WO2007124245A1 - Magnetic resonance with time sequential spin excitation - Google Patents

Magnetic resonance with time sequential spin excitation Download PDF

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Publication number
WO2007124245A1
WO2007124245A1 PCT/US2007/065841 US2007065841W WO2007124245A1 WO 2007124245 A1 WO2007124245 A1 WO 2007124245A1 US 2007065841 W US2007065841 W US 2007065841W WO 2007124245 A1 WO2007124245 A1 WO 2007124245A1
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WO
WIPO (PCT)
Prior art keywords
radio frequency
time
magnetic resonance
spatial
coil
Prior art date
Application number
PCT/US2007/065841
Other languages
French (fr)
Inventor
Zhiyong Zhai
Gordon D. Demeester
Michael A. Morich
Paul R. Harvey
Original Assignee
Koninklijke Philips Electronics, N.V.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Koninklijke Philips Electronics, N.V. filed Critical Koninklijke Philips Electronics, N.V.
Priority to EP07760008A priority Critical patent/EP2013636A1/en
Priority to JP2009506676A priority patent/JP5213849B2/en
Priority to US12/297,652 priority patent/US7852084B2/en
Publication of WO2007124245A1 publication Critical patent/WO2007124245A1/en

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Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01RMEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
    • G01R33/00Arrangements or instruments for measuring magnetic variables
    • G01R33/20Arrangements or instruments for measuring magnetic variables involving magnetic resonance
    • G01R33/44Arrangements or instruments for measuring magnetic variables involving magnetic resonance using nuclear magnetic resonance [NMR]
    • G01R33/48NMR imaging systems
    • G01R33/54Signal processing systems, e.g. using pulse sequences ; Generation or control of pulse sequences; Operator console
    • G01R33/56Image enhancement or correction, e.g. subtraction or averaging techniques, e.g. improvement of signal-to-noise ratio and resolution
    • G01R33/565Correction of image distortions, e.g. due to magnetic field inhomogeneities
    • G01R33/5659Correction of image distortions, e.g. due to magnetic field inhomogeneities caused by a distortion of the RF magnetic field, e.g. spatial inhomogeneities of the RF magnetic field
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01RMEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
    • G01R33/00Arrangements or instruments for measuring magnetic variables
    • G01R33/20Arrangements or instruments for measuring magnetic variables involving magnetic resonance
    • G01R33/28Details of apparatus provided for in groups G01R33/44 - G01R33/64
    • G01R33/32Excitation or detection systems, e.g. using radio frequency signals
    • G01R33/34Constructional details, e.g. resonators, specially adapted to MR
    • G01R33/341Constructional details, e.g. resonators, specially adapted to MR comprising surface coils
    • G01R33/3415Constructional details, e.g. resonators, specially adapted to MR comprising surface coils comprising arrays of sub-coils, i.e. phased-array coils with flexible receiver channels
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01RMEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
    • G01R33/00Arrangements or instruments for measuring magnetic variables
    • G01R33/20Arrangements or instruments for measuring magnetic variables involving magnetic resonance
    • G01R33/24Arrangements or instruments for measuring magnetic variables involving magnetic resonance for measuring direction or magnitude of magnetic fields or magnetic flux
    • G01R33/246Spatial mapping of the RF magnetic field B1

