Department of Molecular Biotechnology and Health Sciences, University of Torino, Via Nizza 52, Turin, Italy.
Institute of Biostructures and Bioimaging, National Research Council, Via Nizza 52, Turin, Italy.
MAGMA. 2021 Feb;34(1):25-47. doi: 10.1007/s10334-020-00904-x. Epub 2021 Feb 2.
ParaHydrogen induced polarization (PHIP) is an efficient and cost-effective hyperpolarization method, but its application to biological investigations has been hampered, so far, due to chemical challenges. PHIP is obtained by means of the addition of hydrogen, enriched in the para-spin isomer, to an unsaturated substrate. Both hydrogen atoms must be transferred to the same substrate, in a pairwise manner, by a suitable hydrogenation catalyst; therefore, a de-hydrogenated precursor of the target molecule is necessary. This has strongly limited the number of parahydrogen polarized substrates. The non-hydrogenative approach brilliantly circumvents this central issue, but has not been translated to in-vivo yet. Recent advancements in hydrogenative PHIP (h-PHIP) considerably widened the possibility to hyperpolarize metabolites and, in this review, we will focus on substrates that have been obtained by means of this method and used in vivo. Attention will also be paid to the requirements that must be met and on the issues that have still to be tackled to obtain further improvements and to push PHIP substrates in biological applications.
反氢极化(ParaHydrogen induced polarization,PHIP)是一种高效且经济有效的极化方法,但由于化学方面的挑战,其在生物研究中的应用至今受到阻碍。PHIP 是通过向不饱和底物中添加富含反自旋异构体的氢来获得的。两个氢原子必须通过合适的氢化催化剂以成对的方式转移到同一底物上;因此,需要目标分子的脱氢前体。这强烈限制了可极化反氢的底物数量。非加氢方法巧妙地解决了这个核心问题,但尚未转化为体内应用。加氢 PHIP(h-PHIP)的最新进展极大地拓宽了使代谢物极化的可能性,在本综述中,我们将重点介绍通过这种方法获得并在体内使用的底物。我们还将关注必须满足的要求以及仍需解决的问题,以获得进一步的改进并推动 PHIP 底物在生物应用中的发展。