Short Transverse Relaxation Times Research Articles

Tendon evaluation with ultrashort echo time (UTE) MRI: a systematic review

Tendon disease ranks among the leading reasons patients consult their general practitioners, comprising approximately one-third of musculoskeletal appointments. Magnetic resonance imaging (MRI) is regarded as the gold standard for assessing tendons. Due to their short transverse relaxation time (T2), Tendons show up as a signal void in conventional MRI scans, which employ sequences with echo times (TEs) around several milliseconds. Ultrashort echo time (UTE) sequences utilize TEs that are 100–1,000 times shorter than those used in conventional sequences. This enables the direct visualization of tendons and assessment of their relaxation times, which is the basis for quantitative MRI. A systematic review was conducted on publications after 1990 in Google Scholar and PubMed databases. The search terms “ultrashort echo time,” “tendon,” and “UTE” were used to identify studies related to this investigation. This review discussed the current knowledge in quantitative UTE-MRI imaging of tendons. Quantitative UTE-T1, UTE-T2*, UTE-MT, and UTE-T1ρ techniques were described, and their reported applications in the literature were summarized in this review. We also discussed the advantages and challenges of these techniques and how these quantitative biomarkers may change in response to tendon pathology.

High-resolution myelin-water fraction and quantitative relaxation mapping using 3D ViSTa-MR fingerprinting.

This study aims to develop a high-resolution whole-brain multi-parametric quantitative MRI approach for simultaneous mapping of myelin-water fraction (MWF), T1, T2, and proton-density (PD), all within a clinically feasible scan time. We developed 3D visualization of short transverse relaxation time component (ViSTa)-MRF, which combined ViSTa technique with MR fingerprinting (MRF), to achieve high-fidelity whole-brain MWF and T1/T2/PD mapping on a clinical 3T scanner. To achieve fast acquisition and memory-efficient reconstruction, the ViSTa-MRF sequence leverages an optimized 3D tiny-golden-angle-shuffling spiral-projection acquisition and joint spatial-temporal subspace reconstruction with optimized preconditioning algorithm. With the proposed ViSTa-MRF approach, high-fidelity direct MWF mapping was achieved without a need for multicompartment fitting that could introduce bias and/or noise from additional assumptions or priors. The in vivo results demonstrate the effectiveness of the proposed acquisition and reconstruction framework to provide fast multi-parametric mapping with high SNR and good quality. The in vivo results of 1 mm- and 0.66 mm-isotropic resolution datasets indicate that the MWF values measured by the proposed method are consistent with standard ViSTa results that are 30× slower with lower SNR. Furthermore, we applied the proposed method to enable 5-min whole-brain 1 mm-iso assessment of MWF and T1/T2/PD mappings for infant brain development and for post-mortem brain samples. In this work, we have developed a 3D ViSTa-MRF technique that enables the acquisition of whole-brain MWF, quantitative T1, T2, and PD maps at 1 and 0.66 mm isotropic resolution in 5 and 15 min, respectively. This advancement allows for quantitative investigations of myelination changes in the brain.

Pushing the Detection Limit of Static Wideline NMR Spectroscopy Using Ultrafast Frequency-Swept Pulses.

We report a simple design strategy for wideband uniform-rate smooth truncation (WURST) pulses that enables ultrafast frequency sweeps to maximize the sensitivity of Carr-Purcell-Meiboom-Gill (CPMG) acquisition in static wideline nuclear magnetic resonance (NMR). Three compelling examples showcase the advantage of ultrafast frequency sweeps over currently employed WURST-CPMG protocols, demonstrating the potential of investigating materials that are typically inaccessible to static wideline NMR techniques, e.g., paramagnetic solids with short homogeneous transverse relaxation times.

Optimal-Control-Based Cβ Chemical Shift Encoding for Efficient Signal Assignment of Solid Proteins.