Definitions

  • the present application relates to the magnetic resonance arts. It particularly relates to reducing spatial non-uniformity in magnetic resonance applications due to coil Bi non-uniformity at ultra high field due to dielectric and conductivity effects by a subject, and is described with particular reference thereto.
  • the following relates more generally to reducing spatial non-uniformity in magnetic resonance applications generally, such as due to coil loading, equipment imperfections, static (Bo) magnetic field non-uniformity, dielectric or eddy current effects, or so forth.
  • Radio frequency coils for use in magnetic resonance scanners are typically configured to produce a substantially uniform Bi field within an examination region in the unloaded condition. That is, the radio frequency coil produces a substantially uniform Bi field without a subject arranged in the examination region. Ideally, a subject placed in the examination region will therefore experience a substantially spatially uniform Bi field that defines a substantially spatially uniform tip angle distribution of the spins throughout the subject, which is conducive to accurate magnetic resonance imaging and/or spectroscopy.
  • an object such as a human imaging subject
  • the insertion of an object, such as a human imaging subject, into the examination region can distort the B
  • Such distortions are typically due to dielectric and/or conductivity effects, and are related to the RF wavelength in the object becoming comparable to the size of the object.
  • Subject-induced Bj field distortion and loading becomes increasingly problematic as the asymmetry of the imaging subject increases (e.g., in the case of a "broad-shouldered" or otherwise asymmetric human imaging subject) and as the strength of the static (i.e., Bo) magnetic field increases.
  • Quadrature body coils provide efficient radio frequency coupling with a large region of interest such as a torso, legs, or other portion of a human imaging subject.
  • a quadrature body coil is generally cylindrical in shape, and has radial symmetry.
  • Examples include a quadrature birdcage body coil and a quadrature transverse-electromagnetic (TEM) body coil.
  • the quadrature body coil includes I and Q channel input ports that are driven by radio frequency energy at a 9Oo phase difference to produce a rotating Bs field for exciting magnetic resonance.
  • B] non-uniformity has been addressed in various ways.
  • the acquired magnetic resonance data is corrected after acquisition to account for distortion of the Bi field. While a correction for the receive coil sensitivity pattern can be made the excitation still has a distribution of tip angles that affects the MR experiment.
  • the range of excited tip angles can be reduced by using adiabatic RF pulses but this approach is time and RF exposure expensive as well a limiting RF sequences.
  • each of the I and Q ports may be driven by a different amplifier.
  • the amplitude and phase of each amplifier are selected to tailor the Bi field distribution.
  • the radio frequency coil can be reconfigured to include additional ports that are connected with additional radio frequency amplifiers.
  • a TEM coil can be configured to have each rung, or each selected group of rungs, independently driven by a different radio frequency amplifier.
  • a magnetic resonance scanner is disclosed.
  • a main magnet generates a static magnetic field at least in an examination region.
  • a magnetic resonance excitation system includes at least one radio frequency coil arranged to inject radio frequency energy into the examination region and at least two radio frequency amplifiers coupled with different input ports of the at least one radio frequency coil.
  • a controller controls the magnetic resonance excitation system to produce a time-varying spatial B i field distribution in a subject in the examination region that time-integrates to define a spatial tip angle distribution in the subject having reduced spatial non-uniformity.
  • a magnetic resonance excitation method is disclosed.
  • a B[ non-uniformity imposed on at least one radio frequency coil by a subject coupled with the at least one radio frequency coil is determined.
  • a time-varying spatial Bi field distribution is generated in the subject using the at least one radio frequency coil.
  • the time- varying spatial B] field distribution time-integrates to define a spatial tip angle distribution in the subject that is more spatially uniform than the time-varying spatial Bi field distribution.
  • a magnetic resonance excitation apparatus is disclosed. Means are provided for determining a B[ non-uniformity imposed on at least one radio frequency coil by a subject coupled with the at least one radio frequency coil. Means including the at least one radio frequency coil are provided for generating a time-varying spatial B 1 field distribution in the subject. The time-varying spatial Bi field distribution time-integrates to define a spatial tip angle distribution in the subject having reduced spatial non-uniformity.
  • One advantage resides in providing flexible and effective compensation for B] field non-uniformity.
  • Another advantage resides in providing compensation for different types of patterns of Bs non-uniformity without using different compensation coils or other loading-specific hardware.
  • Another advantage resides in acquisition of more accurate magnetic resonance data with reduced effects of Bi non-uniformity.
  • Another advantage resides in improved reconstructed image quality. Another advantage resides in improved magnetic resonance spectra. Still further advantages of the present invention will be appreciated to those of ordinary skill in the art upon reading and understand the following detailed description.
  • the invention may take form in various components and arrangements of components, and in various steps and arrangements of steps.
  • the drawings are only for purposes of illustrating the preferred embodiments and are not to be construed as limiting the invention.
  • FIGURE 1 diagrammatically shows a magnetic resonance scanner including a quadrature body coil, two independent radio frequency amplifiers separately driving the I and Q input ports of the quadrature body coil, and a two channel scanner controller with temporal sequencer for exciting a time-varying spatial B
  • FIGURE 2 diagrammatically shows the magnetic resonance excitation system of the magnetic resonance scanner of FIGURE 1 in greater detail.
  • FIGURE 3 show spatial Bi field distributions for modeling of an elliptical cardiac phantom placed in a quadrature body coil in a 3 Tesla magnetic field, for four different excitation conditions.
  • FIGURES 4 and 5 show spatial tip angle distributions produced by two different time-invariant Bi field distributions.
  • FIGURE 6 shows a spatial tip angle distribution for a time-integrated combination of the time-invariant Bi field distributions of FIGURES 4 and 5.
  • FIGURE 7 diagrammatically shows another magnetic resonance scanner employing a plurality of local coils in place of the quadrature body coil of FIGURE 1.
  • FIGURE 8 diagrammatically shows the magnetic resonance excitation system of the magnetic resonance scanner of FIGURE 7 in greater detail.
  • a magnetic resonance scanner 10 includes a scanner housing 12 in which a patient 16 or other subject is at least partially disposed.
  • a protective insulating bore liner 18 of the scanner housing 12 optionally lines a generally cylindrical bore or opening of the scanner housing 12 inside of which the subject 16 is disposed.
  • a main magnet 20 disposed in the scanner housing 12 is controlled by a main magnet controller 22 to generate a static (Bo) magnetic field in at least a scanning region including at least a portion of the subject 16.
  • the main magnet 20 is a persistent superconducting magnet surrounded by cryoshrouding 24.
  • the main magnet 20 generates a main magnetic field of at least about 0.2 Tesla, such as 0.23 Tesla, 1.5 Tesla, 3 Tesla, 7 Tesla, or so forth.
  • Magnetic field gradient coils 28 are arranged in or on the housing 12 to superimpose selected magnetic field gradients on the main magnetic field in at least the scanning region.
  • the magnetic field gradient coils include coils for producing three orthogonal magnetic field gradients, such as x-gradient, y-gradient, and z-gradient.
  • a generally cylindrical quadrature body coil 30 is mounted substantially coaxially with the bore of the magnetic resonance scanner 10.
  • the quadrature body coil 30 is a permanent fixture mounted inside the scanner housing 12.
  • the quadrature body coil 30 is mounted on a dielectric former or other holder that can be slidably inserted into and removed from the bore of the magnetic resonance scanner 10, or slidably inserted into and removed from an annular receptacle of the scanner housing 12.
  • the quadrature coil 30 can be a local quadrature coil, such as a head quadrature coil or a knee quadrature coil.
  • the quadrature body coil 30 is a quadrature birdcage coil including a plurality of rungs arranged generally parallel with the axis of the bore and operatively interconnected by two or more endrings, endcaps, or other terminating structures disposed at or near the opposite ends of the rungs.
  • the quadrature body coil 30 is a quadrature transverse-electromagnetic (TEM) coil including a plurality of rods arranged generally parallel with the axis of the bore and operatively interconnected by a generally annular radio frequency shield or screen substantially surrounding the rods.
  • the quadrature body coil 30 optionally includes capacitances, inductances, resistances, chokes, transistors, relays, or other components for providing radio frequency tuning, decoupling, current blocking or trapping, or other functionality.
  • the quadrature body coil 30 performs both transmit and receive functions. That is, the quadrature body coil 30 is externally energized to excite magnetic resonance in the subject 16, and is also used to receive magnetic resonance signals generated by the excitation. In some embodiments, the quadrature body coil 30 performs the transmit function, and a separate receive coil 34 receives magnetic resonance signals generated by the excitation.
  • the optional separate receive coil 34 can be a surface coil as illustrated, or a surface coils array, or an arm coil, leg coil, or other local coil.
  • the scanner 10 is configurable so that in some imaging applications the quadrature body coil 30 performs both transmit and receive functions while in other imaging applications the quadrature body coil 30 performs the transmit function and a separate receive coil performs the receive function.
  • the optional separate receive coil 34 typically includes detuning circuitry that detunes the receive coil during the transmit phase to avoid overloading the receive coil.
  • FIGURE 2 which shows a magnetic resonance excitation system 36 of the magnetic resonance scanner of FIGURE 1 in greater detail, an I-channel radio frequency amplifier
  • the I-channel and Q-channel radio frequency drive signals are independent in that they may have different amplitudes Ai, A Q (within the limits imposed by the dynamic ranges of the amplifiers 38, 40) and different relative phases ⁇ i, ⁇ Q .
  • the Q-channel drive signal output by the Q-channel radio frequency amplifier 40 is fed into a Q-channel input port 44 of the quadrature body coil 30.
  • the quadrature body coil 30 is operated in the usual quadrature mode that produces a B] field vector that rotates at the magnetic resonance frequency.
