The Basics of MRI

Chapter 13

Advanced Imaging Techniques


Each year seems to bring a new application of MRI or a new pulse sequence which opens up new imaging opportunities with MRI. This section addresses some of these techniques. Each of the entries is not covered in depth due to space limitations. The reader is directed to the cited literature references for more detailed information.

Flow Imaging (MRI Angiography)

Angiography is the imaging of flowing blood in the arteries and veins of the body. In the past, angiography was only performed by introducing a x-ray opaque dye into the human body and making an X-ray image of the dye. This procedure produced a picture of the blood vessels in the body. It however did not produce an image which distinguished between static and flowing blood. It was therefore a less than adequate technique for imaging circulatory problems. Magnetic resonance angiography (MRA) on the other hand produces images of flowing blood. The intensity in these images is proportional to the velocity of the flow. There are three general types of MRA, time-of-flight , phase contrast angiography, and contrast enhanced angiography. They are described next.

Time-of-Flight Angiography

Time-of-flight angiography can be performed in several ways. One method uses a spin-echo sequence where the slice selective 90o and 180o pulses have different frequencies. The 90o pulse excites spins in one plane. The 180o pulse excites spins in another plane. In the absence of flow, no signal is seen because no spins experience both the 90o and 180o pulses. In the presence of flow and the correct TE time, blood from the 90o plane flows into the 180o plane and produces an echo.

Recall the following flow artifact description from Chapter 11. When the blood experiencing the 90o pulse does not experience the 180o pulse, no echo is observed. If the slice location of the 180o pulse is now changed to match the location of the blood which experienced the 90o pulse only that blood will contribute to the echo signal.

Phase Contrast Angiography

Phase contrast angiography is a little more complicated. The first new concept which you need to understand is that of a bipolar magnetic field gradient (GBP) pulse. A bipolar gradient pulse is one in which the gradient is turned on in one direction for a period of time then turned on in the opposite direction for an equivalent amount of time. A positive bipolar gradient pulse has the positive lobe first and a negative bipolar gradient pulse has the negative lobe first. The area under the first lobe of the gradient pulse must equal that of the second. A bipolar gradient pulse has no net effect on stationary spins. Spins which have a velocity component in the direction of the gradient will be effected by the bipolar gradient pulse.

For example, a stationary spin exposed to the first lobe of the bipolar gradient pulse will acquire a phase in radians given by

A = 2 γ x GBP dt
B = -2 γ x GBP dt

from the second lobe. If GBP of the two lobes are equal and the positions are equal during the two pulses the phase acquired from the A lobe equals that from the B lobe.

If this bipolar gradient pulse is placed in any one of the imaging sequences, in addition to the other gradients, it will not effect the image since all we have done is imparted a phase shift to the moving spins. Since an image is a magnitude representation of the transverse magnetization there is no effect. However if two imaging sequences are performed in which the first has a positive bipolar gradient pulse and the second a negative bipolar gradient pulse, and the raw data from the two is subtracted, the signals from the stationary spins will cancel and the flowing blood add. Look at the animation to convince yourself of this. A positive bipolar gradient pulse will have this effect on stationary and flowing spins, compared to a reference spin experiencing no gradient. A negative bipolar gradient pulse will have this effect on the same stationary and flowing spins.

If the vectors (and hence signals) from the positive and negative bipolar gradient pulses are subtracted, the vectors from the stationary spins cancel and the moving spins have a net magnitude. The net effect is an image of the flowing spins. From this animation it is easy to see that for optimum signal, you would like the vectors from the fastest flowing blood to acquire 90o of phase from each bipolar gradient pulse. Spins with lesser flow rates will acquire lesser phase shifts. The direction of the bipolar gradient yields signal from only those spins with a component in that direction.

A pulse sequence for one phase encoding gradient step of a phase contrast angiography sequence looks like this. Signals from the two parts are subtracted and used to produce that phase encoding line of the raw data.

Here are two examples of MRA images. The first is coronal projection of the flow in the head. The second is an axial projection through the brain.

