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The goal of this study was to evaluate the diagnostic performance of 3D amide proton transfer-weighted (3D-APTW) imaging and 3D pseudocontinuous arterial spin labelling (3D-pCASL) alone and in combination in grading gliomas (low-grade glioma (LGG) vs. high-grade glioma (HGG)) and correlating isocitrate dehydrogenase (IDH) mutation status.Preoperatively, 81 patients with pathologically confirmed gliomas underwent 3.0-T magnetic resonance imaging (MRI) examinations. The APTW, relative APTW (rAPTW), cerebral blood flow (CBF), and relative CBF (rCBF) values were calculated to evaluate the solid components of the tumours. The MRI parameters were compared in the classification of gliomas by independent- and paired-samples t tests. A receiver operating characteristic (ROC) curve was constructed, and the area under the ROC curve (AUC) was calculated to assess the diagnostic performance of each parameter and the combination of the rAPTW and rCBF values.Patients with HGG showed significantly higher APTW, rAPTW, CBF, and rCBF values than those with LGG (all p 0.001). In the ROC curve analysis, the AUC of rAPTW was the highest at 0.90. By adding the rAPTW signal to the rCBF values, the diagnostic ability of the combined parameters improved from 0.90 to 0.96. The rAPTW value yielded the highest AUC (0.92) in correlating the IDH mutation status, and the diagnostic ability improved to 0.96 by adding it to the rCBF value.3D-APTW imaging combined with 3D-pCASL imaging may be used to aid assessment of grading glioma and IDH mutation status.

Stretchable conductive fibers offer unparalleled advantages in the development of wearable strain sensors for smart textiles due to their excellent flexibility and weaveability. However, the practical applications of these fibers in wearable devices are hindered by either contradictory properties of conductive fibers (high stretchability versus high sensing stability), or lack of manufacturing scalability. Herein, we present a facile approach for highly stretchable self-crimping fiber strain sensors based on a polyether-ester (TPEE) elastomer matrix using a side-by-side bicomponent melt-spinning process involving two parallel but attached components with different shrinkage properties. The TPEE component serves as a highly elastic mechanical support layer within the bicomponent fibers, while the conductive component (E-TPEE) of carbon black (CB), multiwalled carbon nanotubes (MCNTs) and TPEE works as a strain-sensitive layer. In addition to the intrinsic elasticity of the matrix, the TPEE/E-TPEE bicomponent fibers present an excellent form of elasticity due to self-crimping. The self-crimping elongation of the fibers can provide a large deformation, and after the crimp disappears, the intrinsic elastic deformation is responsible for monitoring the strain sensing. The reliable strain sensing range of the TPEE/E-TPEE composite fibers was 160%–270% and could be regulated by adjusting the crimp structure. More importantly, the TPEE/E-TPEE fibers had a diameter of 30–40 µm and tenacity of 40–50 MPa, showing the necessary practicality. This work introduces new possibilities for fiber strain sensors produced in standard industrial spinning machines.

Supercapacitors (SCs) are drawing considerable attention because of their remarkable power density, long cycling stability, quick charging/discharging, and environmentally friendly characteristics. They are currently applied in electronic devices and wearable energy storage systems. Recently, the use of asymmetric supercapacitors (ASCs) has been acknowledged as a valid strategy to improve energy density of SCs due to the combination of electric double-layered anodes and redox-schemed cathodes. Here, mesoporous hollow NiCo2S4 sub-microspheres and porous graphene/single-walled carbon nanotubes are synthesized by a simple and elegant method without any use of templates. The as-synthesized products exhibit improved capacitive performance and extraordinary stability. An assembled asymmetric supercapacitor with graphene/single-walled carbon nanotubes and NiCo2S4 as its negative and positive electrodes, respectively, delivers a maximum energy density of 45.3 W h kg−1 (at 800 W kg−1) and an outstanding cycling life (87.5% over 20,000 cycles). This suggests that the obtained products possess huge potential to become the next generation of electrode materials for future energy storage devices.