  • the quadrature body coil 30 is operated in the usual quadrature mode that produces a B] field vector that rotates at the magnetic resonance frequency.
  • two separate RF waveform generators and two independent amplifiers 38, 40 are provided, there is in general no restriction on the I- and Q-channel radio frequency drive signal amplitudes Aj, A Q and the phase difference ⁇ Q - ⁇ I therebetween.
  • a magnetic field gradients controller 54 operates the magnetic field gradient coils 28 to spatially localize the magnetic resonance excitation to a slab or other localized region.
  • the magnetic field gradient controller 54 operates the magnetic field gradient coils 28 to apply one or more spatial encoding magnetic field gradient pulses.
  • a radio frequency receiver 56 is operatively connected with the illustrated local coil 34 to read magnetic resonance signals during a readout phase of the magnetic resonance sequence.
  • the radio frequency receiver 56 is operatively coupled with the I and Q channel input ports 42, 44 of the quadrature body coil 30 during the readout phase, with suitably radio frequency circuitry being provided to switch between operative connection of the quadrature body coil 30 with the radio frequency amplifiers 38, 40 during the transmit phase and operative connection with the radio frequency receiver 56 during the readout phase.
  • the magnetic field gradient controller 54 operates the magnetic field gradient coils 28 during the readout phase to provide additional spatial encoding (i.e., readout encoding) of the magnetic resonance signals.
  • the magnetic resonance samples acquired during the readout are stored in a data buffer 58.
  • a magnetic resonance data processor 60 performs processing of the acquired magnetic resonance data to extract useful information.
  • the data processor 60 suitably performs image reconstruction using a Fast Fourier transform or other image reconstruction algorithms comporting with the selected spatial encoding applied during generation of the magnetic resonance data.
  • the processing performed by the data processor 60 may include, for example, performing spectral fast Fourier transform operations to recover chemical shift and J-coupling data.
  • the resulting processed data (e.g., images, spectra, or so forth) are suitably stored in a data/images memory 62, displayed on a user interface 64, printed, communicated over the Internet or a local area network, stored on a non-volatile storage medium, or otherwise used.
  • the user interface 64 also interfaces a radiologist or other operator with the scanner controller 66 to control the magnetic resonance scanner 10.
  • a separate scanner control interface may be provided.
  • the magnetic resonance excitation system 36 is configured to allow time-averaging of a B ⁇ (r) field so as to compensate for Bi spatial non-uniformity.
  • r denotes spatial position
  • B 1 (T) denotes the spatial B
  • Applying a time-invariant B ] (F) field for a time ⁇ produces a spatial tip angle distribution ⁇ (F) given by:
  • Equation (1) simplifies to:
  • ⁇ (F)
  • the magnetic resonance scanner 10 includes the capability of generating a time-varying spatial B x (F) field distribution that varies in spatial shape, by independently controlling the 1 and Q channel radio frequency amplifiers 38, 40. Denoting the time-varying spatial 2J 1 (F) field distribution as B x (F J) where t denotes time, Equation (1 ) becomes:
  • the time-varying spatial B x (Fj) field distribution could only be varied in amplitude or phase - that is, the spatial shape of the spatial B x (F, t) field distribution could not be varied. This is the case with a typical MR system.
  • the time-varying spatial B x (Fj) field distribution can have varying shape.
  • -field intensity are shown with whiter grayscale values; whereas, regions of low or high JBi + - field intensity are shown with darker grayscale values. That is, relatively uniform regions arc whiter, while regions substantially contributing to non-uniformity are darker. Substantial spatial non-uniformities are seen for each of the coil operational modes, principally due to dielectric and eddy current effects in the cardiac phantom.
  • a time-varying spatial Bi field distribution can be produced in a subject that time-integrates to define a spatial tip angle distribution in the subject having reduced spatial non-uniformity.
  • the combination can be continuous, e.g. by applying Equation (3), or can involve combining two or more time-invariant spatial Bi field distributions each held constant over selected time interval ⁇ .
  • the amplifiers 38, 40 can be controlled by the controller 66 to produce a first time-invariant spatial Bi field distribution B i (r
  • Equation (2) time ⁇ 2 , the first and second time-invariant spatial Bi field distributions being different due to different RF excitation conditions.
  • the combined tip angle Q (F) is given by a linear combination of Equation (2):
  • ⁇ (r)
  • FIGURES 4-6 show an application of Equation (4).
  • FIGURE 4 shows a spatial tip angle distribution B 1 (V) produced by a time-invariant B ⁇ (r) field
  • FIGURE 5 shows a spatial tip angle distribution G 2 (F) produced by a time-invariant
  • the central region represents a large tip angle of about 90-120°, while in the spatial tip angle distribution ⁇ 2 (r) of FIGURE 5, the central region represents a small tip angle of about 0-40°.
  • FIGURE 6 shows a spatial tip angle distribution ⁇ (F) for the time-integrated combination of the time-invariant p/ (r) and
  • FIGURE 6 shows a combination of two different time-invariant Bi field distributions B ⁇ (F) and B 1 (/-) , it is anticipated that by selectively combining three
  • W (2) different time-invariant Bi field distributions in accordance with Equation (5), or four or more different time-invariant Bi field distributions in accordance with Equation (6), can provide still further reduced spatial nonuniformity in the spatial tip angle distribution ⁇ (F) .
  • a time- varying spatial Bi field distribution can be chosen to produce a spatial tip angle distribution that is more spatially uniform than the time- varying spatial B, field distribution.
  • the time-invariant spatial Bi field distribution used to create a more uniform spatial tip angle distribution can be either continuously varying (analyzed using Equation (3)) or discretely varying (analyzed using Equations (4)-(6)).
  • the controller 66 controls the radio frequency amplifiers 38, 40 to generate output radio frequency signals with amplitudes A](t), A Q (t) and phases ⁇ [(t), ⁇ Q (t) that are functions of time to produce a time-varying field distribution Bf (r,t) that time-integrates in accordance with Equation (3) to produce a spatial tip angle distribution ⁇ (r) having reduced spatial non-uniformity.
  • the controller 66 controls the radio frequency amplifiers 38, 40 to generate a temporal sequence of time-invariant output radio frequency signals each having amplitudes A t (,,), AQ ⁇ J and phases ⁇ i(,, ) , ⁇ Q( ,, ) that produce time-invariant field distributions B ] (r) that sum in accordance with Equation (6) to produce a spatial tip
  • a temporal sequencer 70 determines suitable continuous functions A s (t), A Q (t), ⁇ j(t), ⁇ o(t) or discrete values A] (n) , A Q(H) , ⁇ ]( n) , ⁇ Q( ,, ) that provide the spatial tip angle distribution ⁇ (r) having reduced spatial non-uniformity based on a determination of the coil loading imposed on the radio frequency coil 30 by a subject in the examination region.
  • non-uniformity can be done in various ways.
  • a pre-scan is performed and an image of the subject reconstructed, and the B] non-uniformity estimated from the reconstructed image.
  • the B 1 non-uniformity may be estimated based on measurements of the dimensions of the subject. For example, the shoulder width and chest diameter of a human subject may be measured to estimate the amount of Bi non-uniformity the human subject will impose upon the coil.
  • the temporal sequencer 70 includes a look-up table of continuous functions A
  • the look-up table values arc suitably pre-determined by finite element analysis simulations, or by experimental measurements on phantoms or human objects with different aspect ratios, or so forth.
  • the temporal sequencer 70 may include a finite element analysis electromagnetic simulator or other calculator for estimating suitable values of the continuous functions A[(t), A Q (I), ⁇ i(t), ⁇ Q (1) or discrete values A[( n) , AQ ⁇ ), ⁇ i( n ), ⁇ QOU that provide substantial uniformity for the spatial tip angle distribution ⁇ (F) . That is, in the discrete embodiment a composite Bi pulse or pulse packet is applied by the amplifiers 38, 40 which includes a series of two (Equation (4)), three (Equation (5)), or N (Equation (6)) sub-pulses which cumulatively produce the selected spatial tip angle distribution.
  • Each sub-pulse has a selectable amplitude, phase, and/or duration to provide numerous degrees of freedom in tailoring the overall Bi pulse or pulse packet.
  • a sensor, sensor array or analyzer detects or measures the Bi field distribution to provide feedback 72 of the actual applied Bi field at the region of interest.
  • pulses are suitably applied and the detected or measured Bi field distribution is used by the temporal sequencer 70 to dynamically or iteratively adjust the Bj sub-pulses or Bj pulse shape to achieve the desired spatial tip angle distribution.
  • a dedicated sensor, sensor array or analyzer can be used, or the receive coil 34 can be used as the sensor, along with suitable processing performed by the data processor 60 or another processor, to produce the feedback 72 for dynamically or iteratively tailoring the Bi sub-pulses or Bi pulse shapes.
  • Equations (3)-(6)) to define a spatial tip angle distribution in the subject that is more spatially uniform than the time-varying spatial B] field distribution can be applied to other magnetic resonance excitation systems.
  • a magnetic resonance scanner 10' includes a different magnetic resonance excitation system 36' in which the quadrature body coil 30 is replaced by an array of local coils 301, 302, 303. While three local surface coils 301, 302, 303 are shown, other types and/or numbers of local coils can be used.
  • the I-channel and Q-channel radio frequency amplifiers 38, 40 are replaced by a set of three radio frequency amplifiers 40' that are independently controlled by the scanner controller 66.
  • each local coil 301, 302, 303 has an input port that is coupled to its own independent amplifier - accordingly, the local coil 301 can be operated at amplitude Ai(t) and phase ⁇ i(t), the local coil 302 can be operated at amplitude A 2 (t) and phase ⁇ 2 (t), and the local coil 303 can be operated at amplitude A 3 (t) and phase ⁇ 3 (t).
  • the local coils 301, 302, 303 operate as transmit/receive CTVR x ) coils that are selectively coupled with either the radio frequency amplifiers 40' or the radio frequency receiver 56 by a suitable switch 80.
  • the time-varying Bi field distribution ⁇ , + (r,f) is generated by the combination of local coils 301, 302, 303 based on the time-varying amplitudes Ai(t), A 2 (t), A 3 (t) and time-varying phases ⁇ s(t), ⁇ 2 (t), ⁇ 3 (t).
  • the time integration can be either continuous (where A ⁇ (t), A 2 (t), A 3 (t), ⁇ i(t), ⁇ 2 (t), ⁇ 3 (t) are in general continuous functions of time) or discrete (where the amplitudes and phases are varied discretely, e.g.
  • the example magnetic resonance excitation systems 36, 36' are not exhaustive.
  • a degenerate birdcage or TEM coil can be used, with individual rungs or rods driven by separate radio frequency amplifiers in accordance with the techniques disclosed herein.

