...

Sensitivity and Speci...

Whole-Body Counting

PID Serval
serval:BIB_B0DFD4BA9EE2
DOI
10.3413/Nukmed-0416-11-06
PMID
21989840
WOS
000299030500002
Permalien
https://iris.unil.ch/handle/iris/187648
Date de création
2012-02-15T14:58:26.114Z
Date de création dans IRIS
2025-05-21T01:33:08Z
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