Contrast Enhanced Angiography

Contrast enhanced angiography is based on the difference in the T1 relaxation time of blood and the surrounding tissue when a paramagnetic contrast agent is injected into the blood. This agent reduces the T1 relaxation times of the fluid in the blood vessels relative to surrounding tissues. When the data is collected with a short TR value, the signal from the tissues surrounding the blood vessels is very small due to its long T1 and the short TR. Images are recorded of the region of interest with rapid volume imaging sequences. The high quality of images from contrast enhanced MR angiography has made MRI the modality of choice for angiography.

Diffusion Imaging

Diffusion imaging can be performed in a manner similar to flow imaging using the phase contrast angiography sequence. The major difference is that the gradients must be increased in amplitude and/or the separation between the gradient pulses must be increased so as to image the much slower motions of molecular diffusion in the body. The reader is encouraged to review the previous phase contrast angiography section before proceeding.

The diffusion imaging sequence is usually implemented with a spin-echo sequence. The animation window contains a timing diagram with two repetitions of the sequence. Compared to the spin-echo sequence introduced previously, the diffusion sequence has an additional set of gradient pulses referred to as GD. The GD pulse is applied along the x, y, or z direction to obtain images of diffusion in the x, y, or z directions respectively. These two GD pulses are identical in amplitude and width (δ), separated by a time Δ, and placed symmetrically about the 180 degree pulse. The function of the GD pulses is to dephase magnetization from spins which have diffused to a new location in the period Δ. These pulses have no effect on stationary spins. For example, a stationary spin exposed to the first GD pulse, applied along the Z axis, will acquire a phase in radians given by

φ = 2 π γ z Gz dt

The spin will acquire an equal but opposite phase from the second pulse since the pulses are on different sides of the 180 degree RF pulse. Thus, their effects cancel each other out.

Consider the following illustration of the effect of the gradient pulses on the phase of stationary and moving spins. The illustration presents the phase of a diffusing spin relative to that of a reference spin and a stationary spin. The reference spin is one which experiences no gradient pulses. The stationary spin is not diffusing during the time illustrated by the sequence. The diffusing spin moves along Z during the sequence. The blue line in the timing diagram represents the time of the 180 degree pulse in the spin echo sequence. When you put the illustration into motion, the stationary spin comes back into phase with the reference one, indicating a positive contribution to the echo. The diffusing spin does not come back into phase with the reference spin so it diminishes the echo height.

The relationship between the signal (S) obtained in the presence of a GD in the i direction (Gi) and the diffusion coefficient in the same direction (Di) is given by the following equation where So is the signal at Gi=0.

S/So = exp[-(Gi γ δ)2 Di (Δ - δ/3)]

The diffusion coefficient is typically calculated from a plot of

ln(S/So) versus (Gi γ δ)2 (Δ - δ/3).

Again, diffusion in the x, y, or z direction is measured by applying GD respectively in the x, y, or z direction.

Diffusion imaging was initially used for assessing stroke. It has found additional application in studying the connectivity of the parts of the brain. This application is called diffusion tensor imaging (DTI) or diffusion tract imaging. In this application diffusion images are taken in x, y, and z. These images are used to create a diffusion tensor image. You can think of this image as a map of Dx, Dy, and Dz. Consider the following representation of 4 by 4 pixel portion of a diffusion tensor image. The two sided arrows represent the diffusion direction in the image plane. The underlying assumption of diffusion tract imaging is that the tissues in adjacent voxels are connected if there is high head-to-head diffusion in the same direction. This image indicates connectivity between pixels 4, 8, 12, and 16. There is also connectivity between the diagonal pixels from lower left to upper right. There is no connectivity between pixels 1, 2, 5, 11, 14, and 15 and any of the adjacent pixels. This pattern can be represented as vessels with the following inter pixel connectivity.

Here are two examples of diffusion tract images of the brain courtesy of A. Leemans.

