超极化(物理学)
化学
水溶液
生物分子
极化(电化学)
试剂
溶解
分子
组合化学
核磁共振波谱
有机化学
生物化学
物理化学
作者
Stephan Knecht,John W. Blanchard,Danila A. Barskiy,Eleonora Cavallari,Laurynas Dagys,Erik Van Dyke,Maksim Tsukanov,Bea Bliemel,Kerstin Münnemann,Silvio Aime,Francesca Reineri,Malcolm H. Levitt,Gerd Buntkowsky,Alexander Pines,Peter Blümler,Dmitry Budker,James Eills
标识
DOI:10.1073/pnas.2025383118
摘要
Hyperpolarized fumarate is a promising biosensor for carbon-13 magnetic resonance metabolic imaging. Such molecular imaging applications require nuclear hyperpolarization to attain sufficient signal strength. Dissolution dynamic nuclear polarization is the current state-of-the-art methodology for hyperpolarizing fumarate, but this is expensive and relatively slow. Alternatively, this important biomolecule can be hyperpolarized in a cheap and convenient manner using parahydrogen-induced polarization. However, this process requires a chemical reaction, and the resulting solutions are contaminated with the catalyst, unreacted reagents, and reaction side-product molecules, and are hence unsuitable for use in vivo. In this work we show that the hyperpolarized fumarate can be purified from these contaminants by acid precipitation as a pure solid, and later redissolved to a desired concentration in a clean aqueous solvent. Significant advances in the reaction conditions and reactor equipment allow for formation of hyperpolarized fumarate at 13C polarization levels of 30-45%.
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