Research output: Contribution to journal › Article › peer-review
Effects of Deuteration of 13C-Enriched Phospholactate on Efficiency of Parahydrogen-Induced Polarization by Magnetic Field Cycling. / Salnikov, Oleg G.; Shchepin, Roman V.; Chukanov, Nikita V. et al.
In: Journal of Physical Chemistry C, Vol. 122, No. 43, 01.11.2018, p. 24740-24749.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Effects of Deuteration of 13C-Enriched Phospholactate on Efficiency of Parahydrogen-Induced Polarization by Magnetic Field Cycling
AU - Salnikov, Oleg G.
AU - Shchepin, Roman V.
AU - Chukanov, Nikita V.
AU - Jaigirdar, Lamya
AU - Pham, Wellington
AU - Kovtunov, Kirill V.
AU - Koptyug, Igor V.
AU - Chekmenev, Eduard Y.
PY - 2018/11/1
Y1 - 2018/11/1
N2 - We report herein a large-scale (>10 g) synthesis of isotopically enriched 1-13C-phosphoenolpyruvate and 1-13C-phosphoenolpyruvate-d2 for application in hyperpolarized imaging technology. 1-13C-Phosphoenolpyruvate-d2 was synthesized with 57% overall yield (over two steps), and >98% 2H isotopic purity, representing an improvement over the previous report. The same outcome was achieved for 1-13C-phosphoenolpyruvate. These two unsaturated compounds with C=C bonds were employed for parahydrogen-induced polarization via pairwise parahydrogen addition in aqueous medium. We find that deuteration of 1-13C-phosphoenolpyruvate resulted in overall increase of 1H T1 of nascent hyperpolarized protons (4.30 ± 0.04 s versus 2.06 ± 0.01 s) and 1H polarization (∼2.5% versus ∼0.7%) of the resulting hyperpolarized 1-13C-phospholactate. The nuclear spin polarization of nascent parahydrogen-derived protons was transferred to 1-13C nucleus via a magnetic field cycling procedure. The proton T1 increase in deuterated hyperpolarized 1-13C-phospholactate yielded approximately 30% better 13C polarization compared to that of nondeuterated hyperpolarized 1-13C-phospholactate. Analysis of T1 relaxation revealed that deuteration of 1-13C-phospholactate may have resulted in approximately 3-fold worse 1H → 13C polarization transfer efficiency via magnetic field cycling. Since magnetic field cycling is a key polarization transfer step in the side-arm hydrogenation approach, the presented findings may guide more rational design of a broad range of 13C hyperpolarized contrast agents for molecular imaging employing 13C MRI. The hyperpolarized 1-13C-phospholactate-d2 is of biomedical imaging relevance because it undergoes in vivo dephosphorylation and becomes 13C hyperpolarized lactate, which as we show can be detected in the brain by 13C hyperpolarized MRI; this feasibility demonstration has implications for future imaging of neurodegenerative diseases and dementia.
AB - We report herein a large-scale (>10 g) synthesis of isotopically enriched 1-13C-phosphoenolpyruvate and 1-13C-phosphoenolpyruvate-d2 for application in hyperpolarized imaging technology. 1-13C-Phosphoenolpyruvate-d2 was synthesized with 57% overall yield (over two steps), and >98% 2H isotopic purity, representing an improvement over the previous report. The same outcome was achieved for 1-13C-phosphoenolpyruvate. These two unsaturated compounds with C=C bonds were employed for parahydrogen-induced polarization via pairwise parahydrogen addition in aqueous medium. We find that deuteration of 1-13C-phosphoenolpyruvate resulted in overall increase of 1H T1 of nascent hyperpolarized protons (4.30 ± 0.04 s versus 2.06 ± 0.01 s) and 1H polarization (∼2.5% versus ∼0.7%) of the resulting hyperpolarized 1-13C-phospholactate. The nuclear spin polarization of nascent parahydrogen-derived protons was transferred to 1-13C nucleus via a magnetic field cycling procedure. The proton T1 increase in deuterated hyperpolarized 1-13C-phospholactate yielded approximately 30% better 13C polarization compared to that of nondeuterated hyperpolarized 1-13C-phospholactate. Analysis of T1 relaxation revealed that deuteration of 1-13C-phospholactate may have resulted in approximately 3-fold worse 1H → 13C polarization transfer efficiency via magnetic field cycling. Since magnetic field cycling is a key polarization transfer step in the side-arm hydrogenation approach, the presented findings may guide more rational design of a broad range of 13C hyperpolarized contrast agents for molecular imaging employing 13C MRI. The hyperpolarized 1-13C-phospholactate-d2 is of biomedical imaging relevance because it undergoes in vivo dephosphorylation and becomes 13C hyperpolarized lactate, which as we show can be detected in the brain by 13C hyperpolarized MRI; this feasibility demonstration has implications for future imaging of neurodegenerative diseases and dementia.
KW - C-13 POLARIZATION
KW - HYDROGEN-INDUCED POLARIZATION
KW - HYPERPOLARIZED CONTRAST AGENTS
KW - IN-VIVO
KW - PASADENA HYPERPOLARIZATION
KW - PHIP
KW - PYRUVATE
KW - RESONANCE
KW - SPIN ORDER
KW - TRANSFORMATION
UR - http://www.scopus.com/inward/record.url?scp=85055350872&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.8b07365
DO - 10.1021/acs.jpcc.8b07365
M3 - Article
C2 - 31447960
AN - SCOPUS:85055350872
VL - 122
SP - 24740
EP - 24749
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
SN - 1932-7447
IS - 43
ER -
ID: 17233995