Stable 211At-labeled radiopharmaceuticals for targeted α therapy

The SAt-Radio project aims to enhance the in vivo stability of 211At-labeled radiopharmaceuticals by exploring alternative bonding methods, improving cancer treatment efficacy.

Subsidie
€ 2.357.165
2023

Projectdetails

Introduction

Astatine (At) is the rarest naturally occurring element on Earth, exhibiting only short-lived radioisotopes. One of them, 211At, decays with a half-life of 7.2 hours by emission of a highly energetic alpha particle, making it one of the rare alpha emitters suitable for targeted alpha therapy (TAT) of cancers, if bound to an appropriate cancer targeting molecule.

Accessibility of 211At

Because the number of cyclotrons able to produce it has seen a significant rise in the past years, it is expected that 211At will become more accessible and play a major role in the development of TAT.

Chemical Properties of Astatine

Astatine belongs to the halogen elements, and despite more than 80 years since its discovery, many chemical properties remain to be discovered. This lack of knowledge is due to the absence of stable isotopes and the availability in minute amounts that preclude the use of standard analytical methods.

Research has shown that At behaves similarly to metals but also to halogens, forming bonds similar to its closest homologue, iodine, such as the carbon-At bond. This strategy is the main approach currently available to develop 211At-labeled radiopharmaceuticals.

Challenges with C-At Bond

Yet, a lack of in vivo stability of the C-At bond is often observed, resulting in the release of 211At before it reaches its target and leading to irradiation of healthy tissues. Improving this stability is therefore a major challenge that remains to be overcome in order to unleash the potential of 211At in cancer treatments.

Project Objective

In this context, the objective of the SAt-Radio project is to explore alternative bonding modalities to the C-At bond in order to develop novel radiolabeling approaches with improved in vivo stability.

The strategies developed will exploit both the halogen and the metallic character of At, using analytical and computational approaches that have recently become available, making it possible to elucidate the chemistry of this enigmatic element at the trace concentration it is available.

Financiële details & Tijdlijn

Financiële details

Subsidiebedrag€ 2.357.165
Totale projectbegroting€ 2.357.165

Tijdlijn

Startdatum1-10-2023
Einddatum30-9-2028
Subsidiejaar2023

Partners & Locaties

Projectpartners

  • CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRSpenvoerder
  • NANTES UNIVERSITE

Land(en)

France

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