Hyperpolarized Nanodiamond with Long Spin Relaxation Times
Ewa Rej, Torsten Gaebel, Thomas Boele, David E. J. Waddington, and, David J. Reilly

TL;DR
This paper demonstrates that hyperpolarized 13C spins in synthetic nanodiamond can achieve long relaxation times exceeding one hour, enabling enhanced magnetic resonance imaging without toxic radicals.
Contribution
It introduces a method to hyperpolarize 13C in nanodiamond with relaxation times over an hour, surpassing previous short-lived agents and expanding theranostic applications.
Findings
13C in nanodiamond can be hyperpolarized at room temperature
Relaxation times exceed 1 hour in solid-state nanodiamond
No toxic free-radicals are needed for hyperpolarization
Abstract
The use of hyperpolarized agents in magnetic resonance (MR), such as 13C-labeled compounds, enables powerful new imaging and detection modalities that stem from a 10,000-fold boost in signal. A major challenge for the future of the hyperpolarizaton technique is the inherently short spin relaxation times, typically < 60 seconds for 13C liquid-state compounds, which limit the time that the signal remains boosted. Here, we demonstrate that 1.1% natural abundance 13C spins in synthetic nanodiamond (ND) can be hyperpolarized at cryogenic and room temperature without the use of toxic free- radicals, and, owing to their solid-state environment, exhibit relaxation times exceeding 1 hour. Combined with the already established applications of NDs in the life-sciences as inexpensive fluorescent markers and non-cytotoxic substrates for gene and drug delivery, these results extend the theranostic…
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