Visualization of liver uptake function using the uptake contrast-enhanced ratio in hepatobiliary phase imaging

Purpose

To visualize liver uptake function using the uptake contrast-enhanced ratio in hepatobiliary phase (uptake CERH) magnetic resonance imaging.

Materials and methods

Thirty-seven patients with hepatocellular carcinoma (HCC) and 23 with metastatic liver cancer were evaluated. Hepatobiliary phase images were acquired 20 min after an intravenous bolus injection of gadoxetic acid disodium. We assumed that the contrast-enhanced ratio in the hepatobiliary phase (CERH) in the spleen was similar to the contrast-enhanced ratio in the extracellular matrix (CEREM). The Uptake CERH value was defined as the percentage signal gain between the precontrast and hepatobiliary phase images (without CEREM). The Uptake CERH value measured the tumor-free liver parenchyma. The association of the uptake CERH value with the biochemical liver function test results, and hepatocellular density in the liver parenchyma was assessed. Correlations were examined using Pearson correlation coefficient and the Mann–Whitney test.

Results

The uptake CERH value was correlated with albumin, bilirubin, indocyanine green retention rate at 15 min, prothrombin activity(%), platelet count, and cellular density in the liver parenchyma (p < 0.01).

Conclusions

Uptake CERH images are useful for visualizing liver uptake function.     

Relaxation effects in the quantification of fat using gradient echo imaging

Quantification of fat has been investigated using images acquired from multiple gradient echoes. The evolution of the signal with echo time and flip angle was measured in phantoms of known fat and water composition and in 21 research subjects with fatty liver. Data were compared to different models of the signal equation, in which each model makes different assumptions about the T1 and/or T2* relaxation effects. A range of T1, T2*, fat fraction and number of echoes was investigated to cover situations of relevance to clinical imaging. Results indicate that quantification is most accurate at low flip angles (to minimize T1 effects) with a small number of echoes (to minimize spectral broadening effects). At short echo times, the spectral broadening effects manifest as a short apparent T2 for the fat component.     

装置极化效率对极化中子成像质量的影响及修正分析

极化中子照相技术通过分析极化中子束的自旋相移对样品磁场进行成像, 自旋极化/分析装置是照相系统的主要组成部分. 引入中子自旋极化/分析装置的极化效率参数, 从中子极化矢量与磁场相互作用机理出发, 重新推导探测中子强度与磁场分布的定量关系, 利用谱仪模拟软件VITESS, 选取bender型超镜极化器和 ³He 自旋过滤器作为极化/分析装置, 对量化修正式进行验证, 并综合装置极化效率、单色器能量分辨精度和bender型极化器的几何结构等参数, 初步分析极化中子照相技术的磁场定量检测能力, 相关结果可为极化中子照相的实验数据处理技术研究及装置设计提供参考. 关键词： 极化效率 中子照相 磁场成像     

Isotope effects in water as investigated by neutron diffraction and path integral molecular dynamics

The structures of heavy and light water at 300?K were investigated by using a joint approach in which the method of neutron diffraction with oxygen isotope substitution was complemented by path integral molecular dynamics simulations. The diffraction results, which give intra-molecular O-D and O-H bond distances of 0.985(5) and 0.990(5)??, were found to be in best agreement with those obtained by using the flexible anharmonic TTM3-F water model. Both techniques show a difference of ??0.5% between the O-D and O-H intra-molecular bond lengths, and the results support a competing quantum effects model for water in which its structural and dynamical properties are governed by an offset between intra-molecular and inter-molecular quantum contributions. Further consideration of the O-O correlations is needed in order to improve agreement with experiment.     

B模式实时成像定量监控超声空化时空行为的研究

提出一种采用B超图像实现高强聚焦超声(HIFU)治疗时声空化的时空量化监控的方法。首先,采用B模式实时成像系统对不同声辐照能量下的HIFU在凝胶仿体中引发的超声空化进行实验监测;接着,利用二维数字图像处理算法消除高强聚焦超声(HIFU)在B超图像中产生的干涉条纹,并在此基础上,对B超成像中观察到的高亮区域的面积变化情况进行量化分析;最后,进一步讨论了驱动声压或脉冲宽度对超声空化产生的高亮区域的生成速度和面积大小的影响。结果显示该方法可以有效去除B超图像中的干涉条纹,并对HIFU引发的空化现象进行实时监测。实验结果还表明辐照声能量的提高将引发更强烈的声空化行为,并且显著缩短HIFU引发的空化泡群的初始生成时间。研究结果对进一步优化HIFU治疗有重要意义。     