Functional MRI

During brain activity there is a rapid momentary increase in the blood flow to the specific thought center in the brain. This results in an increase in the oxygen level of the blood in these regions. For example when you move your right index finger there is a rapid momentary increase in the circulation of the specific part of the brain controlling that movement of the finger. The increase in circulation means an increase in oxygen which is paramagnetic which affects the T2* of the local brain tissues. The difference in T2* relative to surrounding tissues causes a contrast between the tissues. This is referred to as the blood oxygen level dependent (BOLD) response.

Imaging the brain during activity will elicit the BOLD response. As you might imagine, it is a very weak (small signal difference) response requiring signal averaging. It is also a very rapid response and requires a fast imaging sequence. The echo-planar imaging sequence is fast enough to image many of these BOLD processes in the brain. Images are recorded of the brain with and without the stimulus and the difference image represents the bold response. The information in these images is overlaid on top of a generic brain map showing the regions which are active during a motor motion. The temporal resolution in fMRI is approximately 1 second.

Here is an example of functional imaging used to study the regions of the brain responsible for bilateral finger tapping. This image presents the regions of the brain experiencing the BOLD response and the change in the MRI signal at the intersection of the two blue lines in the previous image.

In Vivo NMR Spectroscopy

Nuclear magnetic resonance (NMR) spectroscopy in a clinical setting is the study of the specific resonance frequencies absorbed by a sample or tissue. These frequencies are related to the specific molecules present and can therefore be used to assess the disease state of a tissue. It is relatively easy to obtain an NMR spectrum of a bulk sample, but this is not very useful clinically. To improve the clinical utility of a spectral information, the spectrum must be from a small known location. Several techniques have been reported in the literature to obtain spectra from small regions in a sample. It is more difficult, and more clinically useful, to obtain an NMR spectrum from every voxel in an imaged object. Several methods have also been proposed for this form of spectroscopy. Examples of both types of techniques are summarized below. For additional techniques, the reader is directed to a good review by Matson and Weiner .

Mathematical Deconvolution Techniques

Deconvolution techniques are used to produce images of specific chemical components when some knowledge of composition of the sample and the NMR spectra of the components is known. In general, the techniques have limited utility. To understand them, consider the following one-dimensional imaging example. A sample is composed of two components, A and B, with concentrations CA and CB along x. The NMR spectrum of A has two absorption peak, and that of B has one. The image of CA+CB as a function of x is I(x). Notice that the image of the right spectral peak of A overlaps with that of B. Because the image from the left spectral peak is clearly defined, the overlap my be eliminated by subtraction. Images of A and B remain.

Surface Coil Techniques

Surface coil techniques are limited to regions near the surface of the imaged object. These techniques use the surface coil to produce the B1 magnetic field as well as detect the signal from tissues adjacent to the coil. The B1 magnetic field near a surface coil drops off as the distance from the coil increases. Therefore, the rotation angle of the spins decreases as the distance from the surface coil increases. If a high power RF pulse is applied to a surface coil, a large range of rotation angles will be obtained. Those regions experiencing an integer multiple of a 180 degree rotation will contribute no signal, while those experiencing odd multiples of a 90 degree rotation will see a maximum rotation and contribute most to the signal. The following is an example of the intensity variation seen in a sphere of water imaged with a coil placed off to one side.

Therefore, some localization of a spectrum can be obtained, but unfortunately the rotations of 270, 450, 630, ... will contribute a greater amount to the signal as the sensitivity of the surface coil is better the closer you get to the coil. One solution to this problem is to spoil the homogeneity of the Bo field close to the surface, thus eliminating signal from the 270, 450, 630, ... rotations. Bo field spoiling in this case can be accomplished by ferromagnetic materials or a grid of small electromagnets .

