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Long- and short-range structure studies of KBT-KBZ solid-solutions using synchrotron radiation
The relaxor ferroelectric K0.5Bi0.5TiO3 has been synthesised in a solid-solution series with K0.5Bi0.5ZrO3, as K0.5Bi0.5Ti1−xZrxO3. High-resolution synchrotron X-ray powder diffraction and X-ray absorption near edge structure spectroscopy were used to characterise the long-range average and local structural behaviour. Rietveld refinements against diffraction data show that a pseudocubic tetragonal region exists across the whole solid-solution series, with truly cubic symmetry only observed at x = 1 (pure KBZ). Variable-temperature diffraction data for x = 0 (pure KBT) showed a broad ferroelectric transition from tetragonal to cubic symmetry at approximately 683 K with a coexistence of both phases close to that temperature, accompanied by a marked volume contraction. Ti K-edge data showed that Zr doping has a minimal effect on Ti off-centering, and revealed no evidence for local clustering. Metal L-edges showed that Ti4+ cations remain off-centered with increasing Zr content, while Zr4+ cations approach a higher-symmetry coordination environment, most likely due to the increased size of the Zr atoms. Although there is a minimal effect on actual Ti-offsets, an effective dilution of these environments by Zr doping leads to a reduction in polar domains and a diminished ferroelectric response. © 2015 Royal Society of Chemistr
Soft chemical synthesis and structural characterization of Y2HfxTi2−xO7
A novel soft chemistry route was developed to synthesize Y2HfxTi2−xO7 (0≤x≤2.0) oxide solid solution. An aqueous solution containing reactants was produced to ensure the combustion reaction taking place at the molecular level. A suite of characterization techniques, including X-ray diffraction, Raman, transmission electron spectroscopy, as well as X-ray absorption near edge structure (XANES), is employed to investigate the structural and phase changes of the series. Both X-ray and electron diffraction patterns show that the Y2HfxTi2−xO7 system undergoes a clear composition-induced phase transition from ordered pyrochlore to disordered defect-fluorite at x~1.5. On the other hand, Raman and XANES spectra reveal a gradual evolution of the local structure with the substitution of Hf for Ti. © 2014 Elsevier Ltd and Techna Group S.r.l
Nanofiltration applications of tough MWNT buckypaper membranes containing biopolymers
The ability of biopolymers (bovine serum albumin, lysozyme, chitosan, gellan gum and DNA) to facilitate formation of aqueous dispersions of MWNTs was investigated using a combination of absorption spectrophotometry and optical microscopy. Subsequently, self-supporting carbon nanotube membranes, known as buckypapers (BPs), were prepared by vacuum filtration of the dispersions. Microanalytical data obtained from the BPs confirmed the retention of biopolymers within their structures. Tensile test measurements performed on the BPs showed that incorporation of the biopolymers resulted in significant improvements in mechanical properties, compared to analogous BPs containing MWNTs and the low molecular mass dispersant Triton X-100. For example, MWNT/CHT BPs (CHT=chitosan) exhibited values for tensile strength, ductility, Young's modulus and toughness of 28±2MPa, 5.3±2.7%, 0.9±0.3GPa and 1.7±0.3J g−1, respectively. Each of these values are significantly greater than those obtained for MWNT/Trix BPs, prepared using a low molecular weight dispersant (6±3MPa, 1.3±0.2%, 0.6±0.3GPa and 0.10±0.06J g−1, respectively). This significant improvement in mechanical properties is attributed to the ability of the long biopolymer molecules to act as flexible bridges between the short CNTs. All BPs possessed hydrophilic surfaces, with contact angles ranging from 29±2° to 57±5°. Nitrogen gas porosimetry showed that the BPs have highly porous internal structures, while scanning electron microscopy (SEM) showed their surface morphologies have numerous pore openings. The permeability of the BPs towards water, inorganic salts, and dissolved trace organic contaminants (TrOCs), such as pharmaceuticals, personal care products, and pesticides, was investigated through filtration experiments. Of the twelve TrOCs investigated in this study, nine were rejected by more than 95% by BPs composed of MWNTs and chitosan. The latter BPs also demonstrated good rejection of both NaCl (30–55%) and MgSO4 (40–70%). © 2017 Elsevier B.V
Effects of ionizing radiation on mitochondria
The current concept of radiobiology posits that damage to the DNA in the cell nucleus is the primary cause for the detrimental effects of radiation. However, emerging experimental evidence suggests that this theoretical framework is insufficient for describing extranuclear radiation effects, particularly the response of the mitochondria, an important site of extranuclear, coding DNA. Here, we discuss experimental observations of the effects of ionizing radiation on the mitochondria at (1) the DNA and (2) functional levels. The roles of mitochondria in (3) oxidative stress and (4) late radiation effects are discussed. In this review, we summarize the current understanding of targets for ionizing radiation outside the cell nucleus. Available experimental data suggest that an increase in the tumoricidal efficacy of radiation therapy might be achievable by targeting mitochondria. Likewise, more specific protection of mitochondria and its coding DNA should reduce damage to healthy cells exposed to ionizing radiation. © 2013 Elsevier Inc
Can structural or functional changes following traumatic brain injury in the rat predict epileptic outcome?
