{ "id": "1502.06214", "version": "v1", "published": "2015-02-22T11:08:09.000Z", "updated": "2015-02-22T11:08:09.000Z", "title": "Hyperpolarized Nanodiamond with Long Spin Relaxation Times", "authors": [ "Ewa Rej", "Torsten Gaebel", "Thomas Boele", "David E. J. Waddington", "David J. Reilly" ], "comment": "Supplemental Material available on request", "categories": [ "cond-mat.mes-hall", "quant-ph" ], "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 capabilities of nanoscale diamonds into the domain of hyperpolarized MR.", "revisions": [ { "version": "v1", "updated": "2015-02-22T11:08:09.000Z" } ], "analyses": { "keywords": [ "long spin relaxation times", "hyperpolarized nanodiamond", "inherently short spin relaxation times", "natural abundance 13c spins", "13c liquid-state compounds" ], "publication": { "doi": "10.1038/ncomms9459", "journal": "Nature Communications", "year": 2015, "month": "Oct", "volume": 6, "pages": 8459 }, "note": { "typesetting": "TeX", "pages": 0, "language": "en", "license": "arXiv", "status": "editable", "adsabs": "2015NatCo...6E8459R" } } }