Method for the generation of radicals for dynamic nuclear polarization and uses thereof for NMR, MRS and MRI

Patent metadata

Field	Value
Publication number	US-10114088-B2
Application number	US-201314775191-A
Country	US
Kind code	B2
Filing date	Mar 14, 2013
Priority date	Mar 14, 2013
Publication date	Oct 30, 2018
Grant date	Oct 30, 2018

Abstract

A method for the preparation of a sample comprising highly polarized nuclear spins is proposed, comprising at least the following steps:
a) provision of molecules with 1,2-dione structural units and/or molecules with 2,5-diene-1,4-dione structural units in the solid state; b) generation of radicals from these molecules by photo induced electron transfer by a first electromagnetic irradiation in the visible or ultraviolet frequency range in the solid state; c) dynamic nuclear polarization in the presence of a magnetic field in the solid state by applying a second electromagnetic irradiation with a frequency adapted to transfer spin polarization from the electrons to the nuclear spins leading to a highly polarized state thereof. Furthermore uses of correspondingly prepared samples for NMR, MRS and MRI experiments are proposed.

First claim

The invention claimed is:

1. A method for the preparation of a sample comprising highly polarized nuclear spins, comprising at least the following steps:
a) provision of molecules in a solid state selected from the group consisting of: molecules with 1,2-dione structural units, molecules with 2,5-diene-1,4-dione structural units, and combinations thereof;
b) generation of radicals from these molecules in the solid state by photo induced electron transfer by a first electromagnetic irradiation in the visible or ultraviolet frequency range;
c) dynamic nuclear polarization in the presence of a magnetic field in the solid state by applying a second electromagnetic irradiation with a frequency adapted to transfer spin polarization from electrons to the nuclear spins leading to a highly polarized state thereof.

2. The method according to claim 1 , wherein the first electromagnetic irradiation is applied with a frequency essentially equal to the difference or the sum of Larmor frequencies of the electron spins and the nuclear spins, respectively, in the presence of the applied magnetic field.

3. The method according to claim 1 , wherein the first and second electromagnetic irradiation in steps b) and c) are applied sequentially.

4. The method according to claim 3 , wherein for the first irradiation one, two or more light sources are used in pulsed mode operation forming trains of light pulses of different photon energies, different pulse intensities, different pulse lengths or combinations thereof, that either overlap or are separated in time in order to optically pump electronic transitions to reach a reactive molecular state.

5. The method according to claim 1 , wherein the molecules with 1,2-dione structural units are selected from the molecules according to formula (1):

or wherein the molecules with 2,5-diene-1,4-dione structural unit are selected from the molecules according to formula (2)

wherein in both cases, independently, R 1 and/or R 2 are selected to be a non-reactive group, and in both cases, independently, R 1 and/or R 2 are selected to be a reactive functional group allowing for a linking to biomolecules and/or a crosslinking of biomolecules of interest.

6. The method according to claim 5 , wherein the molecules are isotopically enriched.

7. The method according to claim 1 , wherein the molecules are selected from the group consisting of: diacetyl, 2,3-pentanedione, 2,3-hexanedione, 2,3-heptanedione, pyruvic acid, oxaloacetatic acid, alpha-keto isocaproate, alpha-ketoisovaleric acid, 3-mercaptopyruvic acid, 2-oxoglutaric acid, 2-ketobutyric acid, 2-ketohexanoic acid, 2-oxo-4-methylthiobutanoic acid, 2-ketopalmitic acid, dehydroascorbic acid, fumaric acid, maleic acid, adrenochrome, cholesterol derivatives with 2,5-diene-1,4-dione structural unit, Coenzyme Q10, dopamine homologues with 1,2 dione structural units, dopa homologues with 1,2 dione structural units, and derivatives thereof and mixtures thereof.

8. The method according to claim 1 , wherein the molecules or a mixture thereof are forming the sample for step a) entirely,
or wherein the molecules are provided as a solvent for further molecules, and then cooled to the solid state for steps b) and c),
or wherein the molecules are provided in another solvent, and then cooled to the solid state for steps b) and c).

