Magnetic resonance imaging of mouse Ehrlich carcinoma growth inhibition by thiacarpine, an analogue of cytotoxic marine alkaloid polycarpine

The anticancer effect of thiacarpine, a synthetic analogue of the known cytotoxic alkaloid polycarpine isolated from the Pacific ascidian Polycarpa aurata, was investigated in vivo in experiments using mouse solid Ehrlich carcinoma tumor as the target. A high-resolution magnetic resonance imaging (MRI) technique using a MR tomograph "PharmaScan" US70/16 (Bruker, Ettlingen, Germany) was used for visualization and quantification of tumor size. Fluorescence microscopy and image analysis were applied to determine Ehrlich carcinoma cell chromatin condensing (apoptosis) and necrosis in Ehrlich carcinoma cells at the action of thiacarpine in in vitro experiments. The scan and size calculations of the tumor and some mouse organs were carried out during the experiments. Thiacarpine in a total dose of 100 mg/kg was found to exhibit the delay in growth of the mouse tumor. The antineoplastic effect of this compound was accompanied by an increase in the lifetime of experimental mice in comparison with the control group of animals. Our data show that the ability of thiacarpine to induce apoptosis in carcinoma cells may contribute to thiacarpine anticancer effects against mice solid Ehrlich carcinoma in vivo detected by MRI.     

Phase correction-based singularity function analysis for partial k-space reconstruction

Partial k-space acquisition is a conventional method in magnetic resonance imaging (MRI) for reducing imaging time while maintaining image quality. In this field, image reconstruction from partial k-space is a key issue. This paper proposes an approach fundamentally different from traditional techniques for reconstructing magnetic resonance (MR) images from partial k-space. It uses a so-called singularity function analysis (SFA) model based on phase correction. With such a reconstruction approach, some nonacquired negative spatial frequencies are first recovered by means of phase correction and Hermitian symmetry property, and then the other nonacquired negative and/or positive spatial frequencies are estimated using the mathematical SFA model. The method is particularly suitable for asymmetrical partial k-space acquisition owing to its ability of overcoming reconstruction limitations due to k-space truncations. The performance of this approach is evaluated using both simulated and real MR brain images, and compared with existing techniques. The results demonstrate that the proposed SFA based on phase correction achieves higher image quality than the initial SFA or the projection-onto-convex sets (POCS) method.     

In vivo determination of the time and location of mucoadhesive drug delivery systems disintegration in the gastrointestinal tract

OBJECTIVE: The objective of this study was to use magnetic resonance imaging (MRI) to detect the time when and the location at which orally delivered mucoadhesive drugs are released. MATERIALS AND METHODS: Drug delivery systems comprising tablets or capsules containing a mucoadhesive polymer were designed to deliver the polymer to the intestine in dry powder form. Dry Gd-DTPA [diethylenetriaminepentaacetic acid gadolinium(III) dihydrogen salt hydrate] powder was added to the mucoadhesive polymer, resulting in a susceptibility artifact that allows tracking of the application forms before their disintegration and that gives a strong positive signal on disintegration. Experiments were performed with rats using T(1)-weighted spin-echo imaging on a standard 1.5-T MRI system. RESULTS: The susceptibility artifact produced by the dry Gd-DTPA powder in tablets or capsules was clearly visible within the stomach of the rats and could be followed during movement towards the intestine. Upon disintegration, a strong positive signal was unambiguously observed. The time between ingestion and observation of a positive signal was significantly different for different application forms. Quantification of the remaining mucoadhesive polymer in the intestine 3 h after observed release showed significant differences in mucoadhesive effectiveness. CONCLUSION: MRI allows detection of the exact time of release of the mucoadhesive polymer in vivo, which is a prerequisite for a reliable quantitative comparison between different application forms.     