Cellulose/aromatic polysulfonamide (PSA) alloy fibers with good flame retardant properties were successfully prepared by changing the viscosity ratio of cellulose and PSA solutions. To reduce the content of PSA in the alloy fibers, cellulose and PSA with different molecular weight were adopted to prepare the alloy fibers. From the results of the limiting oxygen index(LOI) and the self-extinguishing time away from the flame, it was shown that the flame retardant properties of the alloy fibers were improved as the viscosity of PSA/[BMIM]Cl solution was lowered. The contact angle and the water retention values of the alloy fibers showed that the moisture absorption was strengthened with the addition of cellulose. To verify the properties of the alloy fiber, phase morphologies were characterized by laser scanning confocal microscope (LSCM). An analogous “sheath-core” structure in the cross section of the alloy fibers was shown when the viscosity of PSA/[BMIM]Cl solution was lower enough than that of cellulose/[BMIM]Cl solution. The lower viscosity PSA component was observed to migrate to the outer layer of the fiber, while the higher viscosity cellulose remained within the inner core of the fiber during the spinning process. This behavior improved the flame retardant properties of the alloy fibers at certain weight ratios. This work provides an effective way to prepare cellulose/PSA alloy fibers with improved flame retardancy, hygroscopic behavior, and mechanical strength by the regulating the phase morphology.

1-Butyl-3-methylimidazolium chloride ([BMIM]Cl) was selected as co-solvent to dissolve cellulose and silk fibroin and the cellulose/silk fibroin blend fibers were fabricated with dry-jet wet spinning technology. The phase morphology of cellulose and silk fibroin in the blend fibers was studied by scanning electron microcopy and laser scanning confocal microscope. It is shown that the cellulose is in the continuous phase and silk fibroin exists as “fibril-like” in cellulose, in which the radial dimension of silk fibroin phase is 0.5–1.0 μm. The phase size of silk fibroin along the fiber axis increased with the increase of silk fibroin content and draw ratio. From the wide-angle X-ray scattering, it is found that the total crystallinity of the blend fibers decreased with increasing silk fibroin content. The hydrogen bond between cellulose and silk fibroin was observed from Fourier transform infrared spectra. Although the tensile strength and initial modulus of blend fibers decreased with increasing silk fibroin content, the tensile strength of blend fibers contain 35 wt% silk fibroin was up to 191 MPa.

In order to verify the elastic response of copolyether-ester (PEE) fibers on their phase morphology and structure, the PEE fibers based on poly(butylene terephthalate) (PBT) as hard segments and poly(terramethylene glycol) (PTMG) as soft segments were prepared by melt spinning, the as-spun fibers were then heat-drawn and heat-set at different conditions. From the analysis of the mechanical properties, it is shown that the tenacity as well as elastic recovery of the fibers increased with the increasing heat-draw ratios, the elongation at break decreased. The morphological and structural were evaluated by small angle X-ray scattering (SAXS), wide angle X-ray scattering (WAXS) and birefringence. When the melt-spun PEE fibers were heat-drawn, higher crystallinity and orientation, larger size of lamellae structure was formed within the fibers, it is also much easier to form higher phase separation. This structure will contribute to better elastic performances of PEE fibers.

To analyze cardiac magnetic resonance imaging (CMR) characteristics in patients with isolated left ventricular noncompaction (IVNC) and assess its value in the diagnosis of IVNC in a Chinese adult Han population. We collected a consecutive series of 30 patients with IVNC from January 1, 2007, to December 31, 2008. During the same period, we prospectively included patients drawn from groups given a potential differential diagnosis for IVNC. All magnetic resonance images were analyzed using 17-segment model. Left ventricular ejection fraction was significantly lower for patients with DCM (16.2 ± 5.2%, P 0.001) and higher in AR (47.6 ± 16.2%, P = 0.009), AS (54.6 ± 21.1%, P = 0.001) and HHD (62.4 ± 6.8%, P 0.001) compared with IVNC (33.0 ± 14.1%). The two-layered structure was most frequently seen at the apical segments, followed by the mid-cavity and basal segments in patients with INVC. The anterior and lateral walls were more commonly involved in patients with IVNC. The number of noncompacted segments and end-diastolic ratio of non-compacted to compacted myocardium (NC/C ratio) was greater in patients with IVNC than in other five groups. The end-diastolic NC/C ratio of2.5 had 96.4% sensitivity and 97.4% specificity for identifying patients with IVNC. CMR provides an accurate and reliable evaluation of the localization and extent of noncompacted myocardium at end-diastole. The end-diastolic NC/C ratio of2.5 had high diagnostic accuracy for IVNC in a Chinese adult Han population.