Posttraumatic epilepsy (PTE) occurs in a proportion of traumatic brain injury (TBI) cases, significantly compounding the disability, and risk of injury and death for sufferers. To date, predictive biomarkers for PTE have not been identified. This study used the lateral fluid percussion injury (LFPI) rat model of TBI to investigate whether structural, functional, and behavioral changes post‐TBI relate to the later development of PTE. © 2013 International League Against Epileps
Triamidetriamine bearing macrobicyclic and macrotricyclic ligands: potential applications in the development of copper-64 radiopharmaceuticals
A versatile and straightforward synthetic approach is described for the preparation of triamide bearing analogues of sarcophagine hexaazamacrobicyclic cage ligands without the need for a templating metal ion. Reaction of 1,1,1-tris(aminoethyl)ethane (tame) with 3 equiv of 2-chloroacetyl chloride, yields the tris(α-chloroamide) synthetic intermediate 6, which when treated with either 1,1,1-tris(aminoethyl)ethane or 1,4,7-triazacyclononane furnished two novel triamidetriamine cryptand ligands (7 and 8 respectively). The Co(III) and Cu(II) complexes of cryptand 7 were prepared; however, cryptand 8 could not be metalated. The cryptands and the Co(III) complex 9 have been characterized by elemental analysis, 1H and 13C NMR spectroscopy, and X-ray crystallography. These studies confirm that the Co(III) complex 9 adopts an octahedral geometry with three facial deprotonated amido-donors and three facial amine donor groups. The Cu(II) complex 10 was characterized by elemental analysis, single crystal X-ray crystallography, cyclic voltammetry, and UV–visible absorption spectroscopy. In contrast to the Co(III) complex (9), the Cu(II) center adopts a square planar coordination geometry, with two amine and two deprotonated amido donor groups. Compound 10 exhibited a quasi-reversible, one-electron oxidation, which is assigned to the Cu2+/3+ redox couple. These cryptands represent interesting ligands for radiopharmaceutical applications, and 7 has been labeled with 64Cu to give 64Cu-10. This complex showed good stability when subjected to l-cysteine challenge whereas low levels of decomplexation were evident in the presence of l-histidine. © 2013 American Chemical Societ
Effect of non-ionic surfactants and its role in K intercalation in electrolytic manganese dioxide
The effect of non-ionic surface active agents (surfactants) Triton X-100 (TX-100) and Tween-20 (Tw-20) and their role in potassium intercalation in electrolytic manganese dioxide (EMD) produced from manganese cake has been investigated. Electrosynthesis of MnO2 in the absence or presence of surfactant was carried out from acidic MnSO4 solution obtained from manganese cake under optimized conditions. A range of characterization techniques, including field emission scanning electron microscopy, transmission electron microscopy (TEM), Rutherford back scattering (RBS), and BET surface area/porosity studies, was carried out to determine the structural and chemical characteristics of the EMD. Galvanostatic (discharge) and potentiostatic (cyclic voltammetric) studies were employed to evaluate the suitability of EMD in combination with KOH electrolyte for alkaline battery applications. The presence of surfactant played an important role in modifying the physicochemical properties of the EMD by increasing the surface area of the material and hence, enhancing its electrochemical performance. The TEM and RBS analyses of the discharged EMD (γ-MnO2) material showed clear evidence of potassium intercalation or at least the formation of a film on the MnO2 surface. The extent of intercalation was greater for EMD deposited in the presence of TX-100. Discharged MnO2 showed products of Mn2+ intermediates such as MnOOH and Mn3O4. © 2014 ASM International (ASM) and The Minerals, Metals & Materials Society (TMS
Positron annihilation lifetime study of radiation-damaged natural zircons