Comparison of tumor histology to dynamic contrast enhanced magnetic resonance imaging-based physiological estimates

Purpose

The purpose of this study was to compare histologically determined cellularity and extracellular space to dynamic contrast-enhanced magnetic resonance imaging (DCE MRI)-based maps of a two-compartment model's parameters describing tumor contrast agent extravasation, specifically tumor extravascular extracellular space (EES) volume fraction (v_e), tumor plasma volume fraction (v_p) and volume-normalized contrast agent transfer rate between tumor plasma and interstitium (K_TRANS/V_T).

Materials and Methods

Obtained v_e, v_p and K_TRANS/V_T maps were estimated from gadolinium diethylenetriamine penta-acetic acid DCE T₁-weighted gradient-echo images at resolutions of 469, 938 and 2500 μm. These parameter maps were compared at each resolution to histologically determined tumor type, and the high-resolution 469-μm maps were compared with automated cell counting using Otsu's method and a color-thresholding method for estimated intracellular (V_{intracellular}) and extracellular (V_{extracellular}) space fractions.

Results

The top five K_TRANS/V_T values obtained from each tumor at 469 and 938 μm resolutions are significantly different from those obtained at 2500 μm (P<.0001) and from one another (P=.0014). Using these top five K_TRANS/V_T values and the corresponding tumor EES volume fractions v_e, we can statistically differentiate invasive ductal carcinomas from noninvasive papillary carcinomas for the 469- and 938-μm resolutions (P=.0017 and P=.0047, respectively), but not for the 2500-μm resolution (P=.9008). The color-thresholding method demonstrated that v_e measured by DCE MRI is statistically similar to histologically determined EES. The V_{extracellular} obtained from the color-thresholding method was statistically similar to the v_e measured with DCE MRI for the top 10 K_TRANS/V_T values (P>.05). DCE MRI-based K_TRANS/V_T estimates are not statistically correlated with histologically determined cellularity.

Conclusion

DCE MRI estimates of tumor physiology are a limited representation of tumor histological features. Extracellular spaces measured by both DCE MRI and microscopic analysis are statistically similar. Tumor typing by DCE MRI is spatial resolution dependent, as lower resolutions average out contributions to voxel-based estimates of K_TRANS/V_T. Thus, an appropriate resolution window is essential for DCE MRI tumor diagnosis. Within this resolution window, the top K_TRANS/V_T values with corresponding v_e are diagnostic for the tumor types analyzed in this study.     

Influence of steady background gradients on the accuracy of molecular diffusion anisotropy measurements

Spatial susceptibility variations of body components lead to local gradients of the static magnetic field. Effects of such background gradients on fractional diffusion anisotropy (FA) measurements on whole-body magnetic resonance units operating at 1.5, 3.0 and 7.0 T were analyzed theoretically and experimentally. Analytical expressions were derived for the cases of diffusion occurring in isotropic media and in tissues with cylindrical symmetry (e.g., white matter tracts or skeletal musculature). Typical magnitudes of background gradient strengths were estimated from in vivo and in vitro measurements with B0 field mapping sequences. Additionally, numerical simulations of magnetic field distributions and resulting field gradients were performed considering tissue-air interfaces in simplified geometrical arrangements. For media with isotropic diffusion, both measurements and analytical calculations showed increasing FA inaccuracy with stronger coupling between diffusion-encoding and background gradients. For cylindrical symmetry, FA values were estimated for a standard diffusion tensor imaging protocol in a realistic scenario. At 1 mm distance from a water-air interface, susceptibility-related background gradients amount to approximately 9 mT/m at 7 T and lead to a relative error of the measured FA of up to 48%. The error in the anisotropy assessment rises considerably with increasing field strength and must be taken into account especially for experimental and clinical studies on modern high-field systems.     

Coherent X‐ray diffractive imaging of protein crystals

The technique of coherent X‐ray diffraction imaging (CXDI) has recently shown great promise for the study of inorganic nanocrystals. In this work the CXDI method has been applied to the study of micrometer‐size protein crystals. Finely sampled diffraction patterns of single crystals were measured and iterative phase‐retrieval algorithms were used to reconstruct the two‐dimensional shape of the crystal. The density maps have limited reproducibility because of radiation damage, but show clear evidence for crystal facets. Qualitative analysis of a number of single‐crystal diffraction peaks indicates the presence of inward surface contraction on 2 µm size crystals. A survey of several hundred diffraction patterns yielded a number of examples with dramatic single‐sided streaks, for which a plausible model is constructed.     

