Effects of Electrospinning Parameters on the Microstructure of PVP/TiO2 Nanofibers.

Titanium dioxide has excellent chemical, electrical, and optical properties, as well as good chemical stability. For that reason, it is widely used in many fields of study and industry, such as photocatalysts, organic solar cells, sensors, dental implants, and other applications. Many nanostructures of TiO2 have been reported, and electrospinning is an efficient practical technique that has a low cost and high efficiency. In various studies on improving performance, the researchers created nanofibers with suitable microstructures by changing various properties and the many process parameters that can be controlled. In this study, PVP/TiO2 nanofibers were fabricated by the electrospinning process. The diameters of the nanofibers were controlled by various parameters. To understand the effects on the diameter of the nanofibers, various process parameters were controlled: the molecular weight and concentration of the polymers, deionized water, applied voltage, fluid velocity, and concentration of titanium precursor. The average diameter of the PVP nanofibers was controlled in a range of 42.3 nm to 633.0 nm. The average diameter of the PVP/TiO2 nanofibers was also controlled in a range of 63.5 nm to 186.0 nm after heat treatment.

Upconversion properties in lanthanide doped layered-perovskite, CsBiNb2O7.

Despite advances of lanthanide-doped upconversion (UC) materials, the applications such as light-emitting diode and biological imaging are limited by low quantum efficiency. For this context, the understanding of unique interactions between the doped-lanthanides and the host crystals has attracted a huge amount of the researcher's interest. In particular, it was revealed that doping lanthanide ions in a non-centrosymmetric site of host lattice is the cause of relaxation of the Laporte selection rule in the 4f-4f transition of lanthanide ions. One of the layered perovskites CsBiNb2O7 is known to have non-centrosymmetric sites, which would lead to highly bright UC emission. Nevertheless, to our knowledge, there has been no research on the UC comparison between host materials of CsBiNb2O7 with other hosts. In this article, we present the UC intensity comparison of Yb3+-Er3+ ion doped CsBiNb2O7, NaYF4, BaTiO3, and SrTiO3 hosts (the UC in CsBiNb2O7:Er3+,Yb3+ was 2.4 times that of NaYF4:Er3+,Yb3+ and ∼70 times that of SrTiO3:Er3+,Yb3+). After that, we dig into UC, downshifting, and double beam system UC properties. The activator concentration was optimized by varying the doping ratio of Yb3+ and Er3+, and we found out the main reason for the concentration quenching behavior in Er3+ ion doped CsBiNb2O7 is dipole-dipole interaction. In addition, the double excitation experiment indicates that the absorption (4I15/2 → 4I13/2) factor is stronger than the stimulated emission (4I13/2 → 4I15/2) factor in CsBiNb2O7 under 1540 nm laser irradiation.

Photocatalytic Methylene Blue Degradation of Electrospun Ti-Zn Complex Oxide Nanofibers.

Photocatalysts are the most important technology in air pollution removal and the detoxification of organic materials. Doping and complexation are among the most used methods to improve the efficiency of photocatalysts. Titanium dioxide and zinc oxide nanomaterials are widely used materials for photocatalysts and the degradation of toxic materials. Their mixed structure can be fabricated by many methods and the structure affects their properties. Nanofibers are efficient materials for photocatalysts due to their vertically formed structure, which improves the charge separation of photoelectrons. We fabricated them by an electrospinning process. A precursor consisting of titanium 4-isopropoxide, zinc acetate dihydrate and polyvinylpyrrolidone was used as a spinning solution for a mixed structure of titanium dioxide and zinc oxide with different molar ratios. They were then calcined, crystallized by heat treatment and analyzed by thermogravimetric-differential thermal analysis (TG-DTA), X-ray diffractometer (XRD), field emission scanning electron microscope (FE-SEM) and energy-dispersive spectroscope (EDS). After annealing, the average diameters of the Ti-Zn complex oxide nanofibers were 237.6-278.6 nm with different salt ratios, and multiple crystalline structures were observed, namely TiO2, ZnO, ZnTiO3 and Zn2TiO4. We observed the photocatalytic performance of the samples and compared them according to the photodegradation of methylene blue. The methylene blue concentration decreased to 0.008-0.650 after three hours, compared to an initial concentration of 1, with different metal oxide structures.

