Fast T1 mapping of the brain at high field using Look-Locker and fast imaging

This study aims to develop and evaluate a new method for fast high resolution T1 mapping of the brain based on the Look-Locker technique. Single-shot turboflash sequence with high temporal acceleration is used to sample the recovery of inverted magnetization. Multi-slice interleaved acquisition within one inversion slab is used to reduce the number of inversion pulses and hence SAR. Accuracy of the proposed method was studied using simulation and validated in phantoms. It was then evaluated in healthy volunteers and stroke patients. In-vivo results were compared to values obtained by inversion recovery fast spin echo (IR-FSE) and literatures. With the new method, T₁ values in phantom experiments agreed with reference values with median error < 3%. For in-vivo experiments, a T1 map was acquired in 3.35 s and the T1 maps of the whole brain were acquired in 2 min with two-slice interleaving, with a spatial resolution of 1.1 × 1.1 × 4 mm³. The T₁ values obtained were comparable to those measured with IR-FSE and those reported in literatures. These results demonstrated the feasibility of the proposed method for fast T1 mapping of the brain in both healthy volunteers and stroke patients at 3T.     

Improved spectral quality for 3D MR spectroscopic imaging using a high spatial resolution acquisition strategy

Spectral quality in (1)H MR spectroscopic imaging (MRSI) of the brain is often significantly degraded in regions subject to local magnetic susceptibility variations, which results in broadened and distorted spectral lineshapes. In this report, a modified acquisition strategy for volumetric echo-planar spectroscopic imaging (3D EPSI) is presented that extends the region of the brain that can be observed. The data are sampled at higher spatial resolution, then corrected for local B(0) shifts and reconstructed such that the final spatial resolution matches that of 3D EPSI data acquired with the conventional lower spatial resolution. Comparison of in vivo data obtained at 1.5 T with these two acquisition schemes shows that the high spatial resolution acquisition provides considerable reduction of spectral linewidths in many problematic brain regions, though with a reduction in signal-to-noise ratio by a factor of approximately 1.4 to 1.6 for the matrix sizes used in this study. However, the effect of the increased noise was largely offset by the improved spectral quality, leading to an overall improvement of the metabolite image quality obtained using automated spectral analysis.     

Depth map resolution improvement for 3D range-intensity correlation laser imaging

This Letter proposes a high bit-depth coding method to improve depth map resolution and render it suitable to human-eye observation in 3D range-intensity correlation laser imaging. In this method, a high bit-depth CCD camera with a nanosecond-scaled gated intensifier is used as an image sensor; subsequently two high bit-depth gate images with specific range-intensity profiles are obtained to establish the gray depth map and finally the gray depth map is encoded by an equidensity pseudocolor. With this method, a color depth map is generated with higher range resolution. In our experimental work, the range resolution of the depth map is improved by a factor of 1.67.     

STRAFI imaging of solids: The spatial resolution for quadrupolar nuclei withI=3/2

The density matrix formalism has been used for computer calculations of the thickness of the excited slice, which determines the spatial resolution, in the case of quadrupolar nuclei havingI=3/2, for varying values of the electric quadrupolar coupling constant and the pulse-duration, when the spins are placed in a very strong magnetic field-gradient (50 T/m).     

Extreme ultraviolet radiation for coherent diffractive imaging with high spatial resolution

Using different noble gases,argon,neon and helium,we are able to generate by high-harmonic generation(HHG) just a few harmonic orders in the spectral range 10-35 nm with a photon flux of～2.10 12 photons/(harmonic cm2 s) for argon and～10 10 photons/(harmonic cm2 s) for helium. The few-harmonic-order radiation is used for coherent diffractive imaging directly without any spectral filter. A spatial resolution of～100 nm is achieved using a～30 nm HHG source.     