Sensitive Point Techniques

The variation in the Bo magnetic field over a region where a spectrum is to be recorded needs to be appreciably less than the line width of the spectral lines if spectral distortion is to be minimized. When the variation in the Bo is much greater than the line width, spectral lines are broadened. In extreme cases this broadening can prevent a line from being visible. The key to sensitive point techniques is to broaden the spectral lines from those regions where signal is not desired, and not distort lines from regions where they are wanted. The magnetic field distribution in the animation window will achieve this goal. In the presence of this one-dimensional gradient, only those spins experiencing the uniform magnetic field will produce a signal. This uniform Bo region can be moved around by changing currents through the coils producing the Bo function. To record the NMR spectrum from a specific region in a three-dimensional object, a Bo(y) and Bo(z) similar to the Bo(x) shown will be needed. This form of spectroscopic technique is also known as topical magnetic resonance (TMR) .

Slice Selective Techniques

Let's examine one technique using a multi-echo sequence. A slice selective RF pulse is applied in conjunction with a X magnetic field gradient. This excites spins in an YZ plane. A 180o slice selective RF pulse is applied in conjunction with a Y magnetic field gradient. This rotates spins located in an XZ plane. A second 180o slice selective RF pulse is applied in conjunction with a Z magnetic field gradient. The second 180o pulse excites spins in a XY plane. The second echo is recorded as the signal. This echo represents the signal from those spins in the intersection of the three planes. Fourier transforming the echo produces an NMR spectrum of the spins located at the intersection of the three planes. By prudent choice of the X, Y, and Z gradients the signal voxel can be positioned anywhere in the imaged object. This technique is referred to as point-resolved spectroscopy and given the acronym PRESS.

Several other approaches have appeared in the literature. The stimulated echo acquisition mode (STEAM) and selected volume excitation using stimulated echoes (VEST) techniques are similar to PRESS except a 90-90-90 pulse sequence is used instead of a 90-180-180 sequence. Image-selected in vivo spectroscopy (ISIS) uses three orthogonal slice-selective 180 degree pulses followed by a 90 degree pulse. The FID is collected after the 90 degree pulse. The three slice-selective 180 degree pulses are applied in specific combinations and the FIDs added or subtracted to produce a spectrum. The final technique in this category is depth-resolved surface spectroscopy (DRESS) . It consists of a single slice-selective 90 degree pulse followed by a rapidly applied gradient reversal pulse.

Spectroscopic Imaging Techniques

Spectroscopic imaging techniques are those that allow the scientist to record an NMR spectrum for each voxel in an image. The data from these techniques is generally three-dimensional (spatial-spatial-spectral) and therefore may be displayed as spectra for individual voxels or as images of a specific chemical shift. The easiest Spectroscopic Imaging Technique to understand is based on the 3-D or volume imaging technique, described earlier in Chapter 8, with a few modifications. The RF pulse is volume selective and the readout gradient (Gf) is turned off. The gradients labeled Gs and Gφ are cycled through their range of values to record spectra from all points in the spatial-spatial domain.

One additional spectroscopic imaging technique worth mentioning, especially because of its educational value, is spatial-spatial-spectral imaging based on the backprojection. Consider the following example using a one-dimensional sample to produce a spatial-spectral image. Assume the one-dimensional sample of length D has an NMR spectrum of width Ω with the following chemical shift components . Therefore, a spatial-spectral domain can be defined with the following data. The distribution of signal along the x axis can be imaged using a large one dimensional magnetic field gradient applied along x. This is equivalent to taking the projection of the data in the spatial-spectral domain onto the x-axis. A spectrum of the signals present in all three samples can be recorded by applying a homogeneous Bo field and recording the NMR signal. This is equivalent to taking the projection of the data onto the frequency axis.

The projection of the data in this spatial-spectral domain onto an axis located at an angle θ with respect to the frequency axis can be obtained by applying a magnetic field gradient, Gp, defined by the following equation.

tan θi = γ Gp D / Ω

The following pulse sequence is applied to obtain these projections. An RF pulse is applied to rotate magnetization by 90 degrees. The sequence is repeated i times and on each repetition the amplitude of the projection gradient, Gp, takes on a different value such that θi in the above equation takes on evenly spaced values between 0 and 2π. The projection data at the i different angles is backprojected to obtain an image of the NMR signal in the spatial-spectral plane, as was done in Chapter 6 for spatial-spatial imaging.

