Photoinduced Nonpersistent Radicals as Polarizing Agents for X-Nuclei Dissolution Dynamic Nuclear Polarization

被引:33
作者
Capozzi, Andrea [1 ]
Hyacinthe, Jean-Noel [4 ,5 ]
Cheng, Tian [1 ]
Eichhorn, Tim R. [6 ]
Boero, Giovanni [2 ]
Roussel, Christophe [3 ]
van der Klink, Jacques J. [1 ]
Comment, Arnaud [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Inst Phys Biol Syst, CH-1015 Lausanne, Switzerland
[2] Ecole Polytech Fed Lausanne, Inst Microengn, CH-1015 Lausanne, Switzerland
[3] Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn, Sect Chem & Chem Engn, CH-1015 Lausanne, Switzerland
[4] Univ Appl Sci & Arts Western Switzerland HES SO, Sch Hlth Sci Geneva, Geneva, Switzerland
[5] Univ Geneva, Fac Med, Image Guided Intervent Lab, Geneva, Switzerland
[6] PSI, Sample Environm & Polarized Targets Grp, Villigen, Switzerland
基金
瑞士国家科学基金会;
关键词
DNP; PRINCIPLES; INJECTION; TIMES; BDPA;
D O I
10.1021/acs.jpcc.5b07315
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hyperpolarization via dissolution dynamic nuclear polarization (DNP) is a versatile method to dramatically enhance the liquid-state NMR signal of X-nuclei and can be used for performing metabolic and molecular imaging. It was recently demonstrated that instead of incorporating persistent radicals as source of unpaired electron spins, required for DNP, nonpersistent radicals can be photoinduced in frozen beads of neat pyruvic acid (PA), the most common substrate for metabolic imaging. In the present work, it is shown that the same radicals can be created in frozen solutions containing a fraction of PA in addition to C-13- or Li-6-labeled salts or Xe-129 nuclei. The use of these nonpersistent radicals prevents the loss of a substantial part of the polarization during the transfer of hyperpolarized solutions into iron-shielded high-field MRI scanners. It is also demonstrated that UV-irradiated d(4)-PA yields nonpersistent radicals exhibiting similarities with the most efficient and widely used persistent trityl radicals.
引用
收藏
页码:22632 / 22639
页数:8
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