B模式实时成像定量监控超声空化时空行为的研究

提出一种采用B超图像实现高强聚焦超声(HIFU)治疗时声空化的时空量化监控的方法。首先,采用B模式实时成像系统对不同声辐照能量下的HIFU在凝胶仿体中引发的超声空化进行实验监测;接着,利用二维数字图像处理算法消除高强聚焦超声(HIFU)在B超图像中产生的干涉条纹,并在此基础上,对B超成像中观察到的高亮区域的面积变化情况进行量化分析;最后,进一步讨论了驱动声压或脉冲宽度对超声空化产生的高亮区域的生成速度和面积大小的影响。结果显示该方法可以有效去除B超图像中的干涉条纹,并对HIFU引发的空化现象进行实时监测。实验结果还表明辐照声能量的提高将引发更强烈的声空化行为,并且显著缩短HIFU引发的空化泡群的初始生成时间。研究结果对进一步优化HIFU治疗有重要意义。     

Visualization of lipid-receptor interactions on single cells by time-resolved imaging fluorescence microscopy

The physical interaction between plasma-membrane lipids and the epidermal growth factor (EGF)-receptor was investigated on single A431 human epidermoid carcinoma cells by monitoring fluorescence resonance energy transfer (FRET) between exogeneously added fluorescein-EGF (donor) and 2-(4,4-difluoro-5,7-dimethyl-4-bora-3a,4a-diaza-s-indacene-3-pentanoyl)-1-hexadecanoyl-sn-glycero-3-phosphocholine (Bodipy-PC, acceptor) using donor-photobleaching FRET-microscopy. The measured mean FRET-efficiency of 13% is indicative of such a physical interaction and exemplifies the great potential and sensitivity of time-resolved imaging fluorescence microscopy techniques for the study of lipid-receptor interactions on single cells.     

Non-destructive quantification of pharmaceutical tablet coatings using terahertz pulsed imaging and optical coherence tomography

Optical coherence tomography (OCT) and terahertz pulsed imaging (TPI) are two powerful techniques allowing high quality cross-sectional images from within scattering media to be obtained non-destructively. In this paper, we report experimental results of using OCT and TPI for quantitatively characterizing pharmaceutical tablet coatings in the thickness range of 10-140 μm. We found that the spectral OCT system developed in-house has an axial resolution of 0.9 μm, and is capable of quantifying very thin coatings in the range of 10-60 μm. The upper limit of 60 μm within the tablet coating and core is owed to the strong scattering of OCT light, which has relatively short wavelengths in the range of 0.5-1.0 μm. On the other hand, TPI utilizes terahertz radiation that has substantially long wavelengths in the range of hundreds of microns, and thus is less prone to the scattering problem. Consequently TPI has been demonstrated to be able to quantify thicker coatings in the range of 40-140 μm and beyond. We concluded that OCT and TPI are two complementary analytical techniques for non-destructive and quantitative characterization of pharmaceutical tablet coatings.     

Practical effects of pressure-transmitting media on neutron diffraction experiments using Paris–Edinburgh presses

ABSTRACT

To understand the practical effects of pressure-transmitting media (PTM) on neutron diffraction using Paris–Edinburgh presses, diffraction patterns of MgO were collected to approximately 20?GPa using PTMs of Pb, AgCl, 4:1 methanol–ethanol (ME) mixture with and without heating, N₂, and Ar. Hydrostaticity in the sample chamber estimated from the MgO 220 peak width improves in the order of Pb, AgCl, Ar, ME mixture, N₂, and the heated ME mixture. Unlike previous results using diamond anvil cells, the unheated ME mixture is superior to Ar even after freezing, probably due to the cup on the anvil face. Considering these results and the sizable coherent scattering of Ne, which would show good hydrostaticity, we conclude that the ME mixture (preferably the heated one) is the best PTM in neutron experiments up to 20?GPa, while Ar can be substituted when a sample is reactive to alcohols.     

Detection of water surface capillary wave by analysis of turning-point local signal data using a laser interferometer

A laser interferometry technique is developed to detect water surface capillary waves caused by an impinging acoustic pressure field. The frequency and amplitude of the water surface capillary waves can be estimated from the local signal data at some special points of the phase modulated interference signal, which is called the turning points. Demodulation principles are proposed to explain this method. Experiments are conducted under conditions of different intensity and different frequency driving acoustic signals. The results show the local signal data analysis can effectively estimate the amplitude and frequency of water surface capillary waves.     