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Abstract

In a magnetic resonance scanner, a main magnet (20, 22) generates a static magnetic field at least in an examination region. A magnetic field gradient system (30, 54) selectively superimposes magnetic field gradients on the static magnetic field at least in the examination region. A magnetic resonance excitation system (36, 36') includes at least one radio frequency coil (30, 301, 302, 303) arranged to inject radio frequency B1 fields into the examination region and at least two radio frequency amplifiers (38, 40, 40') coupled with different input ports of the at least one radio frequency coil. A controller (66, 70) controls the magnetic resonance excitation system to produce a time varying spatial B1 field distribution in a subject (16) in the examination region that time integrates to define a spatial tip angle distribution in the subject having reduced spatial non uniformity.

Description

MAGNETIC RESONANCE WITH TIME SEQUENTIAL SPIN EXCITATION
DESCRIPTION
The present application relates to the magnetic resonance arts. It particularly relates to reducing spatial non-uniformity in magnetic resonance applications due to coil Bi non-uniformity at ultra high field due to dielectric and conductivity effects by a subject, and is described with particular reference thereto. The following relates more generally to reducing spatial non-uniformity in magnetic resonance applications generally, such as due to coil loading, equipment imperfections, static (Bo) magnetic field non-uniformity, dielectric or eddy current effects, or so forth.
Radio frequency coils for use in magnetic resonance scanners are typically configured to produce a substantially uniform Bi field within an examination region in the unloaded condition. That is, the radio frequency coil produces a substantially uniform Bi field without a subject arranged in the examination region. Ideally, a subject placed in the examination region will therefore experience a substantially spatially uniform Bi field that defines a substantially spatially uniform tip angle distribution of the spins throughout the subject, which is conducive to accurate magnetic resonance imaging and/or spectroscopy.
However, the insertion of an object, such as a human imaging subject, into the examination region can distort the B| field, especially at Bo fields of 3T or higher. Such distortions are typically due to dielectric and/or conductivity effects, and are related to the RF wavelength in the object becoming comparable to the size of the object. Subject-induced Bj field distortion and loading, becomes increasingly problematic as the asymmetry of the imaging subject increases (e.g., in the case of a "broad-shouldered" or otherwise asymmetric human imaging subject) and as the strength of the static (i.e., Bo) magnetic field increases. Hence, coil loading has become increasingly problematic as commercial magnetic resonance scanners have progressed from low-field (e.g., 0.23 Tesla, 1.5 Tesla) to progressively higher static magnetic fields (e.g., 3 Tesla, 7 Tesla, or so forth). Loading the coil can also be more problematic for large coils that couple to a large examination region, both because of the larger subject size and the larger area over which a substantially uniform B| field is to be maintained. For large- volume imaging of human subjects, a quadrature body coil is sometimes used. Quadrature body coils provide efficient radio frequency coupling with a large region of interest such as a torso, legs, or other portion of a human imaging subject. A quadrature body coil is generally cylindrical in shape, and has radial symmetry. Examples include a quadrature birdcage body coil and a quadrature transverse-electromagnetic (TEM) body coil. The quadrature body coil includes I and Q channel input ports that are driven by radio frequency energy at a 9Oo phase difference to produce a rotating Bs field for exciting magnetic resonance. B] non-uniformity has been addressed in various ways. In a post-acquisition processing approach, the acquired magnetic resonance data is corrected after acquisition to account for distortion of the Bi field. While a correction for the receive coil sensitivity pattern can be made the excitation still has a distribution of tip angles that affects the MR experiment. The range of excited tip angles can be reduced by using adiabatic RF pulses but this approach is time and RF exposure expensive as well a limiting RF sequences.
In another approach, multiple independent radio frequency amplifiers arc used to generate a custom Bi field. For example, in the case of a quadrature body coil, each of the I and Q ports may be driven by a different amplifier. The amplitude and phase of each amplifier are selected to tailor the Bi field distribution. This approach works well, except that the extent of Bi field distribution tailoring is limited to four degrees of freedom, namely the amplitude and phase of each of the two amplifiers. To provide additional degrees of freedom, the radio frequency coil can be reconfigured to include additional ports that are connected with additional radio frequency amplifiers. For example, a TEM coil can be configured to have each rung, or each selected group of rungs, independently driven by a different radio frequency amplifier. For an eight clement TEM coil, for example, up to eight amplifiers can be used providing sixteen degrees of freedom for tailoring the Bj field. The substantial flexibility in tailoring the Bi field to compensate for coil loading using these approaches comes, however, at the cost of substantial increase in system complexity and cost. Radio frequency amplifiers are costly components. Each separately driven port requires its own waveform generation control, amplifier, and dedicated radio frequency cabling, trapping, and so forth. The additional radio frequency connections occupy valuable bore space and introduces opportunities for detrimental radio frequency cross -coupling. In accordance with one aspect, a magnetic resonance scanner is disclosed. A main magnet generates a static magnetic field at least in an examination region. A magnetic resonance excitation system includes at least one radio frequency coil arranged to inject radio frequency energy into the examination region and at least two radio frequency amplifiers coupled with different input ports of the at least one radio frequency coil. A controller controls the magnetic resonance excitation system to produce a time-varying spatial B i field distribution in a subject in the examination region that time-integrates to define a spatial tip angle distribution in the subject having reduced spatial non-uniformity. In accordance with another aspect, a magnetic resonance excitation method is disclosed. A B[ non-uniformity imposed on at least one radio frequency coil by a subject coupled with the at least one radio frequency coil is determined. A time-varying spatial Bi field distribution is generated in the subject using the at least one radio frequency coil. The time- varying spatial B] field distribution time-integrates to define a spatial tip angle distribution in the subject that is more spatially uniform than the time-varying spatial Bi field distribution.
In accordance with another aspect, a magnetic resonance excitation apparatus is disclosed. Means are provided for determining a B[ non-uniformity imposed on at least one radio frequency coil by a subject coupled with the at least one radio frequency coil. Means including the at least one radio frequency coil are provided for generating a time-varying spatial B1 field distribution in the subject. The time-varying spatial Bi field distribution time-integrates to define a spatial tip angle distribution in the subject having reduced spatial non-uniformity.
One advantage resides in providing flexible and effective compensation for B] field non-uniformity.
Another advantage resides in providing compensation for different types of patterns of Bs non-uniformity without using different compensation coils or other loading-specific hardware.
Another advantage resides in acquisition of more accurate magnetic resonance data with reduced effects of Bi non-uniformity.
Another advantage resides in improved reconstructed image quality. Another advantage resides in improved magnetic resonance spectra. Still further advantages of the present invention will be appreciated to those of ordinary skill in the art upon reading and understand the following detailed description.
The invention may take form in various components and arrangements of components, and in various steps and arrangements of steps. The drawings are only for purposes of illustrating the preferred embodiments and are not to be construed as limiting the invention.
FIGURE 1 diagrammatically shows a magnetic resonance scanner including a quadrature body coil, two independent radio frequency amplifiers separately driving the I and Q input ports of the quadrature body coil, and a two channel scanner controller with temporal sequencer for exciting a time-varying spatial B| field distribution.
FIGURE 2 diagrammatically shows the magnetic resonance excitation system of the magnetic resonance scanner of FIGURE 1 in greater detail.
FIGURE 3 show spatial Bi field distributions for modeling of an elliptical cardiac phantom placed in a quadrature body coil in a 3 Tesla magnetic field, for four different excitation conditions.
FIGURES 4 and 5 show spatial tip angle distributions produced by two different time-invariant Bi field distributions.
FIGURE 6 shows a spatial tip angle distribution for a time-integrated combination of the time-invariant Bi field distributions of FIGURES 4 and 5.
FIGURE 7 diagrammatically shows another magnetic resonance scanner employing a plurality of local coils in place of the quadrature body coil of FIGURE 1.
FIGURE 8 diagrammatically shows the magnetic resonance excitation system of the magnetic resonance scanner of FIGURE 7 in greater detail.
With reference to FIGURE 1, a magnetic resonance scanner 10 includes a scanner housing 12 in which a patient 16 or other subject is at least partially disposed. A protective insulating bore liner 18 of the scanner housing 12 optionally lines a generally cylindrical bore or opening of the scanner housing 12 inside of which the subject 16 is disposed. A main magnet 20 disposed in the scanner housing 12 is controlled by a main magnet controller 22 to generate a static (Bo) magnetic field in at least a scanning region including at least a portion of the subject 16. Typically, the main magnet 20 is a persistent superconducting magnet surrounded by cryoshrouding 24. In some embodiments, the main magnet 20 generates a main magnetic field of at least about 0.2 Tesla, such as 0.23 Tesla, 1.5 Tesla, 3 Tesla, 7 Tesla, or so forth. Magnetic field gradient coils 28 are arranged in or on the housing 12 to superimpose selected magnetic field gradients on the main magnetic field in at least the scanning region. Typically, the magnetic field gradient coils include coils for producing three orthogonal magnetic field gradients, such as x-gradient, y-gradient, and z-gradient.
