# Stable electron-irradiated [1-13C]alanine radicals for metabolic imaging with dynamic nuclear polarization

**Authors:** Catriona H. E. Rooney, Justin Y. C. Lau, Esben S. S. Hansen, Nichlas Vous Christensen, Duy A. Dang, Kristoffer Petersson, Iain D. C. Tullis, Borivoj Vojnovic, Sean Smart, William Myers, Zoe Richardson, Jarrod Lewis, Brett W. C. Kennedy, Alice M. Bowen, Lotte Bonde Bertelsen, Christoffer Laustsen, Damian J. Tyler, Jack J. Miller

PMC · DOI: 10.1126/sciadv.adz4334 · Science Advances · 2025-11-21

## TL;DR

Researchers developed a new method to create stable radicals for metabolic imaging using electron irradiation, which could improve magnetic resonance imaging sensitivity.

## Contribution

A novel mechanism for generating stable radicals using electron irradiation is proposed, enabling easier and safer metabolic imaging.

## Key findings

- Electron-irradiated alanine radicals are stable at room temperature and generate high nuclear polarization.
- The radicals quench upon dissolution and are suitable for in vivo metabolic imaging in rats.
- The process is sterilizing and avoids the need for cryogenic transport.

## Abstract

Dissolution dynamic nuclear polarization (dDNP) increases the sensitivity of magnetic resonance experiments by >104-fold, permitting isotopically labeled molecules to be transiently visible in magnetic resonance imaging scans. dDNP mechanistically takes place at ~1 K and requires unpaired electrons and microwaves. These electrons are usually chemical radicals, requiring removal by filtration prior to injection into humans. Alternative sources, such as ultraviolet irradiation, generate lower polarization and require cryogenic transport. We present ultrahigh–dose rate electron irradiation as an alternative for generating nonpersistent radicals in alanine/glycerol mixtures. These are stable for months at room temperature, quench spontaneously upon dissolution, are present in dose-dependent concentrations, and generate comparable nuclear polarization (17%) to trityl radicals used clinically (19%) through a previously unknown mechanism we believe to involve partial ordering and electron-electron interactions. Owing to the large radiation doses required, this process is sterilizing, permits imaging of alanine metabolism in vivo in the rat kidney, and may aid clinically translating dDNP.

Six-MeV electrons generate stable radicals for more accessible metabolic imaging with dDNP through a previously unknown mechanism.

## Linked entities

- **Chemicals:** alanine (PubChem CID 239), glycerol (PubChem CID 753)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Chemicals:** glycerol (MESH:D005990), [1-13C]alanine (-), alanine (MESH:D000409)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

140 references — full list in the complete paper: https://tomesphere.com/paper/PMC12637281/full.md

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Source: https://tomesphere.com/paper/PMC12637281