Fast magic-angle spinning (MAS) solid-state NMR spectroscopy is a powerful tool for gaining structural and dynamic information on solid proteins. To access such information site-specifically, the signal assignment process is unavoidable. In the assignment process, Cα and Cβ chemical shifts are of paramount importance in identifying the type of amino acid residues. Conventionally, however, recording the Cβ chemical shift of solid proteins with relatively short transverse relaxation time is often limited by the long delay required for the magnetization transfer to Cβ spins and its evolution, that is, by the sensitivity drop. In this article, we propose a new method that encodes the Cβ chemical shifts onto the intensities of the scalar-coupled Cα signals by combining an optimal control-based spin manipulation pulse and a spin-state filter. This reduces the total required transverse evolution to less than half of that for the previously proposed method, opening up the concept of the Cβ-encoding nearest-neighbor NMR, for the first time, to solid proteins. Also, the total measurement time was shorter than that required for the explicit Cβ shift evolution. We demonstrate the sequential signal assignment for microcrystalline protein GB1, and then discuss the prospects for more challenging proteins.

Ultra-high field magnetic resonance imaging of the quadriceps tendon enthesis in healthy subjects.

Although enthesitis is a hallmark of several rheumatologic conditions, current imaging methods are still unable to characterize entheses changes because of the corresponding short transverse relaxation times (T2). A growing number of MR studies have used Ultra-High Field (UHF) MRI in order to assess low-T2 tissues e.g., tendon but never in humans. The purpose of the present study was to assess in vivo the enthesis of the quadriceps tendon in healthy subjects using UHF MRI. Eleven healthy subjects volunteered in an osteoarthritis imaging study. The inclusion criteria were: no knee trauma, Lequesne index = 0, less than 3h of sport activities per week, and Kellgren and Lawrence grade = 0. 3D MR images were acquired at 7T using GRE sequences and a T2* mapping. Regions of interest i.e., trabecular bone, subchondral bone, enthesis, and tendon body were identified, and T2* values were quantified and compared. Quadriceps tendon enthesis was visible as a hyper-intense signal. The largest and the lowest T2* values were quantified in the subchondral bone region and the tendon body respectively. T2* value within subchondral bone was significantly higher than T2* value within the enthesis. T2* in subchondral bone region was significantly higher than the whole tendon body T2*. A T2* gradient was observed along the axis from the enthesis toward the tendon body. It illustrates different water biophysical properties. These results provide normative values which could be used in the field of inflammatory rheumatologic diseases and mechanical disorders affecting the tendon.

Myelin‐weighted MR Imaging in Patients with Alzheimer’s Disease

AbstractBackgroundDeveloping an imaging technique to map myelin changes in the brain within a short scan time is needed due to the inability of Alzheimer’s disease (AD) patients to remain motionless during MRI scanning.PurposeTo investigate myelin loss in both AD and mild cognitive impairment (MCI) patients with a new myelin water mapping technique within reasonable scan time and evaluate the clinical relevance of the apparent myelin water fraction (MWF) values by assessing the relationship between decreases in myelin water and the degree of memory decline or aging.MethodIn this prospective study from March 2019 to October 2021, the participants were allocated as follows: 29 individuals were assigned to the cognitively normal (CN) elderly group (mean ± SD, 73 ± 5 years, 16 females), 32 participants were assigned to the MCI group (74 ± 5 years, 21 females), and 31 patients were assigned to the AD group (74 ± 6 years, 26 females). A 3D visualization of the short transverse relaxation time component (ViSTa)‐gradient and spin‐echo (GraSE) sequence was developed to map apparent MWF. Then, the MWF values were compared between the three participant groups, and was evaluated the relationship with the degree of memory loss.ResultA total of 92 participants were evaluated. The AD group showed a reduced apparent MWF compared to the CN and MCI groups. Moreover, the MWF was decreased with age and positively correlated with Mini‐Mental State Examination scores. The largest AUC value (0.799) was in the corpus callosum and used to classify the CN and AD groups using the apparent MWF.ConclusionThe ViSTa‐GraSE sequence can be a useful tool to map the MWF in a reasonable scan time. Combining the MWF in the corpus callosum with the detection of atrophy in the hippocampus can be valuable for group classification.FundingThe research was supported by the National Research Foundation of Korea (NRF) grant funded by Ministry of Science and ICT (No. 2020R1A2C1004749, GHJ), Republic of Korea.

