GB2056081A - NMR imaging - Google Patents
NMR imaging Download PDFInfo
- Publication number
- GB2056081A GB2056081A GB8023902A GB8023902A GB2056081A GB 2056081 A GB2056081 A GB 2056081A GB 8023902 A GB8023902 A GB 8023902A GB 8023902 A GB8023902 A GB 8023902A GB 2056081 A GB2056081 A GB 2056081A
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- GB
- United Kingdom
- Prior art keywords
- resonance
- field
- line
- gradient
- pulse
- Prior art date
- Legal status (The legal status 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 status listed.)
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Classifications
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01R—MEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
- G01R33/00—Arrangements or instruments for measuring magnetic variables
- G01R33/20—Arrangements or instruments for measuring magnetic variables involving magnetic resonance
- G01R33/28—Details of apparatus provided for in groups G01R33/44 - G01R33/64
- G01R33/38—Systems for generation, homogenisation or stabilisation of the main or gradient magnetic field
- G01R33/3808—Magnet assemblies for single-sided MR wherein the magnet assembly is located on one side of a subject only; Magnet assemblies for inside-out MR, e.g. for MR in a borehole or in a blood vessel, or magnet assemblies for fringe-field MR
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01R—MEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
- G01R33/00—Arrangements or instruments for measuring magnetic variables
- G01R33/20—Arrangements or instruments for measuring magnetic variables involving magnetic resonance
- G01R33/44—Arrangements or instruments for measuring magnetic variables involving magnetic resonance using nuclear magnetic resonance [NMR]
- G01R33/48—NMR imaging systems
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01R—MEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
- G01R33/00—Arrangements or instruments for measuring magnetic variables
- G01R33/20—Arrangements or instruments for measuring magnetic variables involving magnetic resonance
- G01R33/44—Arrangements or instruments for measuring magnetic variables involving magnetic resonance using nuclear magnetic resonance [NMR]
- G01R33/48—NMR imaging systems
- G01R33/483—NMR imaging systems with selection of signals or spectra from particular regions of the volume, e.g. in vivo spectroscopy
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01R—MEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
- G01R33/00—Arrangements or instruments for measuring magnetic variables
- G01R33/20—Arrangements or instruments for measuring magnetic variables involving magnetic resonance
- G01R33/44—Arrangements or instruments for measuring magnetic variables involving magnetic resonance using nuclear magnetic resonance [NMR]
- G01R33/48—NMR imaging systems
- G01R33/54—Signal processing systems, e.g. using pulse sequences ; Generation or control of pulse sequences; Operator console
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- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- High Energy & Nuclear Physics (AREA)
- Health & Medical Sciences (AREA)
- Signal Processing (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Vascular Medicine (AREA)
- Optics & Photonics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Magnetic Resonance Imaging Apparatus (AREA)
Abstract
The invention relates to small nuclear magnetic resonance pulse head 12 applicable to a body part in the manner of ultrasonic systems. An arrangement generates a field which varies in amplitude along a first direction, with distance from the head, the field being uniform at surfaces which intrude into the body. Resonance is excited in one such surface and a gradient applied orthogonally to the first direction restricts resonance to one line therein. The phase is then dispersed along the line and the signal sensed as a function of position therealong. <IMAGE>
Description
SPECIFICATION
Improvements in or relating to nuclear magnetic resonance systems
The present invention relates to systems for examining a body by nuclear magnetic resonance.
Nuclear magnetic resonance (NMR) is well known for examination of samples by spectroscopy. Recently it has been proposed to provide images of sectional slices or selected volumes. These procedures are useful in particular for medical examination of patients.
Such equipment is, however, relatively cumbersome comprising large coil systems which surround the patient.
It is an object of this invention to provide an arrangement incorporating relatively more compact equipment.
According to the invention there is provided a nuclear magnetic resonance apparatus including means for generating a steady magnetic field of strength which varies with distance therefrom, at least in a first direction being uniform at surfaces which can be caused to protrude into a body to be examined, means for exciting resonance for nuclei in the body, coinciding with a chosen surface, means for applying a field having a gradient in a second direction orthogonal to the first direction to restrict resonance to a line in the surface, means for dispersing the phase of the resonance along said line and means for sensing the dispersed resonance as a function of position in said line.