Enhancing the organoleptic and functional properties of jujube by a quick aging process.

Black jujube was made by aging dried jujube and its physiochemical characteristics, antioxidant activities and α-glucosidase inhibitory activities were evaluated. The moisture and sugar contents were increased depending on the period of aging times and the pH was reduced thereby increasing acidity. The color of black jujube extract was changed from red to black resulting in decreases of Hunter color values L, a and b. As the aging progressed, sucrose was decomposed by increasing glucose and fructose, indicating higher contents of the total reducing sugars. Among the six different types of organic acids extracted from dried jujube, the levels of oxalic acid and citric acid were increased as the aging progressed. The total polyphenol contents in ethanol and water extracts of dried jujube were 7.74 and 8.12 mg/g, respectively. The water extract of black jujube aged for 48 hr contained the highest polyphenol contents at 16.82 mg/g. The 5'-hydroxymethylfurfural (5'-HMF) contents of black jujube extract significantly increased by longer aging times, and contained higher contents in the ethanol extract than water extract. The ethanol extract of black jujube showed the highest 5'-HMF content with 338.89 mg% after aging for 3 days. Also, IC50 values of black jujube aged for 72 hr evaluated by DPPH and ABTS radical assays were 0.54 and 0.59 mg/mL, respectively. α-Glucosidase inhibitory activities of black jujube at the concentration of 3.33 mg/mL (ethanol extract) increased from 65 to 80 % after aging for 72 hr.

Induction of apoptosis by immature fruits of Prunus salicina Lindl. cv. Soldam in MDA-MB-231 human breast cancer cells.

The goal of this study was to evaluate the anticancer effect of Prunus salicina Lindl. cv. Soldam at three maturity stages (immature, midmature and mature stages). Previous studies have shown that this fruit (plums) possesses hematopoiesis effects, prevents osteoporosis and has anti-mutagenic effects. An acetone extract of immature P. salicina Lindl. cv. Soldam fruit contained higher levels of total phenolics and condensed tannins than midmature and mature plums. The results showed that an acetone extract of immature plums possesses cytotoxic effects, which are related to the activity of the total polyphenols in the fruits. Apoptosis in MDA-MB-231 cells mediated by the immature plums was associated with an increase in Bax levels and a reduction in Bcl-2 levels and the cleavage of caspase 3, caspase 7, caspase 9 and poly-(ADP-ribose) polymerase. These results indicate that immature fruit of P . salicina Lindl. cv. Soldam can be regarded as a safe and promising new dietary source for decreasing the risk of developing breast cancer.

Metabolism of subtoxic level of selenite by double-perfused small intestine in rats.

Intestinal metabolism of the subtoxic level of selenite in rats was investigated using a double-perfusion system, which is an in situ, in vitro preparation in which the intestinal lumen and its vasculature are perfused simultaneously. The toxicity of sodium selenite was determined by inhibition of 3-O-methyl glucose (3MG) absorption and by histological examination. Levels of 1.2 mM selenite were required to significantly (p<0.05) reduce 3MG intestinal absorption (58+/-11%, mean+/-SD). Cation-exchange chromatography was used to determine the chemical forms of Se from selenite after using luminal concentrations of 1-200 microM in vascular perfusates. The chemical forms were selenite, selenodiglutathione (GS-Se-SG), mixed selenoglutathione plus cysteine (GS-Se-CYS), selenodicysteine (CYS-Se-CYS), protein-bound Se, and unidentified selenocompounds. Selenite was the predominant selenocompound found in vascular perfusate, but protein-bound Se was the predominant metabolite from selenite present in the vascular effluents. There was a corresponding increase of all metabolites with increased levels of selenite with time of absorption, but not with increased concentration of luminal selenite.