Monitoring membrane rafts in colorectal cancer cells by means of correlative fluorescence electron microscopy (CFEM)

Detergent-resistant membrane (DRM) rafts have been shown to play a pivotal role in regulating key cell biological processes, such as signal transduction, cellular transport and cell survival. The fine structure of membrane rafts are studied using various different imaging approaches and the outcomes are largely dependent on the detection methodology applied. All these microscopy techniques which employ light-, laser- and photon-optics, electrons as well as atomic force probing are characterized on their turn by their strengths and limitations for membrane raft identification. This explains in part the diversity of definitions available to describe these peculiar membrane structures. We present herewith an alternative and uncomplicated microscopy tool to study fluorescently labelled DRMs with information at the transmission electron microscopical level of the same cell, enabling us to obtain a snapshot of the morpho-functional relationships between the cell's interior and DRMs. The proposed approach of correlative fluorescence electron microscopy (CFEM) can therefore be considered as an additional alternative imaging approach to unravel DRM structure–function relationships from micro- to nanometre length scales, from the cell to the molecule.     

直接解调方法在嫦娥一号卫星X射线谱仪地面验证实验数据分析中的应用

"嫦娥一号"卫星是我国的第一颗月球探测卫星,运行轨道高度为200 km,预计工作寿命为一年,其上配备的X射线成像谱仪具备了对月表进行X射线探测、成像和对太阳X射线进行监测的功能.该X射线谱仪由两个全同的探测器阵列组成,其中,为了实现对月表主要化学元素分布及其含量进行探测的科学目标,在每个探测器阵列还配备了2个低能探测器单元.这4路低能探测器单元的面积为25 mm2,采用的都是厚度为500 μm,具有优良探测性能的Si-PIN探测器,其探测能区为1～10 keV,能量分辨率为～5%@5.9 kev.文章主要介绍了嫦娥一号卫星X射线谱仪的地面验证实验,并且根据X射线谱仪的能量响应矩阵,利用直接解调方法和基本参数法对X射线谱仪地面验证实验中的探测数据,特别是对盲测样品中的Mg,Al,Si等元素进行了定性和定量分析.     

一种开放式磁共振成像主磁体的设计方法

本文提出了一种开放式磁共振成像(MRI)超导磁体的设计方法.在对磁体模型进行简化的基础上获得初始的电流分布,然后将线圈截面的优化问题转化成一个非线性最小二乘问题,通过求解最小二乘问题得到实际的线圈截面参数.文章最后给出了一个设计算例.     

用云母弯晶谱仪探测Z箍缩等离子体X射线光谱

 为了研究Z箍缩等离子体辐射的X射线光谱,研制了可用于“阳”加速器上探测宽频谱范围的X射线椭圆弯曲晶体谱仪。该谱仪晶体分析器采用云母材料,椭圆焦距为1 350 mm,离心率为0.948 5,覆盖布拉格范围为30°~60°,可探测X射线波长范围为0.10~1.73 nm(0.86~1.00 nm除外),用X射线胶片接收光谱信号。探测实验在中国工程物理研究院“阳”加速器上进行,实验结果表明:谱仪获取了氩的类氢共振线L_ya及其伴线、类氦共振线(1s2p¹P₁-1s2¹S₀)w线及磁四级M₂2跃迁(1s2p³P₂-1s²¹S₀)x线、互组合跃迁(1s2p³P₁-1s²¹S­₀)y线、禁戒谱线(1s2p³S₁-1s²¹S₀)z线和K­_-a线,谱线分辨率达到564。实验证明弯晶谱仪适合于Z箍缩等离子体X射线光谱学诊断。