Expeditious dissolution dynamic nuclear polarization without glassing agents

被引:18
|
作者
Lama, Bimala [1 ]
Collins, James H. P. [1 ]
Downes, Daniel [1 ]
Smith, Adam N. [2 ]
Long, Joanna R. [1 ]
机构
[1] Univ Florida, Dept Biochem & Mol Biol, Gainesville, FL 32610 USA
[2] Univ Florida, Dept Chem, Gainesville, FL 32610 USA
基金
美国国家科学基金会;
关键词
DNP; hyperpolarization; glassing agents; isopentane; C-13; MRS; toxicity; in vivo; vitrified; IN-VIVO; METABOLISM; STATE; MRI; CHEMISTRY; INCREASE; MATRIX; BRAIN; TIMES;
D O I
10.1002/nbm.3473
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The hyperpolarization of metabolic substrates at low temperature using dynamic nuclear polarization (DNP), followed by rapid dissolution and injection into an MRSI or NMR system, allows in vitro or in vivo observation and tracking of biochemical reactions and metabolites in real time. This article describes an elegant approach to sample preparation which is broadly applicable for the rapid polarization of aqueous small-molecule substrate solutions and obviates the need for glassing agents. We demonstrate its utility for solutions of sodium acetate, pyruvate and butyrate. The polarization behavior of substrates prepared using rapid freezing without glassing agents enabled a 1.5-3-fold time savings in polarization buildup, whilst removing the need for toxic glassing agents used as standard for dissolution DNP. The achievable polarization with fully aqueous substrate solutions was equal to that observed using standard approaches and glassing agents. Copyright (c) 2016 John Wiley & Sons, Ltd.
引用
收藏
页码:226 / 231
页数:6
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