Characteristics and efficacy of fish-derived gelatin microparticles as an embolic agent in a rabbit renal model: regulation of the degradation period by molecular weight

PURPOSE:To evaluate the embolic effect of fish-derived gelatin microparticles (GMPs) and compare the degradation periods and biocompatibilities of different molecular weight (MW) GMPs in a rabbit model.METHODS:GMPs were designed to degrade within 21 days (high MW GMP, 15-30 kDa) and 2 days (low MW GMP, 5-15 kDa) in vivo. Renal arteries of 24 rabbits were embolized using both high and low MW GMPs (155-350 µm). Rabbits were sacrificed either immediately after embolization, or after follow-up (F/U) angiogram on days 2 and 21 of embolization, respectively (4 rabbits in each of the 6 subgroups). Pathological changes of recanalized vessels were evaluated using the Banff classification. For the in vitro study, each type of GMP was mixed with normal saline and morphological changes were compared for 14 days.RESULTS:Fish-derived GMPs showed effective embolization. On 2-day F/U angiography, occluded vessels were more recanalized to the peripheral branches in low MW group. On day 21, a parenchymal perfusion defect recovered to a greater extent in low MW group than that in high MW group. Mean Banff scores for intimal arteritis on 2-day F/U and interstitial fibrosis on 21-day F/U were higher in high MW group (1.75 ± 0.58 vs. 0.19 ± 0.4 and 2.56 ± 0.63 vs. 0.88 ± 0.89; P < .001). On in vitro assessment, low MW GMP lost the spherical shape and degraded, and was invisible on microscopy on day 6, whereas high MW GMP was only partially degraded after 2 weeks.CONCLUSION:Fish-derived GMPs showed effective embolization in a rabbit model. Low MW GMPs degraded within 2 days with a low inflammatory response

Transparent, low resistance, and flexible amorphous ZnO-doped In2O3 Anode Grown on a PES Substrate

Transparent and low resistance amorphous ZnO-doped In2O3 (IZO) anode films were grown by radio-frequency (rf) sputtering on an organic passivated polyethersulfone (PES) substrate for use in flexible organic light-emitting diodes (OLEDs). Under optimized growth conditions, a sheet resistance of 15.2 /, average transmittance above 89% in the green range, and a root mean square roughness of 0.375 nm were obtained, even for the IZO anode film grown in a pure Ar ambient without the addition of oxygen as a reactive gas. All of the IZO anode films had an amorphous structure regardless of the rf power and the working pressure due to the low substrate temperature of 50°C and the structural stability of the amorphous IZO films. In addition, an X-ray photoelectron spectroscopy depth profile obtained for the IZO/PES showed no obvious evidence of interfacial reactions between the IZO anode and the PES substrate, except for some indiffusion of oxygen atoms from the IZO anode. Furthermore, the current-voltage-luminance of the flexible OLEDs fabricated on IZO anode was found to be critically dependent on the sheet resistance of the IZO anode.This work was supported by a Korea Research Foundation grant funded by the Korean Government (MOEHRD: Basic Research Promotion Fund)(KRF-2006-003-D00243) and the Ministry of Commerce, Industry and Energy

Enhancement of hole injection using ozone treated Ag nanodots dispersed on indium tin oxide anode for organic light emitting diodes

The authors report the enhancement of hole injection using an indium tin oxide (ITO) anode covered with ultraviolet (UV) ozone-treated Ag nanodots for fac tris (2-phenylpyridine) iridium Ir(ppy)3-doped phosphorescent organic light-emitting diodes (OLEDs). X-ray photoelectron spectroscopy and UV-visible spectrometer analysis exhibit that UV-ozone treatment of the Ag nanodots dispersed on the ITO anode leads to formation of Ag2O nanodots with high work function and high transparency. Phosphorescent OLEDs fabricated on the Ag2O nanodot-dispersed ITO anode showed a lower turn-on voltage and higher luminescence than those of OLEDs prepared with a commercial ITO anode. It was thought that, as Ag nanodots changed to Ag2O nanodots by UV-ozone treatment, the decrease of the energy barrier height led to the enhancement of hole injection in the phosphorescent OLEDs.This work was supported by Korea Research Foundation grant funded by Korean Government (MOEHRD: Basic Research Promotion Fund)(KRF-2006-003-D00243) and Ministry of Commerce, Industry, and Energy

Transparent Conducting Indium Zinc Tin Oxide Anode for Highly Efficient Phosphorescent Organic Light Emitting Diodes

The preparation and characteristics of a transparent conducting indium zinc tin oxide (IZTO) anode for highly efficient phosphorescent organic light emitting diodes (OLEDs) is described. The resistivity and transmittance of the IZTO anode are comparable to reference In2O3 (ITO) anode films even though it was prepared at room temperature. In addition, the work function of the ozone-treated amorphous IZTO anode (5.12±0.02 eV) is much higher than that of ozone-treated reference ITO anodes (4.94±0.02 eV). The current-voltage-luminance characteristics and efficiencies of OLEDs prepared on the IZTO anode are critically dependent on the sheet resistance of the IZTO anode. Furthermore, both the quantum efficiency and power efficiency of the OLED fabricated on the amorphous IZTO anode are much higher than those of an OLED with the reference ITO anode due to the higher work function of the IZTO anode than those of conventional ITO anode. This indicates that IZTO is an alternative material for conventional ITO anodes used in OLEDs and flexible displays.This work was supported by a Korea Research Foundation Grant funded by the Korea Government MOEHRD: Basic Research Promotion Fund grant no. KRF-2006-331-D00243 and the Ministry of Commerce, Industry, and Energy

