Parametric modeling of steady-state gradient coil vibration: Resonance dynamics under variations in cylinder geometry

Gradient coil (GC) vibration is the root cause of many problems in MRI adversely affecting scanner performance, image quality, and acoustic noise levels. A critical issue is that GC vibration will be significantly increased close to any GC mechanical resonances. It is well known that altering the dimensions of a GC fundamentally affects the mechanical resonances excited by the GC windings. The precise nature of the effects (i.e., how the resonances are affected) is however not well understood. The purpose of the present paper is to study how the mechanical resonances excited by closed whole-body Z-gradient coils are affected by variations in cylinder geometry. A mathematical Z-gradient coil vibration model recently developed and validated by the authors is used to theoretically study the resonance dynamics under variation(s) in cylinder: (i) length, (ii) mean radius, and (iii) radial thickness. The forced-vibration response to Lorentz-force excitation is in each case analyzed in terms of the frequency response of the GC cylinder's displacement. In cases (i) and (ii), the qualitative dynamics are simple: reducing the cylinder length and/or mean radius causes all mechanical resonances to shift to higher frequencies. In case (iii), the qualitative dynamics are much more complicated with different resonances shifting in different directions and additional dependencies on the cylinder length. The more detailed dynamics are intricate owing to the fact that resonances shift at comparatively different rates and this leads to several novel and theoretically interesting predicted effects. Knowledge of these effects advance our understanding of the basic mechanics of GC vibration and offer practically useful insights into how such vibration may be passively reduced.     

Microfluidic three-dimensional biomimetic tumor model for studying breast cancer cell migration and invasion in the presence of interstitial flow

Cell migration and invasion are critical steps in cancer metastasis, which are the major cause of death in cancer patients. Tumor-associated macrophages(TAMs) and interstitial flow(IF) are two important biochemical and biomechanical cues in tumor microenvironment, play essential roles in tumor progression. However, their combined effects on tumor cell migration and invasion as well as molecular mechanism remains largely unknown. In this work, we developed a microfluidic-based 3 D breast cancer model by co-culturing tumor aggregates, macrophages, monocytes and endothelial cells within 3 D extracellular matrix in the presence of IF to study tumor cell migration and invasion. On the established platform, we can precisely control the parameters related to tumor microenvironment and observe cellular responses and interactions in real-time. When co-culture of U937 with human umbilical vein endothelial cells(HUVECs) or MDA-MB-231 cells and tri-culture of U937 with HUVECs and MDA-MB-231 cells, we found that mesenchymal-like MDA-MB-231 aggregates activated the monocytes to TAM-like phenotype macrophages. MDA-MB-231 cells and IF simultaneously enhanced the macrophages activation by the stimulation of colony-stimulating factor 1(CSF-1). The activated macrophages and IF further promoted vascular sprouting via vascular endothelial growth factor(VEGFα) signal and tumor cell invasion. This is the first attempt to study the interaction between macrophages and breast cancer cells under IF condition. Taken together, our results provide a new insight to reveal the important physiological and pathological processes of macrophages-tumor communication. Moreover, our established platform with a more mimetic 3 D breast cancer model has the potential for drug screening with more accurate results.     

C-methyl flavonoid from the leaves of Cleistocalyx conspersipunctatus: α-glucosidase inhibitory,molecular docking simulation and biosynthetic pathway

We extracted one new C-methyl flavonoid, farrerol 7-O-β-d-(6-O-galloyl)glucopyranoside (1), along with 11 known flavonoids, from the Cleistocalyx (C.) conspersipunctatus leaves. Elucidation of these flavonoid structures was accomplished through spectroscopic investigation and electronic circular dichroism (ECD) computation. Compared to corosolic acid (IC₅₀: 15.5 ± 0.9 μM), an established inhibitor, the compound 1 (IC₅₀: 6.9 ± 1.2 μM) was found more active in suppressing α-glucosidase. These findings imply the potential of compound 1 as a valid α-glucosidase inhibitor, which also offer evidence for future animal experiments and clinical trials. Besides, molecular docking was employed to explore the probable mechanism for α-glucosidase–compound 1 interaction. The biosynthetic pathway of these flavonoids in C. conspersipunctatus were proposed.     