Design of a three-loop asymmetric coil producing a homogeneous radiofrequency B1 field gradient along the axis of a vertical sample tube

A coil system generating a vertical radio-frequency (rf) field gradient (B1 gradient) has been built for surrounding, in a horizontal magnet, a vertical sample (object) of axial symmetry. The system comprises three coaxial loops with an overall shape either spherical or ellipsoidal. The geometry has been theoretically and experimentally devised for producing a very uniform gradient (cancellation of B1 derivatives from second order up to sixth order) in the central region where a vertical receiver/transmitter coil is installed. The latter is of the saddle-shaped type and is geometrically and electrically decoupled from the gradient coil system. This receiver/transmitter coil not only ensures an optimal signal reception but, in addition, is able to deliver perfectly homogeneous rf hard pulses which are mandatory in most NMR experiments. In its present design, the system delivers a uniform gradient in a limited region but could be extended at will. Its main advantages over static field gradients (B0 gradients) appear clearly in the case of very short transverse relaxation times. This property has been emphasized in the case of experiments leading to the measurement of diffusion coefficients. Also, this system would be suitable for chemical shift imaging (CSI) experiments as confirmed by a preliminary test experiment.

Lysozyme impacts gel properties of egg white protein via electrostatic interactions, polarity differences, local pH regulation, or as a filler

The effects of lysozyme on egg white gel properties and their underlying causes were investigated under comparison between lysozyme removed with ion exchange resin and three levels of commercial lysozyme powder (1/2, 2/2, 3/2 the natural concentration in egg white) re-added in the lysozyme-removed system. Results showed that a lysozyme-removed gel obtained the best water holding capacity (61.61 %), lowest cooking loss (11.85 %), and enhanced textural properties (hardness, 638.04 g; resilience, 0.57; and gumminess), which was attributed to lysozyme promoting protein aggregation and weakening electrostatic repulsion by charge neutralization and competition for water, and this could be eliminated by removing lysozyme. Besides, the stronger intermolecular interactions (enhanced ionic bonds, hydrogen bonds and inhibited hydrophobic interactions), the shorter transverse relaxation time (T21 and T22), as well as more uniform microstructure formed in the lysozyme-removed gel, allowing the gels to bind more water molecules. With return of lysozyme, the gel properties were weakened to varying degrees, which was also ascribed to the filling of lysozyme in gel matrix narrowed interspace for binding and storage of water. In sum, adjustment on the content of lysozyme can regulate the gel properties of egg white, so as to obtain gels with regulable gel quality and processing characteristics.

Optimization of two-dimensional T1*–T2* relaxation correlation measurements in shale

Shale reservoirs, composed of fine-grained and organic-rich sedimentary rock, are common unconventional oil and gas reservoirs. Magnetic resonance (MR) relaxometry, a non-destructive and non-invasive method, is a key technique for shale evaluation. The T1*–T2* relaxation correlation, a rapid two-dimensional MR measurement, is a newly emerging and powerful tool to study the structure of materials with short transverse relaxation times. T1* and T2* are the effective longitudinal and transverse relaxation times. T1*–T2* measurement is a promising laboratory method to analyze fluid and organic matter components in shale, but it is very sensitive to the acquisition parameters. In this paper, the effects of acquisition parameters, including flip angle α, initial interval τ1, α pulse interval τ, and scan number, on T1*–T2* relaxation correlation of shale were analyzed by numerical simulations and core plug experiments. The optimized T1*–T2* measurement can be two orders of magnitude faster than a simple T1–T2* measurement. This work provides a theoretical and practical guide for undertaking T1*–T2* measurements, which should be helpful for further laboratory study of shale.

Myelin-Weighted Imaging Presents Reduced Apparent Myelin Water in Patients with Alzheimer's Disease.

The purpose of this study was to investigate myelin loss in both AD and mild cognitive impairment (MCI) patients with a new myelin water mapping technique within reasonable scan time and evaluate the clinical relevance of the apparent myelin water fraction (MWF) values by assessing the relationship between decreases in myelin water and the degree of memory decline or aging. Twenty-nine individuals were assigned to the cognitively normal (CN) elderly group, 32 participants were assigned to the MCI group, and 31 patients were assigned to the AD group. A 3D visualization of the short transverse relaxation time component (ViSTa)-gradient and spin-echo (GraSE) sequence was developed to map apparent MWF. Then, the MWF values were compared between the three participant groups and was evaluated the relationship with the degree of memory loss. The AD group showed a reduced apparent MWF compared to the CN and MCI groups. The largest AUC (area under the curve) value was in the corpus callosum and used to classify the CN and AD groups using the apparent MWF. The ViSTa-GraSE sequence can be a useful tool to map the MWF in a reasonable scan time. Combining the MWF in the corpus callosum with the detection of atrophy in the hippocampus can be valuable for group classification.