Dynamic relocalization of NHERF1 mediates chemotactic migration of ovarian cancer cells toward lysophosphatidic acid stimulation

NHERF1/EBP50 (Na+/H+ exchanger regulating factor 1; Ezrin-binding phosphoprotein of 50 kDa) organizes stable protein complexes beneath the apical membrane of polar epithelial cells. By contrast, in cancer cells without any fixed polarity, NHERF1 often localizes in the cytoplasm. The regulation of cytoplasmic NHERF1 and its role in cancer progression remain unclear. In this study, we found that, upon lysophosphatidic acid (LPA) stimulation, cytoplasmic NHERF1 rapidly translocated to the plasma membrane, and subsequently to cortical protrusion structures, of ovarian cancer cells. This movement depended on direct binding of NHERF1 to C-terminally phosphorylated ERM proteins (cpERMs). Moreover, NHERF1 depletion downregulated cpERMs and further impaired cpERM-dependent remodeling of the cell cortex, suggesting reciprocal regulation between these proteins. The LPA-induced protein complex was highly enriched in migratory pseudopodia, whose formation was impaired by overexpression of NHERF1 truncation mutants. Consistent with this, NHERF1 depletion in various types of cancer cells abolished chemotactic cell migration toward a LPA gradient. Taken together, our findings suggest that the high dynamics of cytosolic NHERF1 provide cancer cells with a means of controlling chemotactic migration. This capacity is likely to be essential for ovarian cancer progression in tumor microenvironments containing LPA

Effects of Titanium Mesh Surfaces-Coated with Hydroxyapatite/β-Tricalcium Phosphate Nanotubes on Acetabular Bone Defects in Rabbits

The management of severe acetabular bone defects in revision reconstructive orthopedic surgery is challenging. In this study, cyclic precalcification (CP) treatment was used on both nanotube-surface Ti-mesh and a bone graft substitute for the acetabular defect model, and its effects were assessed in vitro and in vivo. Nanotube-Ti mesh coated with hydroxyapatite/β-tricalcium phosphate (HA/β-TCP) was manufactured by an anodizing and a sintering method, respectively. An 8 mm diameter defect was created on each acetabulum of eight rabbits, then treated by grafting materials and covered by Ti meshes. At four and eight weeks, postoperatively, biopsies were performed for histomorphometric analyses. The newly-formed bone layers under cyclic precalcified anodized Ti (CP-AT) meshes were superior with regard to the mineralized area at both four and eight weeks, as compared with that under untreated Ti meshes. Active bone regeneration at 2–4 weeks was stronger than at 6–8 weeks, particularly with treated biphasic ceramic (p &lt; 0.05). CP improved the bioactivity of Ti meshes and biphasic grafting materials. Moreover, the precalcified nanotubular Ti meshes could enhance early contact bone formation on the mesh and, therefore, may reduce the collapse of Ti meshes into the defect, increasing the sufficiency of acetabular reconstruction. Finally, cyclic precalcification did not affect bone regeneration by biphasic grafting materials in vivo

Mechanisms of Toughness Improvement in Charpy Impact and Fracture Toughness Tests of Non-heat-treating Cold-drawn Steel Bar

In this study, toughness properties of a non-heat-treating cold-drawn bar were examined by Charpy impact test and fracture toughness test, and the toughness enhancement mechanisms were clarified in relation with microstructure. As the thickness of pearlite bands decreased after the cold drawing, the Charpy impact energy of the cold-drawn bar was higher than that of the as-rolled bar, which could be reasonably explained by the thin sheet toughening. On the other hand, thin pearlite bands negatively affected the fracture toughness because of the decreased spacing between crack or void initiation sites inside the fracture process zone in front of the pre-fatigued crack tip. The Charpy impact test data could also be correlated with the absorbed energy of the dynamic compressive test specimen whose orientation was matched with the hammer impact direction of the Charpy impact test, although the Charpy impact and dynamic compressive test specimens had a notched body and a smooth body, respectively. (C) 2013 Elsevier B.V. All rights reserved.X111412sciescopu

Thin and Flexible Solid Electrolyte Membranes with Ultrahigh Thermal Stability Derived from Solution-Processable Li Argyrodites for All-Solid-State Li-Ion Batteries

Sheet-type solid electrolyte (SE) membranes are essential for practical all-solid-state Li batteries (ASLBs). To date, SE membrane development has mostly been based on polymer electrolytes with or without the aid of liquid electrolytes, which offset thermal stability (or safety). In this study, a new scalable fabrication protocol for thin (40-70 mu m) and flexible single-ion conducting sulfide SE membranes with high conductance (29 mS) and excellent thermal stability (up to similar to 400 degrees C) is reported. Electrospun polyimide (PI) nonwovens provide a favorable porous structure and ultrahigh thermal stability, thus accommodating highly conductive infiltrating solution-processable Li6PS5Cl0.5Br0.5 (2.0 mS cm(-1)). LiNi0.6Co0.2Mn0.2O2/graphite ASLBs using 40 mu m thick Li6PS5Cl0.5Br0.5-infiltrated PI membranes show promising performances at 30 degrees C (146 mA h g(-1)) and excellent thermal stability (marginal degradation at 180 degrees C). Moreover, a new proof-of-concept fabrication protocol for ASLBs at scale that involves the injection of liquefied SEs into the electrode/PI/electrode assemblies is successfully demonstrated for LiCoO2/PI-Li6PS5Cl0.5Br0.5/Li4Ti5O12 ASLBs