In order that the invention may be clearly understood and readily carried into effect it will now be described by way of example with reference to the accompanying drawings of which:
Figure 1 shows a yoke and coil for providing a
Z-field gradient,
Figure 2 shows the nature of the field so produced,
Figure 3 shows the position of the other coils and probes,
Figure 4 shows the examining pulse sequence used,
Figure 5 shows the examining head in perspective view,
Figure 6 shows the head in plan view,
Figure 7 is a block diagram of a circuit for the invention,
Figure 8 is a block diagram for the timing and control circuit of Figure 7,
Figure 9 is a block diagram of the field control cavity of Figure 7,
Figure 10 is a block diagram of the frequency control circuit, and
Figure 11 is a block diagram of the gradient control circuit of Figure 7.
Nuclei subject to a magnetic field have a resonant frequency related to the value of the field. Then by application of an R.F. magnetic field at the resonant frequency they can be excited and the excitation allowed to decay. The decay causes an induced signal at the resonant frequency in suitable coils.
Arrangements have been proposed, for
example as described in co-pending applications
Nos. 22291/78 and 7921 183, in which the
magnetic field is adjusted to have different values
in different parts of the body. A basic steady HzO-field in the Z-direction (usually axially of the
patient) is applied and also a further Hz-field having a gradient Gz f)Hz/z)Z. This provides a
unique total field value in a chosen cross-sectional
slice perpendicular to the Z-axis. Resonance is
excited preferentially in this slice and the
resonance signal therefrom can be detected.
Further field gradients in the plane of the slice are
applied to cause dispersion of the resonance frequencies to provide the basis for analysing the
signals to relate to different strips in the slice. If this is repeated for different strip patterns in the
slice the signals so obtained may be processed to
give an image of the slice.
However the coils used surround the patient entirely, being then both massive and expensive.
This invention uses a smaller geometry, at least
part of which can be placed in a relatively small
probe to be placed near to and to investigate a
limited region of the patient in a similar fashion to the procedure known for ultrasonic probes.
The basis of the probe is a magnet shown in
Figure 1 comprising a yoke 1 and a coil 2. This produces a field in the gap area which is non
uniform on all three of the axes shown, most significantly in the Z-direction.
Figure 2 shows the field in the gap, the field lines 3 being shown in solid line and the field contours 4 (lines of constant field) being shown in broken line. Figure 2 is merely indicative, the positions of the lines not being accurately computed.
The surfaces of constant field, shown in crosssection in Figure 2, are in fact curved surfaces, symmetrical in principle about the x and y axes.
They are very complex at the poles but it is not intended to make use of fields close to the poles.
Figure 3 shows a view of the probe from the direction A in Figure 1. Also shown are: coils 5 which provide a field having a gradient Gx in the x-direction; 6, which produce a gradient Gy in the y-direction; 7, which produce an R.F. field; and field sensing probes 8, which are of conventional type such as NMR probes.
Initially current is applied to coil 2 and is held so that the field is as nearly constant with time as is practicable, using the field probes 8 for a reference. This produces a gradient in field as shown in Figure 2. Following conventional NMR principles each surface of constant field has a respective resonance frequency for a particular substance. One of these is selected and there is applied an R.F. pulse at the resonant frequency for that slice. This is shown at 9 in Figure 4 which shows the complete pulse sequence.
It will be understood that the effect of the steady magnetic field is to cause nuclei, of the substance being investigated, to align their spins in the field direction. The R.F. field causes the spins to precess about the field direction with a precession angle which increases with increasing
R.F. field envelope integral. It is usual to identify the R.F. pulse with the precession angle it produces so that a 7r/2 pulse produces a 900 angle and a 7r pulse produces a 1800 angle.