Correlation between the elastic modulus of anterior cruciate ligament (ACL) and quantitative ultrashort echo time (UTE) magnetic resonance imaging.

Conventional magnetic resonance imaging (MRI) often acquires no signal in anterior cruciate ligament (ACL) due to the short apparent transverse relaxation time of ACL. Ultrashort echo time (UTE) MRI is capable of imaging ACL with high signal which enables quantitative ACL assessment. This study aimed to investigate the correlations of the mechanical and microstructural properties of human ACL specimens with quantitative three-dimensional UTE Cones (3D-UTE-Cones) MRI measures. ACL specimens were harvested from cadaveric knee joints of 13 (50.9 ± 21.1 years old, 11 males and 2 female) donors. Specimens were scanned using a series of quantitative 3D-UTE-Cones T2 * (UTE-T2 *), T1 (UTE-T1 ), Adiabatic T1ρ (UTE-Adiab-T1ρ ), and magnetization transfer (UTE-MT) sequences in a wrist coil on a clinical 3T scanner. ACL elastic modulus was measured using a uniaxial tensile mechanical test. Histomorphometry analysis was performed to measure the average fascicle specific surface, fascicle size, and number of cells per unit area. Spearman's rank correlations of UTE-MRI biomarkers with mechanical and histomorphometry measures were investigated. The elastic modulus of ACL showed significant moderate correlations with UTE-Adiab-T1ρ (R = -0.59, p = 0.01), macromolecular fraction from MT modeling (R = 0.54, p = 0.01), magnetization transfer ratio (R = 0.53, p = 0.01), UTE-T2* (R = -0.53, p = 0.01), and average fascicle specific surface (R = 0.54, p = 0.01). UTE-MRI showed nonsignificant correlations with histomorphometry measures. UTE-MRI biomarkers may be useful noninvasive tools for the ACL mechanical assessment.

Magnetic Resonance Imaging Versus Computed Tomography for Three-Dimensional Bone Imaging of Musculoskeletal Pathologies: A Review.

Magnetic resonance imaging (MRI) is increasingly utilized as a radiation‐free alternative to computed tomography (CT) for the diagnosis and treatment planning of musculoskeletal pathologies. MR imaging of hard tissues such as cortical bone remains challenging due to their low proton density and short transverse relaxation times, rendering bone tissues as nonspecific low signal structures on MR images obtained from most sequences. Developments in MR image acquisition and post‐processing have opened the path for enhanced MR‐based bone visualization aiming to provide a CT‐like contrast and, as such, ease clinical interpretation. The purpose of this review is to provide an overview of studies comparing MR and CT imaging for diagnostic and treatment planning purposes in orthopedic care, with a special focus on selective bone visualization, bone segmentation, and three‐dimensional (3D) modeling. This review discusses conventional gradient‐echo derived techniques as well as dedicated short echo time acquisition techniques and post‐processing techniques, including the generation of synthetic CT, in the context of 3D and specific bone visualization. Based on the reviewed literature, it may be concluded that the recent developments in MRI‐based bone visualization are promising. MRI alone provides valuable information on both bone and soft tissues for a broad range of applications including diagnostics, 3D modeling, and treatment planning in multiple anatomical regions, including the skull, spine, shoulder, pelvis, and long bones.Level of Evidence3Technical EfficacyStage 3

Asymmetry of EPR signal response in nuclear magnetic resonance gyroscope

The spin relaxation time of alkali atoms in nuclear magnetic resonance gyroscope is usually on the order of 10<sup>–5</sup> s, which is much less than that in atomic magnetometers. The response of electron paramagnetic resonance signals of atoms with short relaxation time is asymmetric in different directions under oscillating magnetic fields, which makes the measurement results of atomic transverse relaxation time and Larmor frequency different. In this work this phenomenon is analyzed based on Bloch equation theory and the theoretical correction is given. The shorter the relaxation time, the greater the differences of the response intensity and resonance frequency of the electron paramagnetic resonance signal under different magnetic field directions will be. Using this property, the transmission delay time of the system can be measured accurately. In this paper proposed is a method of measuring transverse relaxation time based on the difference between signal phases in <i>X</i>-axis direction and <i>Y</i><italic/>-axis direction, which can accurately and quickly measure very short transverse relaxation time. The difference between the half-width fitting method and the phase measurement method is compared by measuring the transverse relaxation times of <sup>87</sup>Rb atoms under different magnetic field intensities. The half-width fitting method is greatly affected by the transmission delay time and has its measurement limit. The phase measurement method is greatly affected by the angle of the probe light, but the measurement range is wider and the anti-magnetic interference ability is stronger.