This technique has been implemented on a clinical imager to produce 1H spatial-spatial-spectral images. The images in the animation window are of an axial slice through the medial tibia. The θ = 90o image is a TR/TE=1000/35 ms spin-echo image. The remaining images represent those chemical shift components in the indicated ranges.

The most interesting NMR spectral components in the body are those of metabolites. The concentration of most metabolites is typically orders of magnitude less than that of the water or fat signal in tissues. Therefore, the 1H NMR signals from water and fat must be suppressed when performing 1H spectroscopy of metabolites.

Magnetization Transfer Contrast

Magnetization transfer contrast is a new method of increasing the contrast between tissues by physical rather than chemical means. For this technique to be effective, there must be at least two spin systems in the imaged anatomy which are capable of exchanging energy between themselves and one of the systems must have a much shorter T2 than the other system.

The pulse sequence looks very similar to the fat saturation imaging sequence described earlier in this chapter. A saturation pulse is applied with a frequency approximately 1 kHz from the center frequency. The saturation pulse is followed by a gradient-echo or spin-echo sequence.

The two spin systems could be protein and water. The protein has a very short T2 relative to the water T2. Because of the inverse relationship between T2 and the spectral linewidth, the NMR spectra of these two spin systems would have a very broad peak from the protein and a very narrow peak from the water. The signal from the protein will therefore not be visible in the image due to its broad linewidth which causes its signal to be spread out over the entire image. Applying the saturation pulse 1 kHz away from the center of these peaks could directly saturate the protein spin system and not the water. Any water molecules in contact with the protein might be capable of exchanging magnetization with the protein. Therefore saturating the protein will affect the signal of the water and the contrast between water in contact with the protein and not.

One way to picture magnetization transfer is to think of the water and protein spin systems as being energy reservoirs. In this picture there is a protein reservoir which is connected to a water reservoir, and another unconnected water reservoir. Energy can be placed in any one of the energy reservoirs and it will return to the lattice or surrounding molecules via spin-lattice relaxation.

Energy which is placed only in the protein reservoir by the frequency selective saturation pulse will influence the energy of the water spin system which is connected to it. If a pulse sequence is used to probe the magnetization of the two water spin systems while there is still energy in the protein connected water system, the protein connected water system will produce image intensity as if a short TR was used. The unconnected water system will produce image intensity as if a long TR was used. There will now be contrast between the two types of water, even if the T1 values for the two types of water are equivalent.

Variable Bandwidth Imaging

The amount of noise in an image is related to the sampling frequency of the FID or echo. The higher the sampling rate the more noise in the image. Similarly, lowering the sampling frequency allows less noise in the image. In the interest of improving the signal-to-noise ratio in an image, it is advantageous to use the smallest possible sampling rate. Since the sampling rate, fs, is related to the field of view (FOV), as seen in Chapter 7, the frequency encoding gradient, Gf, must be lowered proportionately to the sampling frequency in order to keep the FOV constant.

FOV = fs / γ Gf

Here is what the timing diagram would look like for a spin-echo sequence using a fast sampling frequency , and a slow sampling frequency .

There are three disadvantages associated with the use of a slower sampling frequency.

1. An increase in the chemical shift artifact. (See Chapter 11.)
2. A loss of contrast.
3. A restricted range of echo times, TE.

Here are two axial images through the human head at the level of the orbits. One image was recorded with a 16 kHz bandwidth and the other a 3 kHz bandwidth. . Notice that in the 3 kHz image there is a shift in the fat signals toward the anterior direction and a loss of contrast. The range of usable TE times in a spin-echo sequence is restricted with variable bandwidth imaging because, as the sampling rate decreases, the sampling window increases. .

In imaging applications where these three disadvantages do not matter, and an improved signal-to-noise ratio is needed, variable bandwidth imaging can be very beneficial.