A generally cylindrical quadrature body coil 30 is mounted substantially coaxially with the bore of the magnetic resonance scanner 10. In some embodiments, the quadrature body coil 30 is a permanent fixture mounted inside the scanner housing 12. In some embodiments, the quadrature body coil 30 is mounted on a dielectric former or other holder that can be slidably inserted into and removed from the bore of the magnetic resonance scanner 10, or slidably inserted into and removed from an annular receptacle of the scanner housing 12. In other embodiments, the quadrature coil 30 can be a local quadrature coil, such as a head quadrature coil or a knee quadrature coil. In some embodiments the quadrature body coil 30 is a quadrature birdcage coil including a plurality of rungs arranged generally parallel with the axis of the bore and operatively interconnected by two or more endrings, endcaps, or other terminating structures disposed at or near the opposite ends of the rungs. In some embodiments the quadrature body coil 30 is a quadrature transverse-electromagnetic (TEM) coil including a plurality of rods arranged generally parallel with the axis of the bore and operatively interconnected by a generally annular radio frequency shield or screen substantially surrounding the rods. The quadrature body coil 30 optionally includes capacitances, inductances, resistances, chokes, transistors, relays, or other components for providing radio frequency tuning, decoupling, current blocking or trapping, or other functionality.
In some embodiments, the quadrature body coil 30 performs both transmit and receive functions. That is, the quadrature body coil 30 is externally energized to excite magnetic resonance in the subject 16, and is also used to receive magnetic resonance signals generated by the excitation. In some embodiments, the quadrature body coil 30 performs the transmit function, and a separate receive coil 34 receives magnetic resonance signals generated by the excitation. The optional separate receive coil 34 can be a surface coil as illustrated, or a surface coils array, or an arm coil, leg coil, or other local coil. In some embodiments, the scanner 10 is configurable so that in some imaging applications the quadrature body coil 30 performs both transmit and receive functions while in other imaging applications the quadrature body coil 30 performs the transmit function and a separate receive coil performs the receive function. The optional separate receive coil 34 typically includes detuning circuitry that detunes the receive coil during the transmit phase to avoid overloading the receive coil.
With continuing reference to FIGURE 1 and with further reference to
FIGURE 2 which shows a magnetic resonance excitation system 36 of the magnetic resonance scanner of FIGURE 1 in greater detail, an I-channel radio frequency amplifier
38 generates an I-channel radio frequency drive signal having an amplitude Ai and a phase φι at the magnetic resonance frequency, while a Q-channel radio frequency amplifier 40 generates a Q-channel radio frequency drive signal having an amplitude AQ and a phase ΦQ at the same magnetic resonance frequency. The I-channel and Q-channel radio frequency drive signals are independent in that they may have different amplitudes Ai, AQ (within the limits imposed by the dynamic ranges of the amplifiers 38, 40) and different relative phases φi, ΦQ. The I-channel drive signal output by the I-channcl radio frequency amplifier
38 is fed into an I-channcl input port 42 of the quadrature body coil 30. The Q-channel drive signal output by the Q-channel radio frequency amplifier 40 is fed into a Q-channel input port 44 of the quadrature body coil 30.
If the I-channel and Q-channel radio frequency drive signals are of equal amplitude (AI=AQ) with a 90° phase difference between the I- and Q-channel radio frequency drive signals (ΦQI=90°), then the quadrature body coil 30 is operated in the usual quadrature mode that produces a B] field vector that rotates at the magnetic resonance frequency. However, if two separate RF waveform generators and two independent amplifiers 38, 40 are provided, there is in general no restriction on the I- and Q-channel radio frequency drive signal amplitudes Aj, AQ and the phase difference ΦQI therebetween.
With reference to FIGURE 1, optionally a magnetic field gradients controller 54 operates the magnetic field gradient coils 28 to spatially localize the magnetic resonance excitation to a slab or other localized region. Optionally, the magnetic field gradient controller 54 operates the magnetic field gradient coils 28 to apply one or more spatial encoding magnetic field gradient pulses.
In the embodiment of FIGURE 1, a radio frequency receiver 56 is operatively connected with the illustrated local coil 34 to read magnetic resonance signals during a readout phase of the magnetic resonance sequence. Alternatively, in some embodiments the radio frequency receiver 56 is operatively coupled with the I and Q channel input ports 42, 44 of the quadrature body coil 30 during the readout phase, with suitably radio frequency circuitry being provided to switch between operative connection of the quadrature body coil 30 with the radio frequency amplifiers 38, 40 during the transmit phase and operative connection with the radio frequency receiver 56 during the readout phase. Optionally, the magnetic field gradient controller 54 operates the magnetic field gradient coils 28 during the readout phase to provide additional spatial encoding (i.e., readout encoding) of the magnetic resonance signals.
The magnetic resonance samples acquired during the readout are stored in a data buffer 58. A magnetic resonance data processor 60 performs processing of the acquired magnetic resonance data to extract useful information. In imaging applications, the data processor 60 suitably performs image reconstruction using a Fast Fourier transform or other image reconstruction algorithms comporting with the selected spatial encoding applied during generation of the magnetic resonance data. In spectroscopic applications, the processing performed by the data processor 60 may include, for example, performing spectral fast Fourier transform operations to recover chemical shift and J-coupling data. The resulting processed data (e.g., images, spectra, or so forth) are suitably stored in a data/images memory 62, displayed on a user interface 64, printed, communicated over the Internet or a local area network, stored on a non-volatile storage medium, or otherwise used. In the example configuration illustrated in FIGURE 1, the user interface 64 also interfaces a radiologist or other operator with the scanner controller 66 to control the magnetic resonance scanner 10. In other embodiments, a separate scanner control interface may be provided.
With reference to FIGURES 1 and 2, the magnetic resonance excitation system 36 is configured to allow time-averaging of a Bλ (r) field so as to compensate for Bi spatial non-uniformity. In this notation, r denotes spatial position, so that B1 (T) denotes the spatial B| field distribution. Applying a time-invariant B] (F) field for a time τ produces a spatial tip angle distribution θ (F) given by:
Figure imgf000010_0001
where γ is the gyromagnetic ratio and Bx (F) is the component of the Bx (r) vector that
contributes to magnetic resonance excitation. For the time-invariant B1(F) field the component B1 +(F) is independent of time, and Equation (1) simplifies to:
θ(F) = γ|<(r)| -τ (2), where τ is the duration of application of the constant |B| "] field.
The magnetic resonance scanner 10 includes the capability of generating a time-varying spatial Bx (F) field distribution that varies in spatial shape, by independently controlling the 1 and Q channel radio frequency amplifiers 38, 40. Denoting the time-varying spatial 2J1 (F) field distribution as Bx (F J) where t denotes time, Equation (1 ) becomes:
Figure imgf000010_0002
If only a single radio frequency amplifier was used in conjunction with a hybrid circuit to produce the 1 and Q components, then the time- varying spatial Bx (Fj) field distribution could only be varied in amplitude or phase - that is, the spatial shape of the spatial Bx (F, t) field distribution could not be varied. This is the case with a typical MR system. In contrast, in the scanner 10 the time-varying spatial Bx (Fj) field distribution can have varying shape.
FIGURE 3 shows spatial Bx (F, t) field distributions for modeling of an elliptical cardiac phantom (aspect ratio = 19cm/35cm = 0.54, length = 34cm, conductivity = 0.5 S/m, and relative permittivity = 78) placed in a quadrature body coil in a 3 Tesla static (B0) magnetic field. FIGURE 3 shows the spatial Bx (FJ) field distributions for four conditions: Ai=I, AQ=O (i.e., driving only the I channel using the I-channel amplifier 38); A1=O, AQ=I (i.e., driving only the Q channel using the Q-channel amplifier 40); ApI,
Figure imgf000011_0001
(i.e., driving the quadrature body coil 30 in quadrature mode using both amplifiers 38, 40); and ApI, AQ= I , φp90°, ΦQ=O° (i.e., driving the quadrature body coil 30 in anti-quadrature mode using both amplifiers 38, 40). In the |B| H|-field maps of FIGURE 3 (as well as those of FIGURES 4-6), regions of about average [B]H |-field intensity are shown with whiter grayscale values; whereas, regions of low or high JBi+ - field intensity are shown with darker grayscale values. That is, relatively uniform regions arc whiter, while regions substantially contributing to non-uniformity are darker. Substantial spatial non-uniformities are seen for each of the coil operational modes, principally due to dielectric and eddy current effects in the cardiac phantom.
By suitably combining different spatial Zf1 (F, t) field distributions in time, a time-varying spatial Bi field distribution can be produced in a subject that time-integrates to define a spatial tip angle distribution in the subject having reduced spatial non-uniformity. The combination can be continuous, e.g. by applying Equation (3), or can involve combining two or more time-invariant spatial Bi field distributions each held constant over selected time interval τ. For example, the amplifiers 38, 40 can be controlled by the controller 66 to produce a first time-invariant spatial Bi field distribution Bi (r