Optimization of 3D MP-RAGE for neonatal brain imaging at 3.0 T

Three-dimensional (3D) magnetic resonance imaging (MRI) has shown great potential for studying the impact of prematurity and pathology on brain development. We have investigated the potential of optimized T1-weighted 3D magnetization-prepared rapid gradient-echo imaging (MP-RAGE) for obtaining contrast between white matter (WM) and gray matter (GM) in neonates at 3 T. Using numerical simulations, we predicted that the inversion time (TI) for obtaining strongest contrast at 3 T is approximately 2 s for neonates, whereas for adults, this value is approximately 1.3 s. The optimal neonatal TI value was found to be insensitive to reasonable variations of the assumed T1 relaxation times. The maximum theoretical contrast for neonates was found to be approximately one third of that for adults. Using the optimized TI values, MP-RAGE images were obtained from seven neonates and seven adults at 3 T, and the contrast-to-noise ratio (CNR) was measured for WM versus five GM regions. Compared to adults, neonates exhibited lower CNR between cortical GM and WM and showed a different pattern of regional variation in CNR. These results emphasize the importance of sequence optimization specifically for neonates and demonstrate the challenge in obtaining strong contrast in neonatal brain with T1-weighted 3D imaging.     

Knee osteochondral junction imaging using a fast 3D T1-weighted ultrashort echo time cones sequence at 3T

The osteochondral junction (OCJ) of the knee joint is comprised of multiple tissue components, including a portion of the deep layer cartilage, calcified cartilage, and subchondral bone. The OCJ is of increasing radiological interest as it may be relevant in the early pathogenesis of osteoarthritis (OA). Due to its short transverse relaxation, the OCJ is invisible to clinical MR sequences. The purpose of this study was to develop a fast 3D T₁-weighted ultrashort echo time cones sequence with fat saturation (FS-UTE-Cones) for high resolution and high contrast imaging of the OCJ on a clinical 3T scanner. First, numerical simulations were performed to investigate how the flip angle affected the signal intensities and contrasts of both short and long T₁ tissues. The results from these simulations demonstrated that higher short T₁ contrast could be achieved with higher flip angle. Next, T₁ relaxation was measured for the different layers of a human patellar cartilage sample, and the results showed that the deepest layer had a significantly shorter T₁ value than other layers. Finally, a healthy knee joint was scanned with different flip angles and the OCJ was highlighted in the T₁-weighted FS-UTE-Cones sequence using a flip angle greater than 20°. The clinical T₂-weighted and proton density-weighted FSE sequences were also included for comparison, revealing a dark OCJ region. Representative T₁-weighted FS-UTE-Cones images of the whole knee of a healthy volunteer showed high signal intensity bands in the OCJ regions of the patella, femur, and tibia. On the other hand, T₁-weighted FS-UTE-Cones imaging of the knee joints of OA patients revealed regions with reduction or loss of these high signal intensity bands in the OCJ regions, indicating abnormal OCJ tissue composition. The proposed 3D T₁-weighted FS-UTE-Cones sequence with a 3-min scan time may be very useful for demonstrating the involvement of the OCJ regions in early OA.     

Fast 3D spatial EPR imaging using spiral magnetic field gradient

Electron paramagnetic resonance imaging (EPRI) provides direct detection and mapping of free radicals. The continuous wave (CW) EPRI technique, in particular, has been widely used in a variety of applications in the fields of biology and medicine due to its high sensitivity and applicability to a wide range of free radicals and paramagnetic species. However, the technique requires long image acquisition periods, and this limits its use for many in vivo applications where relatively rapid changes occur in the magnitude and distribution of spins. Therefore, there has been a great need to develop fast EPRI techniques. We report the development of a fast 3D CW EPRI technique using spiral magnetic field gradient. By spiraling the magnetic field gradient and stepping the main magnetic field, this approach acquires a 3D image in one sweep of the main magnetic field, enabling significant reduction of the imaging time. A direct one-stage 3D image reconstruction algorithm, modified for reconstruction of the EPR images from the projections acquired with the spiral magnetic field gradient, was used. We demonstrated using a home-built L-band EPR system that the spiral magnetic field gradient technique enabled a 4-7-fold accelerated acquisition of projections. This technique has great potential for in vivo studies of free radicals and their metabolism.     

