4.6 Article

15N Hyperpolarization by Reversible Exchange Using SABRE-SHEATH

期刊

JOURNAL OF PHYSICAL CHEMISTRY C
卷 119, 期 16, 页码 8786-8797

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.5b01799

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资金

  1. NSF [CHE-1058727, CHE-1363008, CHE-1416268]
  2. NIH [1R21EB018014, 1R21GM107947-02, 2R15EB007074]
  3. DOD CDMRP breast cancer award [W81XWH-12-1-0159/BC112431]
  4. Division Of Chemistry
  5. Direct For Mathematical & Physical Scien [1363008, 1416432, 1416268] Funding Source: National Science Foundation

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NMR signal amplification by reversible ex, change (SABRE) is a NMR hyperpolarization technique that enables nuclear spin polarization enhancement of molecules via concurrent chemical exchange of a target, substrate and parahydrogen (the source of spin order) on an iridium catalyst Recently, we demonstrated that conducting SABRE in microtesla fields provided by a magnetic Shield enables up to 10% N-15-polarization (Theis, T.; et al. J. Am. Chem. Soc. 2015, 137, 1404). Hyperpolarization on N-15 (and heteronuclei in general) may be advantageous because of the long-lived nature of the hyperpolarization on N-15 relative to the short-lived hyperpolarization of protons conventionally hyperpolarized by, SABRE, in addition to wider chemical. Shift dispersion and absence of background signal. Here we show that these unprecedented polarization levels enable N-15 magnetic resonance imaging. We also present a theoretical model for the hyperpolarization transfer to heteronuclei, and detail key parameters that should be optimized far efficient N-15-hyperpolarization. The effects of parahydrogen pressure, flow rate, sample temperature, catalyst-to-substrate:ratio, relaxation time (T-1), and reversible oxygen quenching are studied on a test System of N-15-pyridine In methanol-d(4) Moreover, we demonstrate the first proof-of-principle C-13-hyperpolarization using this method. This simple hyperpolarization scheme only requires access to parahydrogen: and a magnetic Shield, and it provides large enough signal gain's to enable one of the first N-15 images (2 x mm(2) resolution). Importantly) this method enables hyperpolarization of molecular sites with NMR T-1 relaxation times suitable for biomedical imaging and spectroscopy.

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