In this example pulse 9 is a 7r/2 pulse. It should be noted that the longer the pulse, the thinner is the surface which is excited as more dephasing occurs due to the Z-gradient. Of course the height must be decreased to maintain the same precession angle.
After a time Ta short 1800 R.F. pulse 10 is applied to rephase the spins and produce a 'spinecho' as is now well known in NMR, The spin-echo itself will, following known principles, occur after a further delay of T equal to that between the 7r/2 and 7r pulses. The Z-gradient may be maintained during pulse 10 although that is not essential.
Thereafter the current in coil 2 is stopped so that the Z-gradient is removed, leaving the nuclei in the chosen shell resonating. After the 7r pulse 1 0 but before the spin-echo occurs there is applied an xgradient pulse 1 2 on coils 6. This disperses the phases of the nuclei except along the Gy = O line at which the resonance is maintained at the same frequency and phase. Thus the spin-echo, when it occurs, will be detected only on the line at which Guy=0.
After time T from the ir pulse 10, the spin-echo is detected by signal induced in this example in the R.F. coils 7, which are tuned to the appropriate frequency, although other specially designed coils could be used. As the spin-echo occurs, however, there is applied an x-gradient pulse 1 3 which disperses the spins along the selected line during the FID. The FID is then Fourier transformed to give a signal which varies with position along the line.
It will be appreciated that the line evaluated will be curved and not straight and the position may not be known with the accuracy of the larger machines. It will, however, give a useful indication of the quantity being measured which, by application of the probe external to a region of interest, can give at least a spot diagnosis of a gross condition.
The lines can be evaluated at different orientations and can be processed to give an image in the manner of prior art apparatuses.
The quantity being evaluated may be proton density, for water content, or may be density of nuclei of, say, potassium, phosphorus, ferros sulphate, sodium, barium, etc. It may be relaxation time.
Figure 5 shows a perspective view of the examining head enclosed in an outer case.
Figure 6 is a plan view of the head showing the internal disposition of the coils and corresponding to the side elevation of Figure 3. A typical head giving a field of about 0.1 Tesla over a volume of 200 mm3 may weigh 400 kg and will typically be 1000 mm diameter by 700 m long, so that it should be counterpoised on a moving gantry, not shown, in the manner of large conventional x-ray equipment.
Figure 7 shows a block diagram of the complete system. A timing and control unit 14 includes in read only memory the start and stop times, together with precalculated amplitudes and frequencies for the pulses. It controls coil 2 via an amplifier 1 5 to give the steady field and Zgradient. A field control 1 6 receives, via amplifier 1 7, signals from probes 8 and merely compares these with the instructed field and alters the coil current appropriately.
The frequency on the R.F. coils 7 is set by a frequency control 18. This includes an R.F.
oscillator whose timing and frequency are set from control 14. It should be noted that control 14 may include an operator input so that the field may be swept for a search procedure.
Similarly the x and y gradients are set by field drive and control unit 19, in response to control 14.
The signals sensed in the R.F. coils are demodulated in a known type of demodulator 20.
They are then taken into a RAM store 21 at the appropriate time. From there they are Fourier transformed in circuits 22, and entered into a further store 23. Stores 21 and 23 may be the same unit.
The output may be displayed on a suitable display 24.
The individual circuit elements shown in
Figure 7 are conventional to those familiar with nuclear magnetic resonance imaging and circuits for the control of similar equipment. However for further clarification suitable circuits for implementation of elements 14, 16, 1 8 and 1 9 are shown in block diagrammatic form in Figures 8, 9, 10 and 11 respectively.
Figure 8 then shows in more detail the timing and control arrangement 14. The control block shown at 25 provides the basic control input for the apparatus. This may simply be an operator control panel at which the operator selects the next operation required or may be a microprocessor holding a predetermined control pattern but will generally be a combination of those two. The control 25 supplies instructions to a sequence controller 26. This holds in read only memory a predetermined bit pattern array representing instruction pulses for each of the output lines for each instruction and provides these pulses at timing pulses from timing circuits 27 in response to instructions from 25. Circuits 27 comprise a system clock and appropriate counters and gates. It will be understood that circuits of this form are well known for controlling any sequence of operations which is known in advance and can readily be adapted to a chosen examination procedure.