( D over a time τ^ and a second time-invariant spatial Bs field distribution B^ (r) over a
(2) time τ2, the first and second time-invariant spatial Bi field distributions being different due to different RF excitation conditions. The combined tip angle Q (F) is given by a linear combination of Equation (2):
B[F) ^ y B{{r) t -X 1 +y B:{ή (4).
(I ) (2)
If a third time-invariant spatial Bi field distribution 5,+ (r) is applied
(3) over a time τ3, where the first, second, and third time-invariant spatial B| field distributions are different, then the resulting tip angle θ (F) is given by: θ (r) = γ |z?,+ (rj| -τ ι + γ *,f (r)|(2) -T2 + Y^(F) (5).
(3) More generally still, if N different time-invariant spatial Bi field distributions 5,+ (r)
OO are applied each for a selected time τn, where n=l ...N indexes the applied time-invariant spatial field distributions, then the resulting tip angle θ (F) is given by:
Figure imgf000012_0001
FIGURES 4-6 show an application of Equation (4). FIGURE 4 shows a spatial tip angle distribution B1 (V) produced by a time-invariant B^ (r) field
(i) distribution in which ApI , AQ=O.1 , φρθ°, ΦQ=40° applied for a time interval τj. FIGURE 5 shows a spatial tip angle distribution G2(F) produced by a time-invariant
5,+ (r) field distribution in which Ap0.4, Ao=0.9, φ,=120°, φQ=0° applied for a time
interval τ2. In the spatial tip angle distribution θt (F) of FIGURE 4, the central region represents a large tip angle of about 90-120°, while in the spatial tip angle distribution Θ2 (r) of FIGURE 5, the central region represents a small tip angle of about 0-40°.
FIGURE 6 shows a spatial tip angle distribution Θ(F) for the time-integrated combination of the time-invariant p/ (r) and
(i) /V (F) field
(2) distributions of FIGURES 4 and 5 combined in accordance with Equation (4) with Ti=T2. The field spatial tip angle distribution θ (F) of FIGURE 6 has a tip angle of 90°±9.25°, with a 67% decrease in standard deviation versus operation of the coil 30 in quadrature. While FIGURE 6 shows a combination of two different time-invariant Bi field distributions B^ (F) and B1 (/-) , it is anticipated that by selectively combining three
W (2) different time-invariant Bi field distributions in accordance with Equation (5), or four or more different time-invariant Bi field distributions in accordance with Equation (6), can provide still further reduced spatial nonuniformity in the spatial tip angle distribution θ (F) . In general, it can be expected that it will usually be possible to combine two selected different time-invariant Bi field distributions so as to produce a spatial tip angle distribution B (F) that is more spatially uniform than either constituent time- invariant spatial Bi field distribution. Similarly, it can be expected that a time- varying spatial Bi field distribution can be chosen to produce a spatial tip angle distribution that is more spatially uniform than the time- varying spatial B, field distribution.
With reference to FIGURES 1 and 2, the time-invariant spatial Bi field distribution used to create a more uniform spatial tip angle distribution can be either continuously varying (analyzed using Equation (3)) or discretely varying (analyzed using Equations (4)-(6)). In the continuously varying approach, the controller 66 controls the radio frequency amplifiers 38, 40 to generate output radio frequency signals with amplitudes A](t), AQ(t) and phases φ[(t), φQ(t) that are functions of time to produce a time-varying field distribution Bf (r,t) that time-integrates in accordance with Equation (3) to produce a spatial tip angle distribution θ (r) having reduced spatial non-uniformity. In the discretely varying approach, the controller 66 controls the radio frequency amplifiers 38, 40 to generate a temporal sequence of time-invariant output radio frequency signals each having amplitudes At(,,), AQ^J and phases φi(,,), ΦQ(,,) that produce time-invariant field distributions B] (r) that sum in accordance with Equation (6) to produce a spatial tip
angle distribution θ (r ) having reduced spatial non-uniformity. A temporal sequencer 70 determines suitable continuous functions As(t), AQ(t), φj(t), φo(t) or discrete values A](n), AQ(H), φ](n), ΦQ(,,) that provide the spatial tip angle distribution θ (r) having reduced spatial non-uniformity based on a determination of the coil loading imposed on the radio frequency coil 30 by a subject in the examination region. The determination of B| non-uniformity can be done in various ways. In some embodiments, a pre-scan is performed and an image of the subject reconstructed, and the B] non-uniformity estimated from the reconstructed image. In other embodiments, the B1 non-uniformity may be estimated based on measurements of the dimensions of the subject. For example, the shoulder width and chest diameter of a human subject may be measured to estimate the amount of Bi non-uniformity the human subject will impose upon the coil. In some embodiments, the temporal sequencer 70 includes a look-up table of continuous functions A|(t), AQ(I), φi(t), ΦQ(O or discrete values Aφ,), AQ(Π), φi(,,), ΦQ(Λ) that provide substantial uniformity for the spatial tip angle distribution Θ (F) . The look-up table values arc suitably pre-determined by finite element analysis simulations, or by experimental measurements on phantoms or human objects with different aspect ratios, or so forth. In other embodiments, the temporal sequencer 70 may include a finite element analysis electromagnetic simulator or other calculator for estimating suitable values of the continuous functions A[(t), AQ(I), φi(t), ΦQ(1) or discrete values A[(n), AQ^), φi(n), ΦQOU that provide substantial uniformity for the spatial tip angle distribution θ (F) . That is, in the discrete embodiment a composite Bi pulse or pulse packet is applied by the amplifiers 38, 40 which includes a series of two (Equation (4)), three (Equation (5)), or N (Equation (6)) sub-pulses which cumulatively produce the selected spatial tip angle distribution. Each sub-pulse has a selectable amplitude, phase, and/or duration to provide numerous degrees of freedom in tailoring the overall Bi pulse or pulse packet. In some embodiments, a sensor, sensor array or analyzer detects or measures the Bi field distribution to provide feedback 72 of the actual applied Bi field at the region of interest. In these embodiments, a series of pilot B| pulses are suitably applied and the detected or measured Bi field distribution is used by the temporal sequencer 70 to dynamically or iteratively adjust the Bj sub-pulses or Bj pulse shape to achieve the desired spatial tip angle distribution. For these embodiments, a dedicated sensor, sensor array or analyzer can be used, or the receive coil 34 can be used as the sensor, along with suitable processing performed by the data processor 60 or another processor, to produce the feedback 72 for dynamically or iteratively tailoring the Bi sub-pulses or Bi pulse shapes.
With reference to FIGURES 7 and 8, the technique of using a time-varying field distribution By {r,t) that time-integrates (for example, using a suitable one of
Equations (3)-(6)) to define a spatial tip angle distribution in the subject that is more spatially uniform than the time-varying spatial B] field distribution can be applied to other magnetic resonance excitation systems. A magnetic resonance scanner 10' includes a different magnetic resonance excitation system 36' in which the quadrature body coil 30 is replaced by an array of local coils 301, 302, 303. While three local surface coils 301, 302, 303 are shown, other types and/or numbers of local coils can be used. The I-channel and Q-channel radio frequency amplifiers 38, 40 are replaced by a set of three radio frequency amplifiers 40' that are independently controlled by the scanner controller 66. More generally, each local coil 301, 302, 303 has an input port that is coupled to its own independent amplifier - accordingly, the local coil 301 can be operated at amplitude Ai(t) and phase φi(t), the local coil 302 can be operated at amplitude A2(t) and phase φ2(t), and the local coil 303 can be operated at amplitude A3(t) and phase φ3(t). In the embodiment of FIGURE 7, the local coils 301, 302, 303 operate as transmit/receive CTVRx) coils that are selectively coupled with either the radio frequency amplifiers 40' or the radio frequency receiver 56 by a suitable switch 80. The time-varying Bi field distribution β,+ (r,f) is generated by the combination of local coils 301, 302, 303 based on the time-varying amplitudes Ai(t), A2(t), A3(t) and time-varying phases φs(t), φ2(t), φ3(t). As in the quadrature body coil embodiment, the time integration can be either continuous (where Aι(t), A2(t), A3(t), φi(t), φ2(t), φ3(t) are in general continuous functions of time) or discrete (where the amplitudes and phases are varied discretely, e.g. A|(tl), A2(H), A3(nj, φi(11), φ2ftl), φ3(n> where n=l ...N denotes the number of discrete time-invariant B] field distributions 5,+ that are combined in accordance with Equation (6).
Figure imgf000015_0001
The example magnetic resonance excitation systems 36, 36' are not exhaustive. As another example of a suitable magnetic resonance excitation system, a degenerate birdcage or TEM coil can be used, with individual rungs or rods driven by separate radio frequency amplifiers in accordance with the techniques disclosed herein.
It is to be appreciated that less than all of the coil parameters may be varied. For example, referencing back to the embodiment of FIGURES 1 and 2, in some instances it may be sufficient to keep As and φi constant (that is, the output of amplifier 38 is held constant) and to vary AQ and ΦQ continuously or discretely to effectuate the time-varying Bi field distribution B\ (r,t) . Indeed, it may be sufficient to vary only AQ or only ΦQ
continuously or discretely to effectuate the time-varying B; field distribution 5s + (r,f) .
The invention has been described with reference to the preferred embodiments. Modifications and alterations may occur to others upon reading and understanding the preceding detailed description. It is intended that the invention be constructed as including all such modifications and alterations insofar as they come within the scope of the appended claims or the equivalents thereof.

