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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. и др.

в: Journal of Physical Chemistry C, Том 122, № 43, 01.11.2018, стр. 24740-24749.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Salnikov, OG, Shchepin, RV, Chukanov, NV, Jaigirdar, L, Pham, W, Kovtunov, KV, Koptyug, IV & Chekmenev, EY 2018, 'Effects of Deuteration of 13C-Enriched Phospholactate on Efficiency of Parahydrogen-Induced Polarization by Magnetic Field Cycling', Journal of Physical Chemistry C, Том. 122, № 43, стр. 24740-24749. https://doi.org/10.1021/acs.jpcc.8b07365

APA

Salnikov, O. G., Shchepin, R. V., Chukanov, N. V., Jaigirdar, L., Pham, W., Kovtunov, K. V., Koptyug, I. V., & Chekmenev, E. Y. (2018). Effects of Deuteration of 13C-Enriched Phospholactate on Efficiency of Parahydrogen-Induced Polarization by Magnetic Field Cycling. Journal of Physical Chemistry C, 122(43), 24740-24749. https://doi.org/10.1021/acs.jpcc.8b07365

Vancouver

Salnikov OG, Shchepin RV, Chukanov NV, Jaigirdar L, Pham W, Kovtunov KV и др. Effects of Deuteration of 13C-Enriched Phospholactate on Efficiency of Parahydrogen-Induced Polarization by Magnetic Field Cycling. Journal of Physical Chemistry C. 2018 нояб. 1;122(43):24740-24749. doi: 10.1021/acs.jpcc.8b07365

Author

Salnikov, Oleg G. ; Shchepin, Roman V. ; Chukanov, Nikita V. и др. / Effects of Deuteration of 13C-Enriched Phospholactate on Efficiency of Parahydrogen-Induced Polarization by Magnetic Field Cycling. в: Journal of Physical Chemistry C. 2018 ; Том 122, № 43. стр. 24740-24749.

BibTeX

@article{19d30e39ee4949a89534ef30e3f38063,
title = "Effects of Deuteration of 13C-Enriched Phospholactate on Efficiency of Parahydrogen-Induced Polarization by Magnetic Field Cycling",
abstract = "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.",
keywords = "C-13 POLARIZATION, HYDROGEN-INDUCED POLARIZATION, HYPERPOLARIZED CONTRAST AGENTS, IN-VIVO, PASADENA HYPERPOLARIZATION, PHIP, PYRUVATE, RESONANCE, SPIN ORDER, TRANSFORMATION",
author = "Salnikov, {Oleg G.} and Shchepin, {Roman V.} and Chukanov, {Nikita V.} and Lamya Jaigirdar and Wellington Pham and Kovtunov, {Kirill V.} and Koptyug, {Igor V.} and Chekmenev, {Eduard Y.}",
year = "2018",
month = nov,
day = "1",
doi = "10.1021/acs.jpcc.8b07365",
language = "English",
volume = "122",
pages = "24740--24749",
journal = "Journal of Physical Chemistry C",
issn = "1932-7447",
publisher = "American Chemical Society",
number = "43",

}

RIS

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