9. The method according to claim 1 , wherein subsequent to step c) the sample is warmed up until reaching liquid state, and used for liquid or solid nuclear magnetic resonance (NMR) or both, magnetic resonance spectroscopy (MRS) or magnetic resonance imaging (MRI), including in vitro or in vivo.

10. The method according to claim 1 , wherein the molecules are peptides, proteins, or RNA or DNA comprising the structural units or with at least one structural unit attached either directly or via a spacer.

11. The method according to claim 1 , in which the sample is photo-excited with light outside within step b) in a DNP polarizer or a cryo-DNP magic angle spinning (MAS) probe prior to be transferred inside a DNP polarizer or a Cryo-DNP MAS probe for step c) that will be inserted inside an NMR magnet,
or in which the sample is photo-excited with the light inside a DNP polarizer
or in which the sample is photo-excited with light inside a Cryo-DNP MAS probe inserted inside an NMR magnet.

12. The method according to claim 1 in which the sample is exposed to acoustic waves or an electrical field prior to be warmed up after step c) in order to force a scavenging of the radicals.

13. The method according to claim 1 , wherein after step c) the sample is warmed up with a cold gas or a cold liquid to bring a temperature of a frozen solution between 77K and 273K in order to force a scavenging of the radicals while keeping the solution frozen,
or wherein the samples are extracted as a solid and melted outside a polarizer.

14. The method according to claim 1 , wherein the sample is dissolved outside a DNP polarizer in a solvent thermalized at a temperature above a melting temperature of the sample
or wherein the sample is dissolved inside the DNP polarizer in a solvent thermalized at a temperature above the melting temperature of the samples.

15. Nuclear magnetic resonance (NMR), magnetic resonance spectroscopy (MRS) or magnetic resonance imaging (MRI) experiment, including in vitro or in vivo, using a hyperpolarized sample prepared using a method according to claim 1 , for enhancing a signal-to-noise ratio.

16. The method according to claim 1 , wherein the first electromagnetic irradiation is applied with a frequency essentially equal to the difference or the sum of Larmor frequencies of electron spins and the nuclear spins, respectively, in the presence of the applied magnetic field, wherein the magnetic field is a static, essentially homogeneous magnetic field with a strength of at least 3 T.

17. The method according to claim 1 , wherein the first electromagnetic irradiation is applied with a frequency essentially equal to the difference or the sum of Larmor frequencies of electron spins and the nuclear spins, respectively, in the presence of the applied magnetic field, and wherein a temperature during the first or second electromagnetic irradiation or both is in the range of less than 120K.

18. The method according to claim 1 , wherein the first electromagnetic irradiation is applied with a frequency essentially equal to the difference or the sum of Larmor frequencies of electron spins and the nuclear spins, respectively, in the presence of the applied magnetic field, and wherein a temperature during the first or second electromagnetic irradiation or both, in the range of less than 5K.

19. The method according to claim 1 , wherein the first and second electromagnetic irradiation in steps b) and c) are applied sequentially, and wherein the first irradiation takes place in the absence of a magnetic field for at least 10 minutes.

20. The method according to claim 1 , wherein the first and second electromagnetic irradiation in steps b) and c) are applied sequentially, and wherein the first irradiation takes place in the absence of a magnetic field for in the range of 40-300 minutes.

21. The method according to claim 1 , wherein the first and second electromagnetic irradiation in steps b) and c) are applied sequentiall

Assignees

• Ecole Polytechnique Fed Lausanne Epfl

Inventors

• Eichhorn Tim Rolf
• Roussel Christophe
• Comment Arnaud

Classifications

• G01R33/62

  using double resonance (G01R33/24 takes precedence) · CPC title

• G01R33/282 Primary

  Means specially adapted for hyperpolarisation or for hyperpolarised contrast agents, e.g. for the generation of hyperpolarised gases using optical pumping cells, for storing hyperpolarised contrast agents or for the determination of the polarisation of a hyperpolarised contrast agent · CPC title

• G01R33/30 Primary

  Sample handling arrangements, e.g. sample cells, spinning mechanisms · CPC title

• G01R33/5601

  involving use of a contrast agent for contrast manipulation, e.g. a paramagnetic, super-paramagnetic, ferromagnetic or hyperpolarised contrast agent · CPC title

• G01R33/465

  applied to biological material, e.g. in vitro testing · CPC title