Claims

CLAIMSHaving thus described the preferred embodiments, the invention is now claimed to be:
1. A magnetic resonance scanner comprising: a main magnet (20, 22) for generating a static magnetic field at least in an examination region; a magnetic resonance excitation system (36, 36') including at least one radio frequency coil (30, 301, 302, 303) arranged to inject radio frequency energy into the examination region and at least two radio frequency amplifiers (38, 40, 40') coupled with different input ports of the at least one radio frequency coil; and a controller (66, 70) that controls the magnetic resonance excitation system to produce a time-varying spatial B[ field distribution in a subject (16) in the examination region that time-integrates to define a spatial tip angle distribution in the subject having reduced spatial non-uniformity.
2. The magnetic resonance scanner as set forth in claim 1, wherein the magnetic resonance excitation system (36) includes: a quadrature coil (30) having ϊ and Q input potts (42, 44); an I-channel radio frequency amplifier (38) coupled with the I input port; and a Q-channel radio frequency amplifier (40) coupled with the Q input port.
3. The magnetic resonance scanner as set forth in claim 2, wherein the quadrature coil (30) includes: more than two input ports; and two radio frequency amplifiers (38, 40), each amplifier coupled with one or more input ports.
4. The magnetic resonance scanner as set forth in claim 2, wherein the quadrature coil is one of a quadrature body coil (30) and a quadrature head quadrature coil.
5. The magnetic resonance scanner as set forth in claim 1, wherein the magnetic resonance excitation system (36) includes: a body coil (30) including two or more input ports (42, 44); and a radio frequency amplifier (38, 40) coupled with each input port.
6. The magnetic resonance scanner as set forth in claim 1, wherein the magnetic resonance excitation system (36') includes: a plurality of local coils (301, 302, 303) each having an input port; and a radio frequency amplifier (40') coupled with the input port of each local coil.
7. The magnetic resonance scanner as set forth in claim 1, wherein the controller (66, 70) controls the magnetic resonance excitation system (36, 36') to produce at least a first time-invariant spatial Bi field distribution over a time x\ and a second time-invariant spatial Bj field distribution over a time τ2, the first and second time-invariant spatial B] field distributions being different.
8. The magnetic resonance scanner as set forth in claim 7, wherein the controller (66, 70) controls the magnetic resonance excitation system (36, 36') to further produce a third time-invariant spatial B| field distribution over a time τ3, the first, second, and third time-invariant spatial Bi field distributions being different.
9. The magnetic resonance scanner as set forth in claim 1, wherein the controller (66, 70) controls the magnetic resonance excitation system (36, 36') to produce a continuously time-varying spatial B; field distribution over a time τ.
10. The magnetic resonance scanner as set forth in claim 1, wherein the controller (66, 70) controls the at least two radio frequency amplifiers (38, 40, 40') to output radio frequency signals including at least one time-varying radio frequency signal, the output radio frequency signals being coupled to the input ports of the at least one radio frequency coil (30, 301, 302, 303) to cause the radio frequency coil to produce the time- varying spatial B] field distribution.
11. The magnetic resonance scanner as set forth in claim 10, wherein the at least one time-varying radio frequency signal includes at least one of a time-varying amplitude and a time- varying phase.
12. The magnetic resonance scanner as set forth in claim 1, wherein the controller (66, 70) includes: a look-up table (70) specifying a plurality of different sets of radio frequency signals corresponding to different coil loadings of the at least one radio frequency coil (30, 301, 302, 303), each set of radio frequency signals being configured to be applied by the at least two radio frequency amplifiers (38, 40, 40') to produce a time-varying spatial Bj field distribution that time-integrates to define a spatial tip angle distribution having reduced spatial non-uniformity for the corresponding coil loading.
13. The magnetic resonance scanner as set forth in claim 1, wherein the controller (66, 70) controls each of the amplifiers (38, 40, 40f) to apply a composite pulse made up of a plurality of sub-pulses, each sub-pulse having a selectable amplitude, phase, and duration.
14. A magnetic resonance excitation method comprising: determining B§ non-uniformity imposed on at least one radio frequency coil
(30, 301, 302, 303) by a subject (16) coupled with the at least one radio frequency coil; and generating a time-varying spatial Bi field distribution in the subject using the at least one radio frequency coil, the time-varying spatial Bi field distribution time-integrating to define a spatial tip angle distribution in the subject that is more spatially uniform than the time-varying spatial B ; field distribution.
15. The magnetic resonance excitation method as set forth in claim 14, wherein the generating includes: generating a time-invariant Bi field distribution over a time interval; and generating a different time-invariant B j field distribution over an additional time interval.
16. The magnetic resonance excitation method as set forth in claim 15, wherein the generating further includes: generating another different time-invariant Bi field distribution over another additional time interval.
17. The magnetic resonance excitation method as set forth in claim 14, wherein the generating includes: generating a continuously time-varying Bi field distribution over a time interval.
18. The magnetic resonance excitation method as set forth in claim 14, wherein the generating includes: generating a composite pulse made up of a plurality of sub-pulses, each sub-pulse having a selectable amplitude, phase, and duration.
19. A magnetic resonance scanner with a controller (66, 70) programmed to operate the scanner according to the method of claim 14.
20. A magnetic resonance excitation apparatus comprising: means (10, 10') for determining a Bs non-uniformity imposed on at least one radio frequency coil by (30, 301, 302, 303) a subject (16) coupled with the at least one radio frequency coil; and means (36, 36', 66, 70) including the at least one radio frequency coil (30, 301, 302, 303) for generating a time-varying spatial Bi field distribution in the subject, the time-varying spatial Bi field distribution time-integrating to define a spatial tip angle distribution in the subject having reduced spatial non -uniformity.
21. The magnetic resonance excitation apparatus as set forth in claim 20, wherein the at least one radio frequency coil (30, 301, 302, 303) is a quadrature coil (30), and the generating means (36, 66, 70) further includes: two radio frequency amplifiers (38, 40) coupled with two quadrature ports (42, 44) of the quadrature coil, the operating of at least one of the two radio frequency amplifiers including outputting at least one of a time-varying radio frequency amplitude and a time-varying radio frequency phase.
22. The magnetic resonance excitation apparatus as set forth in claim 20, wherein the generating means (36, 36', 66, 70) includes: at least two radio frequency amplifiers (38, 40, 40') coupled with different input ports of the at least one radio frequency coil (30, 301, 302, 303), the operating of at least one of the radio frequency amplifiers including outputting at least one of a time-varying radio frequency amplitude and a time-varying radio frequency phase,
23. The magnetic resonance excitation apparatus as set forth in claim 20, wherein the at least one radio frequency coil (30, 301, 302, 303) includes a plurality of local coils (301, 302, 303).
24. The magnetic resonance excitation apparatus as set forth in claim 20, wherein the determining means (10, 10') includes: a sensor, sensor array or analyzer (34, 56, 60) for providing feedback (72) on the Bi field distribution.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100292564A1 (en) * 2009-05-18 2010-11-18 Cantillon Murphy Padraig J System and Method For Magnetic-Nanoparticle, Hyperthermia Cancer Therapy
CN102369451A (en) * 2009-03-31 2012-03-07 皇家飞利浦电子股份有限公司 Accelerated b1 mapping
EP2291672B1 (en) * 2008-06-20 2020-04-15 Koninklijke Philips N.V. Inductively powered electric component of an mri apparatus