Assessing the differential sensitivities of wave-CAIPI ViSTa myelin water fraction and magnetization transfer saturation for efficiently quantifying tissue damage in MS

BackgroundWave-CAIPI Visualization of Short Transverse relaxation time component (ViSTa) is a recently developed, short-T1-sensitized MRI method for fast quantification of myelin water fraction (MWF) in the human brain. It represents a promising technique for the evaluation of subtle, early signals of demyelination in the cerebral white matter of multiple sclerosis (MS) patients. Currently however, few studies exist that robustly assess the utility of ViSTa MWF measures of myelin compared to more conventional MRI measures of myelin in the brain of MS patients. Moreover, there are no previous studies evaluating the sensitivity of ViSTa MWF for the non-invasive detection of subtle tissue damage in both normal-appearing white matter (NAWM) and white matter lesions of MS patients. As a result, a central purpose of this study was to systematically evaluate the relationship between myelin sensitivity of T1-based ViSTa MWF mapping and a more generally recognized metric, Magnetization Transfer Saturation (MTsat), in healthy control and MS brain white matter. MethodsViSTa MWF and MTsat values were evaluated in automatically-classified normal appearing white matter (NAWM), white matter (WM) lesion tissue, cortical gray matter, and deep gray matter of 29 MS patients and 10 healthy controls using 3T MRI. MWF and MT sat were also assessed in a tract-specific manner using the Johns Hopkins University WM atlas. MRI-derived measures of cerebral myelin content were uniquely compared by employing non-normal distribution-specific measures of median, interquartile range and skewness. Separate analyses of variance were applied to test tissue-specific differences in MTsat and ViSTa MWF distribution metrics. Non-parametric tests were utilized when appropriate. All tests were corrected for multiple comparisons using the False Discovery Rate method at the level, α=0.05. ResultsDifferences in whole NAWM MS tissue damage were detected with a higher effect size when using ViSTa MWF (q = 0.0008; ƞ2 = 0.34) compared to MTsat (q = 0.02; ƞ2= 0.24). We also observed that, as a possible measure of WM pathology, ViSTa-derived NAWM MWF voxel distributions of MS subjects were consistently skewed towards lower MWF values, while MTsat voxel distributions showed reduced skewness values. We further identified tract-specific reductions in mean ViSTa MWF of MS patients compared to controls that were not observed with MTsat. However, MTsat (q = 1.4 × 10−21; ƞ2 = 0.88) displayed higher effect sizes when differentiating NAWM and MS lesion tissue. Using regression analysis at the group level, we identified a linear relationship between MTsat and ViSTa MWF in NAWM (R2 = 0.46; p = 7.8 × 10−4) lesions (R2 = 0.30; p = 0.004), and with all tissue types combined (R2 = 0.71; p = 8.4 × 10−45). The linear relationship was also observed in most of the WM tracts we investigated. ViSTa MWF in NAWM of MS patients correlated with both disease duration (p = 0.02; R2 = 0.27) and WM lesion volume (p = 0.002; R2 = 0.34). ConclusionBecause ViSTa MWF and MTsat metrics exhibit differential sensitivities to tissue damage in MS white matter, they can be collected in combination to provide an efficient, comprehensive measure of myelin water and macromolecular pool proton signals. These complementary measures may offer a more sensitive, non-invasive biopsy of early precursor signals in NAWM that occur prior to lesion formation. They may also aid in monitoring the efficacy of remyelination therapies.