Linear Response Equilibrium versus echo-planar encoding for fast high-spatial resolution 3D chemical shift imaging

In this work Linear Response Equilibrium (LRE) and Echo-planar spectroscopic imaging (EPSI) are compared in terms of sensitivity per unit time and power deposition. In addition an extended dual repetition time scheme to generate broad stopbands for improved inherent water suppression in LRE is presented. The feasibility of LRE and EPSI for assessing cholesterol esters in human carotid plaques with high spatial resolution of 1.95×1.15×1.15 mm(3) on a clinical 3T MR system is demonstrated. In simulations and phantom experiments it is shown that LRE has comparable but lower sensitivity per unit time relative to EPSI despite stronger signal generated. This relates to the lower sampling efficiency in LRE relative to EPSI as a result of limited gradient performance on clinical MR systems. At the same time, power deposition of LRE is significantly reduced compared to EPSI making it an interesting niche application for in vivo high field spectroscopic imaging of metabolites within a limited bandwidth.     

Comparison of T1-weighted spin-echo and 3D T1-weighted multi-shot Echo Planar pulse sequences in imaging the brain at it.

The purpose of this study was to evaluate the ability of three dimensional T1-weighted multi-shot Echo Planar Imaging (3D T1w EPI) MR pulse sequence to provide comparable to T1w Spin Echo (SE) results in various diseases of the brain, during shorter acquisition times. Thirty-six patients (aged 30-74 years) with various indications were included in the study. All examinations were performed with a 1T MR scanner with a maximum gradient strength of 15 mT/m. The SE sequence lasted 3 min 50s and the 3D T1w EPI 59s. The quantitative analysis included number of enhancing lesions, signal-to-noise ratio of the enhancing lesions and contrast-to-noise ratio (CNR) between enhancing lesions and white matter in both sequences before and after i.v. administration of 0.1 mmol/kg gadopentetate dimeglumine. In addition, the percentage increase of enhancement was measured in each lesion of each sequence. The qualitative analysis included a) conspicuity of the lesions and b) presence of artifacts. The T1w SE sequence was significantly better compared to 3D T1w EPI in all quantitative measurements with the exception of CNR of enhancing lesions before contrast administration and the percentage enhancement. The conspicuity of the lesions did not differ between the two sequences. The EPI sequence presented with significantly more artifacts. We conclude that the 3D T1w EPI sequence could not be used instead of the conventional T1w SE, in routine imaging of the brain. Its overall diagnostic capability, could be useful only in uncooperative patients.     

High spatial resolution in vivo 2D (1)H magnetic resonance spectroscopic imaging of human muscles with a band-selective technique.

This report demonstrates a 2D (1)H magnetic resonance spectroscopic imaging (MRSI) technique that can address some technical difficulties often encountered in MRS studies of human muscles. A preliminary application of this whole-slice technique in human skeletal muscles demonstrates clearly noticeable differences in (1)H metabolite spectra between different human muscles. This observation illustrates the importance of multi-voxel and high spatial resolution in a heterogeneous environment. This technique is robust, can be easily implemented on a commercial MR scanner, and should prove useful for investigators in both basic and clinical (1)H MRS studies.     

Development of high resolution 3D hyperpolarized carbon-13 MR molecular imaging techniques

The goal of this project was to develop and apply techniques for T₂ mapping and 3D high resolution (1.5 mm isotropic; 0.003 cm³) ¹³C imaging of hyperpolarized (HP) probes [1-¹³C]lactate, [1-¹³C]pyruvate, [2-¹³C]pyruvate, and [¹³C,¹⁵N₂]urea in vivo. A specialized 2D bSSFP sequence was implemented on a clinical 3T scanner and used to obtain the first high resolution T₂ maps of these different hyperpolarized compounds in both rats and tumor-bearing mice. These maps were first used to optimize timings for highest SNR for single time-point 3D bSSFP acquisitions with a 1.5 mm isotropic spatial resolution of normal rats. This 3D acquisition approach was extended to serial dynamic imaging with 2-fold compressed sensing acceleration without changing spatial resolution. The T₂ mapping experiments yielded measurements of T₂ values of > 1 s for all compounds within rat kidneys/vasculature and TRAMP tumors, except for [2-¹³C]pyruvate which was ~ 730 ms and ~ 320 ms, respectively. The high resolution 3D imaging enabled visualization the biodistribution of [1-¹³C]lactate, [1-¹³C]pyruvate, and [2-¹³C]pyruvate within different kidney compartments as well as in the vasculature. While the mouse anatomy is smaller, the resolution was also sufficient to image the distribution of all compounds within kidney, vasculature, and tumor. The development of the specialized 3D sequence with compressed sensing provided improved structural and functional assessments at a high (0.003 cm³) spatial and 2 s temporal resolution in vivo utilizing HP ¹³C substrates by exploiting their long T₂ values. This 1.5 mm isotropic resolution is comparable to ¹H imaging and application of this approach could be extended to future studies of uptake, metabolism, and perfusion in cancer and other disease models and may ultimately be of value for clinical imaging.     