T1, T2, and ρ Images

The spin-lattice relaxation time (T1), spin-spin relaxation time (T2), and the spin density (ρ) are properties of the of the spins in a tissues. The value of these quantities change from one normal tissue to the next, and from one diseased tissue to the next. They are therefore responsible for contrast between tissues in the various image types described in Chapter 7 and Chapter 8.

There are several methods of calculating T1, T2, and ρ values. These methods are applied to individual pixels to produce a calculated T1, T2, or ρ image. The smaller the voxel corresponding to a pixel, the more likely the T1, T2, and ρ values are to represent values for a single tissue. The larger the voxel, the more likely the calculated values are to represent that of a combination of tissue components.

The calculation of T1, T2, or ρ starts with the collection of a series of images. For example, if you wish to produce a T2 image, a spin-echo pulse sequence is used and a series of images are recorded with varying TE. The signal for a given pixel can be plotted for each TE value and the best fit line from the spin-echo equation drawn through the data to find T2.

A T1 image can be created from the same pulse sequence using a series of images with varying TR. The signal for a given pixel can be plotted for each TR value and the best fit line from the spin-echo equation drawn through the data to find T1. The spin density can be calculated once T1 and T2 are found using the spin echo signal equation and any spin echo signal.

The procedures just outlined will produce T1, T2, or ρ images, but are not the most efficient or accurate. The reader is directed to the scientific literature for more appropriate methods. ,

Tissue Classification

Tissue classification, or image segmentation as it is also called, is the identification of tissues in a magnetic resonance image. The classification is based on a property of the tissue in the image. For example, in this spin-echo image , where cerebral spinal fluid (CSF) and gray matter are bright compared to other tissues, the intensity of the pixel could be used to classify the tissue as CSF and gray matter or other tissues. The histogram and look up table for this image looks like this. Typically we would use a linear relationship between data value and pixel intensity. Furthermore the red, green, and blue content of each pixel would always be the same so as to get shades of grey for the pixels. We can segment the CSF and gray matter from other tissues in this example by modifying the lookup table such that the green and blue components of a pixel are turned off for data values greater than 865. This procedure will create red CSF and gray matter pixels. The image is therefore segmented into two classes of tissues: (1) gray matter and CSF, and (2) tissues other than gray matter and CSF.

The segmentation process is done with the aid of computer algorithms. These algorithms can segment with more advanced logic than the simple greater than a given data value example given above. Many different types of images, or spectral regions, can be used to segment the tissues. Some of the possible spectral regions include: T1, T2, and ρ weighted; pure T1, T2, and ρ; angiography; diffusion; chemical shift; and functional images. Some of these images are more difficult to work with. Images which show variations in sensitivity of an imaging coil can not be used because segmentation algorithms can not distinguish between an intensity variation caused by the imaging coil sensitivity and the tissue. Calculated T1, T2, and ρ images are easier to work with because they do not show the variation in intensity caused by variations in imaging coil sensitivity.

In the above example it was not possible to segment gray matter from CSF because the two tissues have similar intensities in the spin-echo image. The more independent spectral regions we work with the easier it is to segment tissues. For example, segmentation of the tissues in the brain can be accomplished with calculated T1 , T2 , and ρ images of the human brain. These images are used to create a three-dimensional histogram. Similar tissue types display clusters in the histogram. We can assign pixels in a given range of T1, T2, and ρ values a particular color. The resultant image displays the segmented tissues.

One additional segmentation example, based on morphology or texture in an image, is presented here. High resolution magnetic resonance images of the wrist are taken with a 0.7 mm slice thickness, an 8 cm FOV, and a 256x256 matrix. These images show the trabecular structure in the wrist bones. These images are used to train an algorithm to identify the different types of bone diseases by comparing their morphology. The resultant algorithm characterizes the trabecular structure and classify it based on known properties of diseased bones. The classified image depicts normal as red and those regions which have diminished trabecular or osteoporotic (green), cystic (blue), and sclerotic (light blue) properties.