A comprehensive comparison between shortest-path HARP refinement,SinMod, and DENSEanalysis processing tools applied to CSPAMM and DENSE images

We addressed comprehensively the performance of Shortest-Path HARP Refinement (SP-HR), SinMod, and DENSEanalysis using 2D slices of synthetic CSPAMM and DENSE images with realistic contrasts obtained from 3D phantoms. The three motion estimation techniques were interrogated under ideal and no-ideal conditions (with MR induced artifacts, noise, and through-plane motion), considering several resolutions and noise levels. Under noisy conditions, and for isotropic pixel sizes of 1.5 mm and 3.0 mm in CSPAMM and DENSE images respectively, the nRMSE obtained for the circumferential and radial strain components were 10.7 ± 10.8% and 25.5 ± 14.8% using SP-HR, 11.9 ± 2.5% and 29.3 ± 6.5% using SinMod, and 6.4 ± 2.0% and 18.2 ± 4.6% using DENSEanalysis. Overall, the results showed that SP-HR tends to fail for large tissue motions, whereas SinMod and DENSEanalysis gave accurate displacement and strain field estimations, being the last which performed the best.     

Fabrication of multisegmented magnetic wires with micron-length copper spacers

Segmented magnetic nanowires have a distinctive magnetic signature which can be exploited in magnetic biosensors. We report on the fabrication of magnetic segmented nanowires with copper spacers a few microns long. The key to avoid dissolution of the magnetic segment by an electroless reaction with the Cu bath is to include an interlayer, which protects the magnetic segments from dissolution with concentrated Cu^2 + electrolytes. Ni alloyed with Co makes it magnetically soft and for a Co₈₀Ni₂₀ composition, the specific magnetization is reduced by only 15%, compared to pure Co.     

Total chromatic number of graphs with small genus

Given a graph G, a total k-coloring of G is a simultaneous coloring of the vertices and edges of G with k colors. Denote χ_ve (G) the total chromatic number of G, and c(Σ) the Euler characteristic of a surfase Σ. In this paper, we prove that for any simple graph G which can be embedded in a surface Σ with Euler characteristic c(Σ), χ_ve (G) = Δ (G) + 1 if c(Σ) > 0 and Δ (G) ≥ 13, or, if c(Σ) = 0 and Δ (G) ≥ 14. This result generalizes results in [3], [4], [5] by Borodin.     

A convenient synthesis of 3-methyleneoxindoles: cytotoxic metabolites of indole-3-acetic acids

3-Methyleneoxindole is a cytotoxic metabolite of indole-3-acetic acid with potential for use in cancer therapy. This species and ring-substituted analogues are conveniently synthesised from the corresponding isatins via a Peterson olefination.     

The metabolites and biotransformation pathways in vivo after oral administration of ocotillol,RT5, and PF11

Ocotillol, pseudo-ginsenoside RT5 (RT₅), and pseudo-ginsenoside F₁₁ (PF₁₁) are ocotillol-type saponins that have the same aglycone structure but with different numbers of glucose at the C-6 position. In this study, the metabolites of ocotillol, RT₅, and PF₁₁ in rat plasma, stomach, intestine, urine, and feces after oral administration were investigated by ultra-performance liquid chromatography coupled with time-of-flight mass spectrometry. The results showed that RT₅ was easily biotransformed into metabolites in vivo, whereas PF₁₁ and RT₅ were difficult to be biotransformed. Hydrogenation, dehydrogenation, dehydration, deglycosylation, deoxygenation, hydration, phosphorylation, deoxidation, glucuronidation, and reactions combining amino acid were speculated to be involved in the biotransformation of ocotillol, RT₅, and PF₁₁. Based on the structural analysis of metabolites, it was deduced that hydrogenation, dehydration, deoxidation, and reactions combining amino acid occurred on the aglycone structure, whereas deglycosylation, hydration, and phosphorylation occurred on the glycosyl chain. Further, metabolites in plasma, urine, feces, and tissues were different: First, glucuronidation products were found in urine, stomach, intestine, and feces, but not in plasma. Second, the ocotillol prototype was not identified in urine samples. Third, the RT₅ prototype was found in stomach, intestine, feces, and urine, but not in plasma.