Hyperpolarized nanodiamond with long spin-relaxation times.
Hyperpolarized nanodiamond with long spin-relaxation times.
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DOI:
10.1038/ncomms9459
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发表时间:
2015-10-09
影响因子:
16.6
通讯作者:
Reilly DJ
中科院分区:
文献类型:
--
作者:
Rej E;Gaebel T;Boele T;Waddington DE;Reilly DJ
The use of hyperpolarized agents in magnetic resonance, such as 13C-labelled 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 hyperpolarization technique is the inherently short spin-relaxation times, typically <60 s 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 can be hyperpolarized at cryogenic and room temperature without the use of free radicals, and, owing to their solid-state environment, exhibit relaxation times exceeding 1 h. Combined with the already established applications of nanodiamonds in the life sciences as inexpensive fluorescent markers and non-cytotoxic substrates for gene and drug delivery, these results extend the theranostic capabilities of nanoscale diamonds into the domain of hyperpolarized magnetic resonance. Hyperpolarized carbon nuclei are promising contrast agents for magnetic resonance imaging, but typically possess relaxation times below one minute. Here, the authors demonstrate cryogenic and room temperature hyperpolarization of 13C in synthetic nanodiamonds with relaxation times exceeding one hour.