Hyperpolarized Noble Gas Imaging

Hperpolarized noble gas imaging is the imaging of the NMR signal from a noble gas, such as 129Xe or 3He. Although it does not demonstrate the safety of inhaling Helium gas, many have done so to sound like Donald Duck. Xenon is used as an anesthetic, so much is known about the physiological effects of Xe, which in turn makes the imaging of hyperpolarized 129Xe easier. 129Xe is a spin 1/2 nucleus with a natural abundance of 26.44% and a gyromagnetic ratio of 11.8 MHz/T.

Hyperpolarized 3He and 129Xe are produced by a multistep process. First, Rb metal vapor in a magnetic field is optically excited with a 795 nm circularly polarized laser beam. This promotes an electron from the 5 2S1/2 spin -1/2 state ground state into the 5 2P1/2 spin +1/2 state. From here the atom undergoes external conversion to a the 5 2S1/2 spin +1/2 state. The Rb is said to be hyperpolarized as there are more Rb in the 5 2P1/2 spin +1/2 state then in the 5 2S1/2 spin -1/2 state. The polarized Rb vapor is next mixed with the nobel gas. The excited Rb electron looses energy by a spin exchange transfer to the He nucleus during He-Rb collisions. A similar process occurrs for Rb except nitrogen gas is needed and the collision between Rb and Xe results in a longer lived transition complex.

This process results in a net 129Xe nuclear magnetization of approximately 105 times that at equilibrium. The larger net magnetization means a larger signal is possible, and hence imaging of a gas is possible. The T1 of 129Xe is approximately three hours in vitro at 77 K and Bo=50 mT, and 1 to 50 s in vivo. Because we are dealing with a hyperpolarized gas with a long T1 value, all signal would be lost after the application of a 90o pulse. Therefore a gradient recalled echo with a 5o rotation angle is typically used to preserve signal throughout the acquisition period.

Here is an example of a spin-echo image of a rat brain. Superimposed on this image is a 32x32 pixel false color image of the 129Xe NMR signal in the brain from breathing hyperpolarized 129Xe for approximately 40 s. This study indicated that the 129Xe signal arose from within the brain and that there was a reduced Xe concentration in the cerebellum.

Magnetic Resonance Elastography (MRE)

Magnetic resonance elastography (MRE) is the imaging of shear waves using MRI. Contrast in MRE is related to the elastic modulus of the tissue. Magnetic resonance images are recorded while ultrasound waves are being sent into the imaged volume. This technique is expected to find application in locating pathology in soft tissue based on differences in the elastic modulus of the tissues. Hence, it has been referred to as magnetic resonance palpation.

Electron Spin Resonance (ESR)

Electron spin resonance (ESR), or electron paramagnetic resonance (EPR) as it is often called, is a magnetic resonance technique just like NMR. Unlike NMR, ESR is based on the spin of the electron rather than the spin of a nucleon. When placed in an external magnetic field, the spin of an unpaired electron can take on one of two orientations: aligned with, and opposed to the magnetic field. Just like in NMR, a photon with energy equal to the energy difference between the levels will cause a transition between the levels. ESR spectroscopy is a study of matter based of the energies absorbed in ESR. ESR imaging is the study of the spatial distribution of ESR signal bearing substances. Very few substances in nature have unpaired electrons. Therefore, very few substances can be studied with ESR. Nitroxide spin probes and some transition metals have an ESR signal. These substances have been studied directly by ESR, but are commonly used to probe biologic processes with ESR.

Due to the much smaller mass of an electron compared to a nucleon, the electronís gyromanetic ratio is about 658 times that of the protonís. Therefore, higher frequencies are used in ESR compared to NMR for the corresponding magnetic field strength. For a magnetic field of 1T electron spin resonance occurs approximately at 28.026 GHz, which is in the microwave region of the electromagnetic spectrum.

Go to the: [ next chapter | chapter top | previous chapter | cover ]

Copyright © 1996-2012 J.P. Hornak.
All Rights Reserved.