A method for analyzing unconventional rock samples using nuclear magnetic resonance (NMR), tracking fluid change in the rock sample over a time period, calculating transverse relaxation time (T.sub.2) generating fluid distribution profiles by the computer processor and based on a NMR imaging, where the fluid distribution profiles representing a movement of the fluid, and obtaining, quantification of fracture volume by the computer processor and based on the NMR imaging.

A method for analyzing unconventional rock samples using nuclear magnetic resonance (NMR), tracking fluid change in the rock sample over a time period, calculating transverse relaxation time (T.sub.2) generating fluid distribution profiles by the computer processor and based on a NMR imaging, where the fluid distribution profiles representing a movement of the fluid, and obtaining, quantification of fracture volume by the computer processor and based on the NMR imaging.

The invention provides for a magnetic resonance imaging system (100) for acquiring magnetic resonance data (142) from a subject (118) within a measurement zone (108). The magnetic resonance imaging system (100) comprises: a processor (130) for controlling the magnetic resonance imaging system (100) and a memory (136) storing machine executable instructions (150, 152, 154), pulse sequence commands (140) and a dictionary (144). The pulse sequence commands (140) are configured for controlling the magnetic resonance imaging system (100) to acquire the magnetic resonance data (142) of multiple steady state free precession (SSFP) states per repetition time. The pulse sequence commands (140) are further configured for controlling the magnetic resonance imaging system (100) to acquire the magnetic resonance data (142) of the multiple steady state free precession (SSFP) states according to a magnetic resonance fingerprinting protocol. The dictionary (144) comprises a plurality of tissue parameter sets. Each tissue parameter set is assigned with signal evolution data pre-calculated for multiple SSFP states.

The invention provides for a magnetic resonance imaging system (100) for acquiring magnetic resonance data (142) from a subject (118) within a measurement zone (108). The magnetic resonance imaging system (100) comprises: a processor (130) for controlling the magnetic resonance imaging system (100) and a memory (136) storing machine executable instructions (150, 152, 154), pulse sequence commands (140) and a dictionary (144). The pulse sequence commands (140) are configured for controlling the magnetic resonance imaging system (100) to acquire the magnetic resonance data (142) of multiple steady state free precession (SSFP) states per repetition time. The pulse sequence commands (140) are further configured for controlling the magnetic resonance imaging system (100) to acquire the magnetic resonance data (142) of the multiple steady state free precession (SSFP) states according to a magnetic resonance fingerprinting protocol. The dictionary (144) comprises a plurality of tissue parameter sets. Each tissue parameter set is assigned with signal evolution data pre-calculated for multiple SSFP states.

The present patent disclosure relates to a method and a device 700 for determining a spatial distribution of at least one tissue parameter within a sample on a time domain magnetic resonance, TDMR, signal emitted from the sample after excitation of the sample according to an applied pulse sequence, a method of obtaining at least one time dependent parameter relating to a magnetic resonance, MR, signal emitted from a sample after excitation of the sample according to an applied spin echo pulse sequence, and a computer program product for performing the methods. A TDMR signal model is used to approximate the emitted time domain magnetic resonance signal. The model is factorized into one or more first matrix operators that have a non-linear dependence on the at least one tissue parameter and a remainder of the TDMR signal model.

The present patent disclosure relates to a method and a device 700 for determining a spatial distribution of at least one tissue parameter within a sample on a time domain magnetic resonance, TDMR, signal emitted from the sample after excitation of the sample according to an applied pulse sequence, a method of obtaining at least one time dependent parameter relating to a magnetic resonance, MR, signal emitted from a sample after excitation of the sample according to an applied spin echo pulse sequence, and a computer program product for performing the methods. A TDMR signal model is used to approximate the emitted time domain magnetic resonance signal. The model is factorized into one or more first matrix operators that have a non-linear dependence on the at least one tissue parameter and a remainder of the TDMR signal model.

The present application provides a system and method for using a nuclear magnetic resonance (NMR) system. The method includes performing a pulse sequence using the NMR system that spatially encodes NMR signal evolutions to be acquired from a subject using an aggregated radio-frequency (B1) field incoherence and resolving the NMR signal evolutions acquired from the subject using at least one of a dictionary of known magnetic resonance fingerprinting (MRF) signal evolutions to determine matches in the NMR signal evolutions to the known MRF signal evolutions or an optimization process. The method also includes generating at least two spatially-resolved measurements indicating quantitative tissue parameters of the subject in at least two locations.

In a method for measuring brain free water content, in response to an RF excitation field generated on the basis of a magnetic resonance fingerprinting sequence and applied to the brain, an equilibrium magnetization mixed term (M0) signal is acquired from radiation emitted by each excited voxel of the brain, to obtain an M0 value of each voxel of the brain; a receive coil sensitivity (RP) value of each voxel of the brain is acquired; the M0 value of each voxel of the brain is divided by the RP value of the corresponding voxel to obtain a proton density (PD) value of each voxel of the brain; a PD value of cerebrospinal fluid is taken to be a reference PD value; and the PD value of each voxel of the brain is divided by the reference PD value to obtain the free water content of each voxel of the brain. The method advantageously increases the speed and accuracy of measurement of brain free water content.

In a method for measuring brain free water content, in response to an RF excitation field generated on the basis of a magnetic resonance fingerprinting sequence and applied to the brain, an equilibrium magnetization mixed term (M0) signal is acquired from radiation emitted by each excited voxel of the brain, to obtain an M0 value of each voxel of the brain; a receive coil sensitivity (RP) value of each voxel of the brain is acquired; the M0 value of each voxel of the brain is divided by the RP value of the corresponding voxel to obtain a proton density (PD) value of each voxel of the brain; a PD value of cerebrospinal fluid is taken to be a reference PD value; and the PD value of each voxel of the brain is divided by the reference PD value to obtain the free water content of each voxel of the brain. The method advantageously increases the speed and accuracy of measurement of brain free water content.

Embodiments now disclosed herein provide an apparatus and method in which free radicals can be detected in a substance by MRI without changing the MRI static field.