Development and characterisation of novel oxytocin analogues for PET imaging

The oxytocin/oxytocin receptor (OT/OTR) signalling system is involved in socioemotional behaviours, garnering interest as a therapeutic target across multiple clinical conditions. Despite its potential, our limited understanding of how to optimally target it and the scarcity of molecular tools for in vivo studies hinder therapeutic development. Molecular imaging techniques, such as Positron Emission Tomography (PET), can bridge this gap by furnishing direct insights into ligand biodistribution, receptor visualisation and ligand-receptor engagement. Here, we report the design, synthesis and biochemical and pharmacological characterisation of five OT-like peptides as novel PET tracers for investigating the OT/OTR signalling system. dOTK<sup>8</sup>[SFB] emerged as the most promising OT-like lead. The radioactive version [<sup>18</sup>F]dOTK<sup>8</sup>[SFB] was produced using a microfluidic reaction approach and validated by preclinical PET imaging of healthy rats after intravenous ligand administration. [<sup>18</sup>F]dOTK<sup>8</sup>[SFB] exhibited specific accumulation in OTR-rich tissues, affirming OTR-specificity and suitability as a new OT-like PET radiotracer for investigating OT/OTR biodistribution in humans.

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Publication Details

Journal
Communications Chemistry
Published
2025-11-05
DOI
https://doi.org/10.1038/s42004-025-01649-1
Primary Topic
Neuroendocrine regulation and behavior
Type
article
Field-Weighted Citation Impact
0.00

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article

Development and characterisation of novel oxytocin analogues for PET imaging

Adam J. Guastella, Richard B. Banati, Aleksandra Bjelosevic, Jack Markham et al.
Communications Chemistry
Neuroendocrine regulation and behavior
article

Development and characterisation of novel oxytocin analogues for PET imaging

Adam J. Guastella, Richard B. Banati, Aleksandra Bjelosevic, Jack Markham, Giancarlo Pascali, Simone Zanoni, Tiffany Mackay, Ngari Teakle, Lawson K. Spare, Markus Muttenthaler, Bo Zhang, Ivan Greguric, Lidia Matesic, Ian Bernard Hickie, Gita Rahardjo, Andrew Arthur, Alexa McDonald, Anke Hering, Mitchell A. Klenner, Larry J. Young, Arvind Parmar, Marie‐Claude Grégoire, Hasar Hamze
article en

Abstract

The oxytocin/oxytocin receptor (OT/OTR) signalling system is involved in socioemotional behaviours, garnering interest as a therapeutic target across multiple clinical conditions. Despite its potential, our limited understanding of how to optimally target it and the scarcity of molecular tools for in vivo studies hinder therapeutic development. Molecular imaging techniques, such as Positron Emission Tomography (PET), can bridge this gap by furnishing direct insights into ligand biodistribution, receptor visualisation and ligand-receptor engagement. Here, we report the design, synthesis and biochemical and pharmacological characterisation of five OT-like peptides as novel PET tracers for investigating the OT/OTR signalling system. dOTK<sup>8</sup>[SFB] emerged as the most promising OT-like lead. The radioactive version [<sup>18</sup>F]dOTK<sup>8</sup>[SFB] was produced using a microfluidic reaction approach and validated by preclinical PET imaging of healthy rats after intravenous ligand administration. [<sup>18</sup>F]dOTK<sup>8</sup>[SFB] exhibited specific accumulation in OTR-rich tissues, affirming OTR-specificity and suitability as a new OT-like PET radiotracer for investigating OT/OTR biodistribution in humans.

Communications ChemistryVol. 8(1)
The University of Sydney (AU), University of Vienna (AT), Australian Nuclear Science and Technology Organisation (AU), Emory University (US), The University of Queensland (AU), Liverpool Hospital (AU), Children's Hospital at Westmead (AU), UNSW Sydney (AU), Centre for Quantum Computation and Communication Technology (AU), Canadian Nuclear Laboratories (CA), Stanford University (US)
Australian Nuclear Science and Technology Organisation, National Imaging Facility, European Commission
Openalex Percentile: Top 63%
Neuroendocrine regulation and behavior
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