Structure of water in mesoporous organosilica by calorimetry and inelastic neutron scattering

In this paper, we describe the preparation of mesoporous organosilica samples with hydrophilic or hydrophobic organic functionality inside the silica channel. We synthesized mesoporous organosilica of identical pore sizes based on two different organic surface functionality namely hydrophobic (based on octyltriethoxysilane OTES) and hydrophilic (3-aminopropyltriethoxysilane ATES) and MCM-41 was used as a reference system. The structure of water/ice in those porous silica samples have been investigated over a range temperatures by differential scanning calorimetry (DSC) and inelastic neutron scattering (INS). INS study revealed that water confined in hydrophobic mesoporous organosilica shows vibrational behavior strongly different than bulk water. It consists of two states: water with strong and weak hydrogen bonds (with ratio 1:2.65, respectively), compared to ice-Ih. The corresponding O-O distances in these water states are 2.67 and 2.87 ?, which strongly differ compared to ice-Ih (2.76 ?). INS spectra for water in hydrophilic mesoporous organosilica ATES show behavior similar to bulk water, but with greater degree of disorder.     

Characterization of natural resin materials using water adsorption and various advanced techniques

A physicochemical characterization of natural raw resin material was evaluated and reported. The studied material is a natural resin, a natural product from pinus halepensis trees which is collected from the forests of Chalkidiki region of North Greece. The plurality of this product combined with its special property of removing water from commercial liquid fuels commands the detailed physicochemical characterization of this material. In particular, various techniques, such as water adsorption at 22 °C, thermogravimetric analysis, differential scanning calorimetry, Fourier transform infrared spectroscopy and X-ray diffraction, were used in order to evaluate the structural and surface properties of the material. The water adsorption isotherm was also measured and fitted using the Guggenheim, Anderson and De Boer model in order to correlate the water activity characteristics. In addition, the kinetics of the adsorption was also fitted with good accuracy using the exponential Chapman model. Furthermore, as the results show, the natural resin presents good thermal characteristics. Finally, the studied material presents efficient water adsorption properties, up to 246.8 mmol/g, and it can be proposed as a promising dehydration material.     

Visualization of residual anisotropic interactions in crosslinked natural rubbers by dipolar local field measurements and H natural abundance NMR spectroscopy

An extension of the exploitation of indirect observation of ¹H nuclei through ¹³C resonances is presented in the case of crosslinked elastomers. It is demonstrated that, by using this method in vulcanized elastomers above T_g a direct visualization of residual dipolar interactions on different functional groups as well as their dependence on motional constraints is available. It is also shown that ²H natural abundance NMR spectra of elastomers provide similar information on motional constraints by way of residual quadrupolar interactions.     

The correlation of molecular orientation in liquid water by neutron and X-ray scattering

The neutron diffraction structure factor for heavy water at 22°c has been measured for momentum transfers, ?Q, up to a Q of 13 å ^-1. The results have been interpreted by abstracting the molecular structure effects as far as possible and using models for the correlation of orientation of pairs of molecules ranging from completely uncorrelated orientation to that for adjacent molecules in ice I. Neither these nor any of the popular models for the structure of water, nor a non-hydrogen bonded model, fit the neutron diffraction data over the whole range of Q. Nevertheless, information about the molecular-centres structure factor is obtained, especially for Q up to about 3 å ^-1.

The method of analysis is generalized and applied to x-ray diffraction data and in particular to x-ray data for liquid water. It is shown that this method of analysis has some advantages over the conventional one. The effect of correlation of molecular orientation is less than that of molecular structure on x-ray scattering by water and rather more extensive information is obtained for the molecular-centres structure factor than from neutron data—if the conventional assumption of atomic electron clouds is accepted.

A comparison of the x-ray and neutron scattering data for liquid heavy water shows that the two sets of data are reasonably consistent for any of the usual models for water, except for the region of Q between 3 and 5 å ^-1. The molecular-centres structure factor of water has a weak double humped first maximum with peaks at 2·0 å ^-1 and 2·9å ^-1, probably followed by a damped oscillation. This contrasts with atomic liquids but is similar to that found in liquid carbon tetrachloride. The structure of liquid water is not, therefore, necessarily unique or unusual.     

利用吸附有双硫腙的微昌萘萃取色层富集：———火焰原子吸收光 …

本文利用吸附有双硫脘的微昌萘作富集柱富集天然水中痕量铜，甲酰二甲胺洗脱，火焰原子吸收光谱法测定。对最佳吸附酸度，过柱流速，洗脱剂，共存离子干扰等进行了探讨。该方法的相对标准偏差为２．３％，加标回收率为９６％￣１０３％。通过对国家标准水样及实际天然水样的分析测定，结果令人满意。     

Measurements of neutron interference and polarization effects caused by nuclear and magnetic interaction

The effects of simultaneous phase shift and spin rotation on neutron waves were measured with the perfect crystal neutron interferometer. Using an unpolarized beam of slow neutrons characteristic “beat” effects of the interference pattern and a polarization of the neutrons behind the interferometer could be observed.