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Sökning: id:"swepub:oai:DiVA.org:uu-438420" > Para-chloro-2-[18F]...

Para-chloro-2-[18F]fluoroethyl-etomidate : A promising new PET radiotracer for adrenocortical imaging

Silins, Isabella, 1983- (författare)
Uppsala universitet,Endokrinkirurgi
Sundin, Anders, 1954- (författare)
Uppsala universitet,Radiologi
Nordeman, Patrik, Docent (författare)
Uppsala universitet,Preparativ läkemedelskemi
visa fler...
Jahan, Mahabuba (författare)
Uppsala universitet,Preparativ läkemedelskemi
Estrada, Sergio (författare)
Uppsala universitet,Preparativ läkemedelskemi
Monazzam, Azita, 1971- (författare)
Uppsala universitet,Endokrin tumörbiologi
Lubberink, Mark (författare)
Uppsala universitet,Radiologi
Aigbirhio, Franklin (författare)
Wolfson Brain Imaging Centre, University of Cambridge
Hellman, Per (författare)
Uppsala universitet,Endokrinkirurgi
Antoni, Gunnar (författare)
Uppsala universitet,Preparativ läkemedelskemi
visa färre...
 (creator_code:org_t)
Ivyspring International Publisher, 2021
2021
Engelska.
Ingår i: International Journal of Medical Sciences. - : Ivyspring International Publisher. - 1449-1907. ; 18:10, s. 2187-2196
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Introduction: [11C]Metomidate ([11C]MTO), the methyl ester analogue of etomidate, was developed as a positron emission tomography (PET) radiotracer for adrenocortical tumours and has also been suggested for imaging in primary aldosteronism (PA). A disadvantage of [11C]MTO is the rather high non-specific binding in the liver, which impacts both visualization and quantification of the uptake in the right adrenal gland. Furthermore, the short 20-minute half-life of carbon-11 is a logistic challenge in the clinical setting.Objectives: The aim of this study was to further evaluate the previously published fluorine-18 (T1/2=109.5 min) etomidate analogue, para-chloro-2-[18F]fluoroethyl etomidate; [18F]CETO, as an adrenal PET tracer.Methods: In vitro experiments included autoradiography on human and cynomolgus monkey (non-human primate, NHP) tissues and binding studies on adrenal tissue from NHPs. In vivo studies with [18F]CETO in mice, rats and NHP, using PET and CT/MRI, assessed biodistribution and binding specificity in comparison to [11C]MTO.Results: The binding of [18F]CETO in the normal adrenal cortex, as well as in human adrenocortical adenomas and adrenocortical carcinomas, was shown to be specific, both in vitro (in humans) and in vivo (in rats and NHP) with an in vitro Kd of 0.66 nM. Non-specific uptake of [18F]CETO in NHP liver was found to be low compared to that of [11C]MTO.Conclusions: High specificity of [18F]CETO to the adrenal cortex was demonstrated, with in vivo binding properties qualitatively surpassing those of [11C]MTO. Non-specific binding to the liver was significantly lower than that of [11C]MTO. [18F]CETO is a promising new PET tracer for imaging of adrenocortical disease and should be evaluated further in humans.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Radiologi och bildbehandling (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Radiology, Nuclear Medicine and Medical Imaging (hsv//eng)

Nyckelord

18F-CETO
Adrenal masses
Adrenal tracer
Positron emission tomography
Primary aldosteronism
Radiology
Radiologi

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