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007124246A1 (en) * 2006-04-21 2007-11-01 Koninklijke Philips Electronics, N.V. Mr involving high speed coil mode switching between i-channel linear, q-channel linear, quadrature and anti-quadrature modes
JP5213849B2 (en) * 2006-04-21 2013-06-19 コーニンクレッカ フィリップス エレクトロニクス エヌ ヴィ Magnetic resonance by spin excitation of time sequence
US8072211B2 (en) * 2006-08-30 2011-12-06 Koninklijke Philips Electronics N.V. Multi-channel magnetic resonance imaging and spectroscopy
EP2223135A1 (en) * 2007-12-12 2010-09-01 Koninklijke Philips Electronics N.V. Transmit/receive coil for ultra-high field mri
DE102010033329B4 (en) * 2010-08-04 2012-10-31 Siemens Aktiengesellschaft Method and device for determining a magnetic resonance system drive sequence and method for operating a magnetic resonance system
US9714995B2 (en) * 2011-03-23 2017-07-25 Millikelvin Technologies Llc Techniques, systems and machine readable programs for magnetic resonance
US9423476B2 (en) * 2011-04-13 2016-08-23 New York University Apparatus, systems and methods for facilitating signal excitation and/or reception in a magnetic resonance system
JP5868025B2 (en) * 2011-05-23 2016-02-24 株式会社東芝 Magnetic resonance imaging system
US9791535B2 (en) 2012-05-16 2017-10-17 Wollin Ventures, Inc. Apparatus and method for mapping and measurement of spatially and temporally distributed induced small phase deviations in magnetic resonance utilizing deconvolution
JP6183025B2 (en) 2013-07-23 2017-08-23 ブラザー工業株式会社 Information processing program, information processing apparatus, and information processing apparatus control method
CN107850649B (en) * 2015-06-26 2020-11-03 皇家飞利浦有限公司 Magnetic resonance imaging system and method
DE102015222114A1 (en) 2015-11-10 2017-05-11 Siemens Healthcare Gmbh Method for driving a shim unit, control unit and magnetic resonance apparatus
CN109407021B (en) * 2018-11-23 2024-02-27 上海健康医学院 Magnetic resonance radio frequency shimming management system

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040150401A1 (en) * 2002-11-22 2004-08-05 Ludwig Eberler Method to correct the B1 field in MR measurements and MR apparatus for implementing the method
US20050194975A1 (en) * 2004-03-05 2005-09-08 Duensing G. R. Method and apparatus for serial array excitation for high field magnetic resonance imaging
US20050231203A1 (en) * 2004-03-18 2005-10-20 Thorsten Feiweier Method and magnetic resonance system for homogenizing the B1 field
US6975114B1 (en) * 2002-11-20 2005-12-13 Nova Medical, Inc. Methods for transmit excitation in magnetic resonance imaging using a transmit pulse with time varying spatial characteristics

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0179816B1 (en) * 1984-04-05 1992-11-11 Varian Associates, Inc. Spatially selective nuclear magnetic resonance pulse sequences
US7598739B2 (en) * 1999-05-21 2009-10-06 Regents Of The University Of Minnesota Radio frequency gradient, shim and parallel imaging coil
CA2334929A1 (en) * 2000-02-10 2001-08-10 Jarod Matwiy Quadrature rf field coil for use in magnetic resonance
US6946840B1 (en) * 2001-03-08 2005-09-20 General Electric Company Integrated and independently controlled transmit only and receive only coil arrays for magnetic resonance systems
DE10226511A1 (en) * 2002-06-14 2003-12-24 Philips Intellectual Property MR arrangement with high-frequency coil arrays
US6608480B1 (en) * 2002-09-30 2003-08-19 Ge Medical Systems Global Technology Company, Llc RF coil for homogeneous quadrature transmit and multiple channel receive
US7498809B2 (en) * 2002-12-27 2009-03-03 Hitachi Medical Corporation Magnetic resonance imaging device with multiple RF coils applying half-pulse waveforms for selective excitation of a local region
US7141973B2 (en) * 2003-08-13 2006-11-28 National Research Council Of Canada Magnetic resonance experiments by spatial encoding using the RF transmission coil
US6989673B2 (en) * 2003-11-26 2006-01-24 General Electric Company Method and apparatus to reduce RF power deposition during MR data acquisition
US7053618B2 (en) * 2003-11-26 2006-05-30 General Electric Company Method and apparatus to generate an RF excitation consistent with a desired excitation profile using a transmit coil array
CN101027569B (en) 2004-09-24 2011-03-16 皇家飞利浦电子股份有限公司 Magnetic resonance device and method
EP2899561B1 (en) * 2006-02-17 2021-04-28 Regents of the University of Minnesota MRI method for generating a map of the transmit RF field for each coil of a RF coil array
JP5213849B2 (en) * 2006-04-21 2013-06-19 コーニンクレッカ フィリップス エレクトロニクス エヌ ヴィ Magnetic resonance by spin excitation of time sequence
US7777488B2 (en) * 2007-07-12 2010-08-17 Vanderbilt University Methods for arbitrary shape selective excitation summed spectroscopy and applications of same
US8076939B2 (en) * 2008-04-10 2011-12-13 The General Hospital Corporation Method for fast magnetic resonance radiofrequency coil transmission profile mapping
DE102008021736B3 (en) * 2008-04-30 2009-12-10 Bruker Biospin Mri Gmbh Method for determining the spatial distribution of magnetic resonance signals when using local location-encoding magnetic fields
US8085046B2 (en) * 2008-08-28 2011-12-27 The General Hospital Corporation Coil array mode compression for parallel transmission magnetic resonance imaging

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6975114B1 (en) * 2002-11-20 2005-12-13 Nova Medical, Inc. Methods for transmit excitation in magnetic resonance imaging using a transmit pulse with time varying spatial characteristics
US20040150401A1 (en) * 2002-11-22 2004-08-05 Ludwig Eberler Method to correct the B1 field in MR measurements and MR apparatus for implementing the method
US20050194975A1 (en) * 2004-03-05 2005-09-08 Duensing G. R. Method and apparatus for serial array excitation for high field magnetic resonance imaging
US20050231203A1 (en) * 2004-03-18 2005-10-20 Thorsten Feiweier Method and magnetic resonance system for homogenizing the B1 field

Non-Patent Citations (8)

* Cited by examiner, † Cited by third party
Title
A.PESHKOVSKY ET AL.: "Open Volume TEM Quadrature Coil for High Field Imaging", PROC.INTL.SOC.MAG.RESON.MED., 2004, pages 1556, XP002440407 *
C.M.COLLINS ET AL.: "Strengths and Limitations of Pulsing Coils in an Array Sequentially to Avaoid RF Interference in High Field MRI", PROC.INTL.SOC.MAG.RESON.MED., 2005, pages 816, XP002440403 *
COLLINS C M ET AL: "Optimal Multiple-element Driving Configuration Depends on Head Geometry, Placement, and Volume of Interest", INTERNATIONAL SOCIETY FOR MAGNETIC RESONANCE IN MEDICINE. SCIENTIFIC MEETING AND EXHIBITION. PROCEEDINGS, INTERNATIONAL SOCIETY FOR MAGNETIC RESONANCE IN MEDICINE,, US, 2004, pages 1566, XP002420792, ISSN: 1524-6965 *
IBRAHIM T S ET AL: "Effect of RF coil excitation on field inhomogeneity at ultra high fields: A field optimized TEM resonator", MAGNETIC RESONANCE IMAGING, TARRYTOWN, NY, US, vol. 19, no. 10, December 2001 (2001-12-01), pages 1339 - 1347, XP002385099, ISSN: 0730-725X *
J.L.ULLOA ET AL.: "Exploring 3D RF shimming for slice selective imaging", PROC.INTL.SOC.MAG.RESON.MED., 2005, pages 21, XP002440404 *
M.H.LEVITT: "Symmetrical Composite Pulse Sequences for NMR Population Inversion. I. Compensation of Radiofrequency Field Inhomogeneity", JOURNAL OF MAGNETIC RESONANCE, vol. 48, 1982, pages 234 - 264, XP002440408 *
S.JUNGE ET AL.: "Integrated Coil-Setup for Multiple-Channel Transmit Applications at 200 MHz", PROC.INTL.SOC.MAG.RESON.MED., 2005, pages 918, XP002440406 *
U.KATSCHER ET AL.: "Static and Dynamic RF-shimming in the framework of Transmit SENSE", PROC.INTL.SOC.MAG.RESON.MED., 2005, pages 2256, XP002440405 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2291672B1 (en) * 2008-06-20 2020-04-15 Koninklijke Philips N.V. Inductively powered electric component of an mri apparatus
CN102369451A (en) * 2009-03-31 2012-03-07 皇家飞利浦电子股份有限公司 Accelerated b1 mapping
US20100292564A1 (en) * 2009-05-18 2010-11-18 Cantillon Murphy Padraig J System and Method For Magnetic-Nanoparticle, Hyperthermia Cancer Therapy

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