The field control 1 6 shown in Figure 9 gates the field probe output from amplifier 1 7 with timing signals from 14 and takes a count in counter 28 which is in fact the measured field. Held in a staticiser 29, the measured field is compared in a subtractor 30 with the precalculated field (demand setting) from a store such as a read only memory 31. The consequent error signal is digitised in unit 32 to be applied to coil 12 via power amplifier is thereby to bring the field to the required value.
Figure 10 illustrates the frequency coil of unit 18. The R.F. field pulses 9 and 10 of Figure 4 are held in a profile store 33 as a sequence of amplitudes of the R.F. envelope at different times, these being precalculated for an examining sequence. The system clock in unit 14 provides pulses to a programmed address counter 34 which causes unit 33 to output the required amplitude sequence. A digital to analogue converter 35 controlled from 14 applies these to a mixer 36 where they are mixed with the R.F. from frequency synthesiser 37 fed by a master oscillator 38. The mixed signal is fed to the R.F.
coil while the R.F. from 37 is supplied to the demodulator 20.
Gradient control 19, as shown in Figure 11, also uses profile stores 39 and 40 holding the Gx and Gy pulse profiles also as precalculated amplitudes at different times. The profiles are clocked out with instructions timed by sequences 26 in unit 14, and clock pulses via address counter 41. These simply provide the digital amplitudes which are then converted to analogue form and amplified for application to the x and y coils.
In the foregoing circuits all of the stores holding timing sequences and profiles may be read only memory. However it will be appreciated that use of reprogrammable memories will allow the pulse sequence to be altered to modify the examination procedure to need.
Other embodiments of the invention will be apparent to those experienced with nuclear magnetic resonance.
Claims (14)
1. A nuclear magnetic resonance apparatus including means for generating a steady magnetic field of strength which varies with distance therefrom, at least in a first direction being
uniform at surfaces which can be caused to protrude into a body to be examined, means for
exciting resonance for nuclei in the body,
coinciding with a chosen surface, means for
applying a field having a gradient in a second
direction orthogonal to the first direction to restrict
resonance to a line in the surface, means for
dispersing the phase of the resonance along said
line and means for sensing the dispersed
resonance as a function of position in said line.
2. An apparatus according to claim 1 in which
the means for generating a steady magnetic field
is a yoke and a coil arranged to energise the yoke
to provide in the area of the gap thereof a field
being non-uniform at least in said first direction.
3. An apparatus according to either of the preceding claims in which the means for exciting includes coil system cooperating with drive circuits arranged to generate an R.F. field.
4. An apparatus according to claim 3 in which said R.F. coil system is used to sense said resonance signals.
5. An apparatus according to any of the preceding claims in which the means for dispersing include means generating a further field having a gradient substantially orthogonal to said first and second directions.
6. An apparatus according to claim 5 in which the means for generating said further field include field coils.
7. An apparatus according to any of the preceding claims including Fourier transform means arranged to cooperate with the means for sensing to provide signals representing amplitudes of resonance for different positions in said line.
8. An apparatus according to any of the preceding claims including a mobile probe which includes coils for generating said fields and sensing said resonance signals.
9. A nuclear magnetic resonance apparatus substantially as herein described with reference to the accompanying drawings.
10. A method of examining a body by nuclear magnetic resonance, the method including: generating a steady magnetic field which varies with distance in at least a first direction and which is uniform at surfaces which protrude into the body; exciting resonance of nuclei in the body which coincide with a chosen one of said surfaces; applying field having a gradient in a second direction, orthogonal to the first direction to restrict resonance to a line in the surface; and sensing the dispersed resonance signal as a function of positions in the line.
11. A method according to claim 10 in which said resonance is excited by application of an R.F.
magnetic field having a pulse envelope.
12. A method according to claim 11 in which the said pulse envelope is followed by a second pulse envelope of said R.F. field to cause a spinecho of said resonance.
