4.6 Article

Parahydrogen-Induced Polarization of Diethyl Ether Anesthetic

期刊

CHEMISTRY-A EUROPEAN JOURNAL
卷 26, 期 60, 页码 13621-13626

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.202002528

关键词

anesthetic; hydrogen; hyperpolarization; imaging agents; neurochemistry; parahydrogen

资金

  1. National Science Foundation [CHE-1904780]
  2. DOD CDMRP [W81XWH-15-1-0271]
  3. Russian Foundation for Basic Research [17-54-33037, 19-53-12013, 19-33-60045]
  4. Russian Ministry of Science and Higher Education [AAAA-A16-116121510087-5]
  5. Russian Science Foundation [19-13-00172]
  6. Russian Science Foundation [19-13-00172] Funding Source: Russian Science Foundation

向作者/读者索取更多资源

The growing interest in magnetic resonance imaging (MRI) for assessing regional lung function relies on the use of nuclear spin hyperpolarized gas as a contrast agent. The long gas-phase lifetimes of hyperpolarized(129)Xe make this inhalable contrast agent acceptable for clinical research today despite limitations such as high cost, low throughput of production and challenges of(129)Xe imaging on clinical MRI scanners, which are normally equipped with proton detection only. We report on low-cost and high-throughput preparation of proton-hyperpolarized diethyl ether, which can be potentially employed for pulmonary imaging with a nontoxic, simple, and sensitive overall strategy using proton detection commonly available on all clinical MRI scanners. Diethyl ether is hyperpolarized by pairwise parahydrogen addition to vinyl ethyl ether and characterized by(1)H NMR spectroscopy. Proton polarization levels exceeding 8 % are achieved at near complete chemical conversion within seconds, causing the activation of radio amplification by stimulated emission radiation (RASER) throughout detection. Although gas-phaseT(1)relaxation of hyperpolarized diethyl ether (at partial pressure of 0.5 bar) is very efficient, withT(1)of ca. 1.2 second, we demonstrate that, at low magnetic fields, the use of long-lived singlet states created via pairwise parahydrogen addition extends the relaxation decay by approximately threefold, paving the way to bioimaging applications and beyond.

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