Enhancement of spatial resolution of ghost imaging via localizing and thresholding

In ghost imaging, an illumination light is split into test and reference beams which pass through two different optical systems respectively and an image is constructed with the second-order correlation between the two light beams. Since both light beams are diffracted when passing through the optical systems, the spatial resolution of ghost imaging is in general lower than that of a corresponding conventional imaging system. When Gaussian-shaped light spots are used to illuminate an object, randomly scanning across the object plane, in the ghost imaging scheme, we show th√at by localizing central positions of the spots of the reference light beam, the resolution can be increased by a factor of 2~(1/2) same as that of the corresponding conventional imaging system. We also find that the resolution can be further enhanced by setting an appropriate threshold to the bucket measurement of ghost imaging.     

非等分辨率光线跟踪体绘制方法及其在超声CT三维成像中的应用

光线跟踪绘制是获得广泛应用的三维标量场数据的计算机可视化方法之一,它所处理的数据量之大要求数据压缩存放.本文推导了非等分辨率条件下数据压缩存贮时直角坐标系中的广义的射线方程及链式关系,研究了它在基于CT切片的超声三维成像中的应用.实例表明,该方法能够真实反映原始数据特征,即,对于大尺度物体(相对于换能器声场分辨率),该方法能够得到清晰的图像,而对于小尺度物体,由于原数据分辨率不够导致图像模糊,但是该方法仍然能够定性表明缺陷的存在.     

3D sensitivity encoded ellipsoidal MR spectroscopic imaging of gliomas at 3T

Purpose

The goal of this study was to implement time efficient data acquisition and reconstruction methods for 3D magnetic resonance spectroscopic imaging (MRSI) of gliomas at a field strength of 3T using parallel imaging techniques.

Methods

The point spread functions, signal to noise ratio (SNR), spatial resolution, metabolite intensity distributions and Cho:NAA ratio of 3D ellipsoidal, 3D sensitivity encoding (SENSE) and 3D combined ellipsoidal and SENSE (e-SENSE) k-space sampling schemes were compared with conventional k-space data acquisition methods.

Results

The 3D SENSE and e-SENSE methods resulted in similar spectral patterns as the conventional MRSI methods. The Cho:NAA ratios were highly correlated (P<.05 for SENSE and P<.001 for e-SENSE) with the ellipsoidal method and all methods exhibited significantly different spectral patterns in tumor regions compared to normal appearing white matter. The geometry factors ranged between 1.2 and 1.3 for both the SENSE and e-SENSE spectra. When corrected for these factors and for differences in data acquisition times, the empirical SNRs were similar to values expected based upon theoretical grounds. The effective spatial resolution of the SENSE spectra was estimated to be same as the corresponding fully sampled k-space data, while the spectra acquired with ellipsoidal and e-SENSE k-space samplings were estimated to have a 2.36–2.47-fold loss in spatial resolution due to the differences in their point spread functions.

Conclusion

The 3D SENSE method retained the same spatial resolution as full k-space sampling but with a 4-fold reduction in scan time and an acquisition time of 9.28 min. The 3D e-SENSE method had a similar spatial resolution as the corresponding ellipsoidal sampling with a scan time of 4:36 min. Both parallel imaging methods provided clinically interpretable spectra with volumetric coverage and adequate SNR for evaluating Cho, Cr and NAA.     