Zircons are a well-known candidate waste form for actinides and their radiation damage behaviour has been widely studied by a range of techniques. In this study, well-characterised natural single crystal zircons have been studied using Positron Annihilation Lifetime Spectroscopy (PALS). In some, but not all, of the crystals that had incurred at least half of the alpha-event damage of ∼1019 α/g required to render them structurally amorphous, PALS spectra displayed long lifetimes corresponding to voids of ∼0.5 nm in diameter. The long lifetimes corresponded to expectations from published Small-Angle X-ray Scattering data on similar samples. However, the non-observation by PALS of such voids in some of the heavily damaged samples may reflect large size variations among the voids such that no singular size can be distinguished or. Characterisation of a range of samples was also performed using scanning electron microscopy, optical absorption spectroscopy, Raman scattering and X-ray scattering/diffraction, with the degree of alpha damage being inferred mainly from the Raman technique and X-ray diffraction. The observed void diameters and intensities of the long lifetime components were changed somewhat by annealing at 700 °C; annealing at 1200 °C removed the voids entirely. The voids themselves may derive from He gas bubbles or voids created by the inclusion of small quantities of organic and hydrous matter, notwithstanding the observation that no voidage was evidenced by PALS in two samples containing hydrous and organic matter. © 2016 Elsevier B.V
Positron emission tomography and functional characterization of a complete PBR/TSPO knockout
The evolutionarily conserved peripheral benzodiazepine receptor (PBR), or 18-kDa translocator protein (TSPO), is thought to be essential for cholesterol transport and steroidogenesis, and thus life. TSPO has been proposed as a biomarker of neuroinflammation and a new drug target in neurological diseases ranging from Alzheimer’s disease to anxiety. Here we show that global C57BL/6-Tspotm1GuWu(GuwiyangWurra)-knockout mice are viable with normal growth, lifespan, cholesterol transport, blood pregnenolone concentration, protoporphyrin IX metabolism, fertility and behaviour. However, while the activation of microglia after neuronal injury appears to be unimpaired, microglia from GuwiyangWurraTSPO knockouts produce significantly less ATP, suggesting reduced metabolic activity. Using the isoquinoline PK11195, the ligand originally used for the pharmacological and structural characterization of the PBR/TSPO, and the imidazopyridines CLINDE and PBR111, we demonstrate the utility of GuwiyangWurraTSPO knockouts to provide robust data on drug specificity and selectivity, both in vitro and in vivo, as well as the mechanism of action of putative TSPO-targeting drugs. Copyright © 2014, Springer Natur
4D PET iterative deconvolution with spatiotemporal regularization for quantitative dynamic PET imaging
Quantitative measurements in dynamic PET imaging are usually limited by the poor counting statistics particularly in short dynamic frames and by the low spatial resolution of the detection system, resulting in partial volume effects (PVEs). In this work, we present a fast and easy to implement method for the restoration of dynamic PET images that have suffered from both PVE and noise degradation. It is based on a weighted least squares iterative deconvolution approach of the dynamic PET image with spatial and temporal regularization. Using simulated dynamic [11C] Raclopride PET data with controlled biological variations in the striata between scans, we showed that the restoration method provides images which exhibit less noise and better contrast between emitting structures than the original images. In addition, the method is able to recover the true time activity curve in the striata region with an error below 3% while it was underestimated by more than 20% without correction. As a result, the method improves the accuracy and reduces the variability of the kinetic parameter estimates calculated from the corrected images. More importantly it increases the accuracy (from less than 66% to more than 95%) of measured biological variations as well as their statistical detectivity. © 2015 Elsevier Inc