Probabilistic magnetometry with a two-spin system in diamond

Solid-state magnetometers like the nitrogen-vacancy (NV) center in diamond have been of paramount importance for the development of quantum sensing with nanoscale spatial resolution. The underlying protocol is a Ramsey sequence, that imprints an external static magnetic field into the phase of the quantum sensor, which is subsequently read out. In this theoretical work we propose a sensing scheme that harnesses the hyperfine coupling between the NV center and a nearby nuclear spin to set a post-selection protocol. We show that concentrating valuable sensing information into a single successful measurement yields an improvement in sensitivity over Ramsey in the range of short transverse relaxation times. By considering realistic experimental conditions, we found that the detection of weak magnetic fields in the μT range can be achieved with a sensitivity of few tens of nTHz−1/2 at cryogenic temperature (4 K), and μTHz−1/2 at room temperature.

Research progress of <sup>10</sup>B concentration and distribution measurement in boron neutron capture therapy

Boron neutron capture therapy (BNCT) is a dual tumor radiotherapy method combining boron-10 containing drugs and heavy ion therapy, which can kill cancer cells with almost no damage to normal cells, and achieve precise cell-scale treatment. However, the BNCT does not really enter into clinical application stage though it has been developed for nearly 70 years. The methods of measuring the concentration distribution of boron-10 containing drugs in vivo cannot meet the clinical needs, which is one of the core problems affecting the effect and safety of clinical application of BNCT. This article reviews the current methods of measuring the concentration distribution of boron-10 drugs, including the invasive estimation methods that have been used in clinical practice, the researching single photon emission tomography (SPECT) method, positron emission tomography (PET) method, nuclear magnetic resonance (NMR) method, etc., and analyzes the advantages and limitations of current methods. Based on the characteristics of the low gyromagnetic ratio of the boron-10 element and the extremely short magnetic resonance transverse relaxation time, the research ideas of ultra-short echo time magnetic resonance boron-10 quantitative imaging are proposed. The feasibility of quantitative measurement of boron-10 distribution in vivo based on ultrashort echo time magnetic resonance imaging is analyzed theoretically.

Assessment of mechanical properties of articular cartilage with quantitative three-dimensional ultrashort echo time (UTE) cones magnetic resonance imaging

Conventional magnetic resonance imaging (MRI) is not capable of detecting signal from the deep cartilage due to its short transverse relaxation time (T2). Moreover, several quantitative MRI techniques are significantly influenced by the magic angle effect. The combinations of ultrashort echo time (UTE) MRI with magnetization transfer (UTE-MT) and Adiabatic T1ρ (UTE-AdiabT1ρ) imaging allow magic angle-insensitive assessments of all regions of articular cartilage. The purpose of this study was to investigate the correlations between quantitative three-dimensional UTE MRI biomarkers and mechanical properties of human tibiofemoral cartilage specimens. In total, 40 human tibiofemoral cartilage specimens were harvested from three male and four female donors (64 ± 18 years old). Cartilage samples were scanned using a series of quantitative 3D UTE Cones T2* (UTE-T2*), T1 (UTE-T1), UTE-AdiabT1ρ, and UTE-MT sequences in a standard knee coil on a clinical 3T scanner. UTE-MT data were acquired with a series of MT powers and frequency offsets to calculate magnetization transfer ratio (MTR), as well as macromolecular fraction (MMF) and macromolecular T2 (T2mm) through modeling. Cartilage stiffness and Hayes elastic modulus were measured using indentation tests. Correlations of 3D UTE Cones MRI measurements in the superficial layer, deep layer, and global regions of interest (ROIs) with mechanical properties were investigated. Cartilage mechanical properties demonstrated highest correlations with UTE measures of the superficial layer of cartilage. AdiabT1ρ, MTR, and MMF in superficial layer ROIs showed significant correlations with Hayes elastic modulus (p < 0.05, R = −0.54, 0.49, and 0.66, respectively). These UTE measures in global ROIs showed significant, though slightly lower, correlations with Hayes elastic modulus (p < 0.05, R = −0.37, 0.52, and 0.60, respectively). Correlations between other UTE MRI measurements (T2*, T1, and T2mm) and mechanical properties were non-significant. The 3D UTE-AdiabT1ρ and UTE-MT sequences were highlighted as promising surrogates for non-invasive assessment of cartilage mechanical properties. MMF from UTE-MT modeling showed the highest correlations with cartilage mechanics.

