A system for magnetic detection includes a nitrogen vacancy (NV) diamond material, a radio frequency (RF) excitation source that provides RF excitation to the NV diamond material, an optical excitation source that provides optical excitation to the NV diamond material, an optical detector that receives an optical signal emitted by the NV diamond material, a magnetic field generator that generates a magnetic field applied to the NV diamond material, and a controller. The controller controls the RF excitation source to apply a first RF excitation having a first frequency and a second RF excitation having a second frequency. The first frequency is associated with a first slope point of a fluorescence intensity response of an NV center orientation of a first spin state, and the second frequency is associated with a second slope point of the fluorescence intensity response of the NV center orientation of the first spin state.

System and methods for determining an angle and/or geolocation of a dipole magnetic source relative to one or more DNV sensors. The system may include one or more DNV sensors, and a controller. The controller is configured to activate the DNV sensors, receive a set of vector measurements from the DNV sensors, and determine an angle of a magnetic source relative to the one or more DNV sensors based on the received set of vector measurements from the DNV sensors.

The invention pertains to advances in real-time methods in nuclear magnetic resonance by offering a new dual-frequency dynamic nuclear polarization (DNP) method that uses a microwave beam to polarize the spins of electrons and concomitantly act as a NMR transmitter.

The invention pertains to advances in real-time methods in nuclear magnetic resonance by offering a new dual-frequency dynamic nuclear polarization (DNP) method that uses a microwave beam to polarize the spins of electrons and concomitantly act as a NMR transmitter.

A system can include: a superconducting or permanent magnet; a high field portion corresponding to the superconducting or permanent magnet, wherein the high field has a range of 0.1-20 T; a low field portion positioned outside of the superconducting or permanent magnet, wherein the low field has a range of 0.01 nT-100 mT; a shuttling mechanism configured to deliver a sample between the low field portion and the high field portion; and a polarization sub-assembly configured to hyperpolarize the sample while the sample is within the low field portion. A device can be configured to cause nuclear spin hyperpolarization in diamond particles such that the hyperpolarization is transferable to at least one of an external liquid or an external solid. A process of hyperpolarizing substances can include applying optical illumination to the substance, irradiating the substance with a series of microwave signals as one of either a single signal or as a frequency comb to hyperpolarize the nuclei in the substance, and relaying polarization to nuclear spins of one of a surrounding solid or fluid.

Disclosed are methods for performing dynamic nuclear polarization using the polarizing agents described herein. In general, the methods involve (a) providing a frozen sample in a magnetic field, wherein the frozen sample includes a polarizing agent described herein and an analyte with at least one spin half nucleus; (b) polarizing the at least one spin half nucleus of the analyte by irradiating the frozen sample with radiation having a frequency that excites electron spin transitions in the polarizing agent; (c) optionally melting the sample to produce a molten sample; and (d) detecting nuclear spin transitions in the at least one spin half nucleus of the analyte in the frozen or molten sample. In certain embodiments, the polarizing agents can be peptide-based. In these embodiments, the polarizing agents can be readily prepared by solid-phase peptide synthesis.

Disclosed are methods for performing dynamic nuclear polarization using the polarizing agents described herein. In general, the methods involve (a) providing a frozen sample in a magnetic field, wherein the frozen sample includes a polarizing agent described herein and an analyte with at least one spin half nucleus; (b) polarizing the at least one spin half nucleus of the analyte by irradiating the frozen sample with radiation having a frequency that excites electron spin transitions in the polarizing agent; (c) optionally melting the sample to produce a molten sample; and (d) detecting nuclear spin transitions in the at least one spin half nucleus of the analyte in the frozen or molten sample. In certain embodiments, the polarizing agents can be peptide-based. In these embodiments, the polarizing agents can be readily prepared by solid-phase peptide synthesis.

The present invention relates to novel organic dinitroxide biradical compounds and their use as polarizing agents, in particular, in the techniques of Nuclear Magnetic Resonance (NMR) of solids or liquid samples and medical imaging.

The present application discloses a sensor system that includes a sensor having a sensor surface, a sample cartridge including one or more flexible membranes and a membrane frame, the membrane frame including one or more openings covered by the one or more flexible membranes defining one or more wells for holding one or more samples, the flexible membrane having a sample side supporting the sample and an opposite sensor side, the sample cartridge being removably insertable in the sensor system such that the sensor side of the flexible membrane is positioned above and faces the sensor surface, a displacement mechanism that can be actuated to displace the flexible membrane toward the sensor surface such that the sample is moved to a position closer to the sensor surface, and an optical imaging system that detects light emitted from the sensor. Disclosed also are a cartridge cassette and a method of use.

A method for obtaining an index for non-invasively identifying NASH is provided. A NASH determination method comprising a method for acquiring free radical consumption speed information by non-invasively detecting a redox reaction in a liver of a test animal in real time, comprises a step (1) of obtaining free radical concentration data by applying a magnetic resonance method to the liver as a measurement target after administering a probe into a body; a step (2) of obtaining imaging information by processing the obtained free radical concentration data; and a step (3) of obtaining a free radical consumption speed by kinetically measuring the imaging information over time, and comprises a step of determining whether or not the test animal has NASH, based on the free radical consumption speed information obtained through application to the test animal.