13. A method according to claim 12 in which the first pulse envelope provides a w/2 pulse and the second pulse envelope provides a 7r pulse as herein defined.
14. A method according to claim 12 or claim 1 3 in which the said field having gradient in the second direction is applied prior to said spinecho and the said dispersion is obtained by applying, immediately following said spin-echo, a field having a gradient in a direction orthogonal to the first and second directions.
1 5. A method of examining a body by nuclear magnetic resonance, the method being substantially as herein described with reference to the accompanying drawings.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8023902A GB2056081B (en) | 1979-08-10 | 1980-07-22 | Nmr imaging |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7927965 | 1979-08-10 | ||
GB8023902A GB2056081B (en) | 1979-08-10 | 1980-07-22 | Nmr imaging |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2056081A true GB2056081A (en) | 1981-03-11 |
GB2056081B GB2056081B (en) | 1983-06-29 |
Family
ID=26272514
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8023902A Expired GB2056081B (en) | 1979-08-10 | 1980-07-22 | Nmr imaging |
Country Status (1)
Country | Link |
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GB (1) | GB2056081B (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2562250A1 (en) * | 1983-03-28 | 1985-10-04 | Us Energy | Nuclear magnetic resonance device comprising a semi-toroidal RF coil and intended for topical NMR and NMR imaging |
EP0171683A1 (en) * | 1984-08-09 | 1986-02-19 | Siemens Aktiengesellschaft | Apparatus for nuclear spin tomography |
EP0287661A1 (en) * | 1986-01-29 | 1988-10-26 | Yokogawa Medical Systems, Ltd | Scan controller for nmr imaging apparatus |
WO2007062255A2 (en) | 2005-11-27 | 2007-05-31 | Osteotronix, Limited | Assessment of structures such as bone using spatial-frequency analysis |
WO2015091749A1 (en) * | 2013-12-19 | 2015-06-25 | Sirona Dental Systems Gmbh | Unilateral magnetic resonance scanning device for medical diagnostics |
-
1980
- 1980-07-22 GB GB8023902A patent/GB2056081B/en not_active Expired
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2562250A1 (en) * | 1983-03-28 | 1985-10-04 | Us Energy | Nuclear magnetic resonance device comprising a semi-toroidal RF coil and intended for topical NMR and NMR imaging |
EP0171683A1 (en) * | 1984-08-09 | 1986-02-19 | Siemens Aktiengesellschaft | Apparatus for nuclear spin tomography |
US4932411A (en) * | 1984-08-09 | 1990-06-12 | Siemens Aktiengesellschaft | Intervivo coil for a nuclear magnetic resonance tomographic apparatus |
EP0287661A1 (en) * | 1986-01-29 | 1988-10-26 | Yokogawa Medical Systems, Ltd | Scan controller for nmr imaging apparatus |
EP0287661A4 (en) * | 1986-01-29 | 1990-11-28 | Yokogawa Medical Systems, Ltd | Scan controller for nmr imaging apparatus |
WO2007062255A2 (en) | 2005-11-27 | 2007-05-31 | Osteotronix, Limited | Assessment of structures such as bone using spatial-frequency analysis |
WO2007062255A3 (en) * | 2005-11-27 | 2007-10-04 | Osteotronix Ltd | Assessment of structures such as bone using spatial-frequency analysis |
US7932720B2 (en) | 2005-11-27 | 2011-04-26 | Acuitas Medical Limited | Magnetic field gradient structure characteristic assessment using one dimensional (1D) spatial-frequency distribution analysis |
CN101336380B (en) * | 2005-11-27 | 2013-01-30 | 精锐医药有限公司 | Assessment of structures such as bone using spatial-frequency analysis |
WO2015091749A1 (en) * | 2013-12-19 | 2015-06-25 | Sirona Dental Systems Gmbh | Unilateral magnetic resonance scanning device for medical diagnostics |
Also Published As
Publication number | Publication date |
---|---|
GB2056081B (en) | 1983-06-29 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
732 | Registration of transactions, instruments or events in the register (sect. 32/1977) | ||
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19920722 |