Pulse sequences for measuring exchange rates between proton species: From unlocalised NMR spectroscopy to chemical exchange saturation transfer imaging

Within the field of NMR spectroscopy, the study of chemical exchange processes through saturation transfer techniques has a long history. In the context of MRI, chemical exchange techniques have been adapted to increase the sensitivity of imaging to small fractions of exchangeable protons, including the labile protons of amines, amides and hydroxyls. The MR contrast is generated by frequency-selective irradiation of the labile protons, which results in a reduction of the water signal associated with transfer of the labile protons’ saturated magnetization to the protons of the surrounding free water. The signal intensity depends on the rate of chemical exchange and the concentration of labile protons as well as on the properties of the irradiation field. This methodology is referred to as CEST (chemical exchange saturation transfer) imaging. Applications of CEST include imaging of molecules with short transverse relaxation times and mapping of physiological parameters such as pH, temperature, buffer concentration and chemical composition due to the dependency of this chemical exchange effect on all these parameters. This article aims to describe these effects both theoretically and experimentally. In depth analysis and mathematical modelling are provided for all pulse sequences designed to date to measure the chemical exchange rate. Importantly, it has become clear that the background signal from semi-solid protons and the presence of the Nuclear Overhauser Effect (NOE), either through direct dipole-dipole mechanisms or through exchange-relayed signals, complicates the analysis of CEST effects. Therefore, advanced methods to suppress these confounding factors have been developed, and these are also reviewed. Finally, the experimental work conducted both in vitro and in vivo is discussed and the progress of CEST imaging towards clinical practice is presented.

Magnetic Resonance Imaging of Hard Tissues and Hard Tissue Engineered Bio-substitutes

Magnetic resonance imaging (MRI) is a non-invasive diagnostic imaging tool based on the detection of protons into the tissues. This imaging technique is remarkable because of high spatial resolution, strong soft tissue contrast and specificity, and good depth penetration. However, MR imaging of hard tissues, such as bone and teeth, remains challenging due to low proton content in such tissues as well as to very short transverse relaxation times (T2). To overcome these issues, new MRI techniques, such as sweep imaging with Fourier transformation (SWIFT), ultrashort echo time (UTE) imaging, and zero echo time (ZTE) imaging, have been developed for hard tissues imaging with promising results reported. Within this article, MRI techniques developed for the detection of hard tissues, such as bone and dental tissues, have been reviewed. The main goal was thus to give a comprehensive overview on the corresponding (pre-) clinical applications and on the potential future directions with such techniques applied. In addition, a section dedicated to MR imaging of novel biomaterials developed for hard tissue applications was given as well.

The logging recognition of solid bitumen and its effect on physical properties, AC, resistivity and NMR parameters

Abstract Solid bitumen not only strongly damages the reservoir properties, but it is easily confused with oil and gas in the conventional classification logging interpretation, which seriously affects the effective recognition of oil and gas. Thus, it leads to a deceptive estimation of the reserve. Focusing on the above problems, this study takes Jurassic solid bitumen-containing reservoirs from the Santai-Northern Santai area in the Junggar Basin as an example, and aims to quantitatively evaluate the impact of solid bitumen on the porosity, permeability, resistivity, AC (Acoustic) and NMR (Nuclear Magnetic Resonance), with a comparison between the values of these parameters before and after core bitumen dissolution, as well as to establish an NMR identification method for solid bitumen. The results show that solid bitumen can damage the pore structure of the reservoir and cause a reduction of porosity and permeability. The content of solid bitumen is linearly correlated with the change of porosity and permeability. After solid bitumen dissolved, the resistivity decreased, the longitudinal wave time difference (Vp) and shear wave time difference (Vs) increased, and the shear wave time difference changed noticeably. The content of solid bitumen is exponentially correlated with the change of resistivity, and linearly correlated with the change of longitudinal wave time difference and shear wave time difference. Solid bitumen had a short transverse relaxation time and a response range of 10–1000 μs (Peak 1) on the T2 map. Bitumen-containing sandstone had 3 peaks on the T2 map. Peak 1 decreased, while Peaks 2 and 3 increased after the solid bitumen dissolved. Solid bitumen can be characterized by a typical short time lag of the transverse wave, a bigger density porosity than the NMR porosity and small values of T1LM and T2LM, which led to an effective recognition of the layers of solid bitumen. The results are significant for the exploration and development of oilfields.