Analysis of the Look-Locker T(1) mapping sequence in dynamic contrast uptake studies: simulation and in vivo validation

An alternative to the pulse sequences at present used in dynamic contrast uptake MRI is the dynamic LL-EPI T(1) mapping method. This method generates T(1) estimates in a few seconds, thereby allowing dynamic studies. A particular advantage of the LL-EPI technique is that it provides the opportunity to generate spatial and temporal information about the paramagnetic contrast agent concentration independently of the inflow rate. This paper illustrates, by computer simulations, the accuracy of the estimated 1/T(1) value when using the LL-EPI technique in situations that are not supported by the model. The simulated situations not supported by the model are those in which the longitudinal and transversal relaxation rates change during the T(1) mapping. The most critical moment occurs during a bolus passage of contrast agent when the concentration gradient is large. The computer simulations of the LL-EPI T(1) mapping method in non-supported situations show that in normal perfused capillary tissue the error in the estimated 1/T(1) value is within the absolute error of 0.1 s(-1) in most simulated situations, although in a typical vessel the simulations do indicate that the stated absolute error tolerance of 0.5 s(-1) is exceeded relatively easily. However, this transgression can be rectified by a non-bolus injection of the contrast agent media.     

High-peak-power,single-mode,nanosecond pulsed,all-fiber laser for high resolution 3D imaging LIDAR system

This study presents an eye-safe, single-mode, nanosecond-pulsed, and all-fiber laser source with master- oscillator-power-amplifier configuration at 1 550 nm that is suitable for high-resolution three-dimensional (3D) imaging light detection and ranging (LIDAR) system. The output peak power of 7.6 kW is obtained at the 1.2-ns pulse width and 50-kHz repetition rate. The single-mode pulse laser output ensures the range precision and imaging results of the LIDAR system. The laser is used as a transmitter for the 3D imaging LIDAR system. The detailed characteristics of the LIDAR system and the results of the 3D imaging are presented.     

High spatial resolution imaging in a clipping Kagomé lattice photonic crystal

In this paper, a two-dimensional Kagomé lattice photonic crystal (PC) made of GaAs (ɛ = 12.96) dielectric rods in air is considered. This Kagomé lattice PC has an effective refractive index n_eff = −1 at a low normalized frequency ω = 0.187 × 2πc/a. Imaging quality and the capability of the super-resolution of two point sources are studied for a superlens made of such PC structure. In order to achieve a high quality image and to improve the spatial super-resolution of two sources, a clipping Kagomé lattice PC is designed. Results simulated by finite-difference time-domain method show that imaging quality and super-resolution of two sources can be enhanced greatly as the perfect Kagomé lattice structure are superseded by the clipping Kagomé lattice structure. Coupled-mode theory analysis gives an explanation why the clipping structure is superior to the perfect one for both the imaging quality and the capability of the super-resolution of two sources. This clipping Kagomé lattice PC structure would be widely used in optical devices and integrated circuit.     

Sequential method for high 3-D resolution imaging in nuclear medicine

A sequential method is developed to obtain a high resolution 3-D image distribution of the activity of a radioactive tracer. Two different types of reconstruction are presented. The first method, related to X or γ ray motion tomography, yields reconstructed objects slices (tomograms) containing superimposed out-of-focus blurred planes. The second method, utilizing computer processing, generates each plane (slice) separately, free from out-of-focus images, as in X-ray scanner transaxial tomography. This approach avoids calculations of the tomograms and improves the restitution of low spatial frequencies. A method of spatial filtering for quantum noise reduction is also proposed.     

A high spatial resolution 1H magnetic resonance spectroscopic imaging technique for breast cancer with a short echo time

The high sensitivity but low specificity of breast MRI has prompted exploration of breast (1)H MRS for breast cancer detection. However, several obstacles still prevent the routine application of in vivo breast (1)H MRS, including poor spatial resolution, long acquisition time associated with conventional multi-voxel MRS imaging (MRSI) techniques, and the difficulty of "extra" lipid suppression in a magnetic field with relatively poor achievable homogeneity compared to the brain. Using a combination of a recently developed echo-filter (EF) suppression technique and an elliptical sampling scheme, we demonstrate the feasibility of overcoming these difficulties. It is robust (the suppression technique is insensitive to magnetic field inhomogeneity), fast (acquisition time of about 12 min) and offers high spatial resolution (up to 0.6 cm(3) per voxel at 1.5 T with a TE of only 60 ms). This approach should be even better at 3 T with higher resolution and/or shorter TE.