Association between homocysteine and blood pressure in the NHANES 2003-2006: the mediating role of Vitamin C.

Background: The yearly escalation in hypertension prevalence signifies a noteworthy public health challenge. Adhering to a nutritious diet is crucial for enhancing the quality of life among individuals managing hypertension. However, the relationship between vitamin C and hypertension, as well as homocysteine, remains unclear. Objective: The primary aim of this investigation was to scrutinize the potential mediating role of Vitamin C in the association between homocysteine levels and blood pressure, utilizing data extracted from the National Health and Nutrition Examination Survey (NHANES) database. Methods: A total of 7,327 participants from the NHANES 2003-2006 were enrolled in this cross-sectional survey. The main information was obtained using homocysteine, Vitamin C, systolic blood pressure (SBP) and diastolic blood pressure (DBP). Correlation analysis was used to assess the correlation between homocysteine, SBP, DBP and vitamin C. Linear regression analysis was utilized to determine the ß value (ß) along with its 95% confidence intervals (CIs). Mediation analysis was performed to investigate whether the relationship between homocysteine and blood pressure was mediated by Vitamin C, and to quantify the extent to which Vitamin C contributed to this association. Results: The results manifested that the homocysteine was positively associated with SBP (r = 0.24, p < 0.001) and DBP (r = 0.03, p < 0.05), while negatively correlated with Vitamin C (r = -0.008, p < 0.001). Vitamin C was found to be negatively associated with SBP (r = -0.03, p < 0.05) and DBP (r = 0.11, p < 0.001). Mediation effect analysis revealed that a partial mediation (indirect effect: 0.0247[0.0108-0.0455], p < 0.001) role accounting for 11.5% of total effect, among homocysteine and SBP. However, the mediating effect of Vitamin C between homocysteine and DBP was not statistically significant. Conclusion: Hypertension patients should pay attention to homocysteine and Vitamin C level. What is more, hypertension patients ought to formulate interventions for Vitamin C supplementation as well as homocysteine reduce strategies to lower blood pressure.

The positivity rates and drug resistance patterns of Mycobacterium tuberculosis using nucleotide MALDI-TOF MS assay among suspected tuberculosis patients in Shandong, China: a multi-center prospective study.

Objective: To investigate the positivity rates and drug resistance characteristics of Mycobacterium tuberculosis (MTB) among suspected tuberculosis (TB) patients in Shandong Province, the second-largest population province in China. Methods: A prospective, multi-center study was conducted from April 2022 to June 2023. Pathogen and drug resistance were identified using nucleotide matrix-assisted laser desorption ionization time-of-flight mass spectrometry (nucleotide MALDI-TOF MS). Results: Of 940 suspected TB patients included in this study, 552 cases were found to be infected with MTB giving an overall positivity rate of 58.72%. Total of 346 cases were resistant to arbitrary anti-TB drug (62.68%), with Zibo (76.47%), Liaocheng and Weihai (both 69.23%) ranking top three and TB treatment history might be a related factor. Monoresistance was the most common pattern (33.53%), with isoniazid the highest at 12.43%, followed by rifampicin at 9.54%. Further analysis of gene mutations conferring resistance revealed diverse types with high heteroresistance rate found in multiple anti-TB drugs. Conclusion: A relatively high rate of MTB positivity and drug resistance was found in Shandong Province during and after the COVID-19 pandemic, indicating the need for strengthening rapid identification of species and drug resistance among suspected TB patients to guide better medication and minimize the occurrence of drug resistance.

Superabsorbent carboxymethyl cellulose-based hydrogel fabricated by liquid-metal-induced double crosslinking polymerisation.

Herein, we introduced a liquid-metal/polymerisable deep eutectic solvent (LM/PDES) system to the carboxymethyl cellulose (CMC) and acrylic acid solution to prepare a double-cross-linked CMC-polyacrylic acid (PAA)-LM/PDES superabsorbent hydrogel via graft crosslinking polymerisation for 5 min. FTIR and XRD provided evidence for the coordinate crosslinking between Ga3+ and carboxy groups in the CMC-PAA-LM/PDES gel structure and chemical crosslinking between CMC and PAA components. The pore size of the obtained hydrogels gradually decreases with the increase of LM-AA/PDES content. The rigid CMC polysaccharide chains increased the distance between the ionic groups on the flexible PAA molecular chains, resulting in high osmotic pressure. In addition, the synergistic effects of hydrophilic groups, electrostatic repulsion, macroporous structures and double crosslinking on the CMC and PAA structures provided a driving force and space for the gel to absorb electrolyte containing liquid. The absorption capacity of the CMC-PAA-LM/PDES gel for physiological saline reached 97 g/g, which exceeded that of a single cross-linked CMC-PAA gel and a reported superabsorbent material (71 g/g). This work solved the problem of long heating times and insufficient mechanical properties for the preparation of superabsorbent gels, providing a theoretical reference for improving the absorption capacity of superabsorbent materials for electrolyte-containing aqueous solutions.

Recent studies on proteins and polysaccharides-based pH-responsive fluorescent materials.

Polymer-based pH-responsive fluorescent materials have the characteristics of fast response, real-time monitoring, visualisation, and easy forming. Consequently, they have attracted widespread attention in wound healing, sweat monitoring, security and anti-counterfeiting, freshness detection of aquatic products, metal-ion sensing and bioimaging. This paper analyses the preparation principles and characteristics of pH-responsive fluorescent materials based on cellulose, chitosan and proteins. It then outlines the fluorescence properties, environmental response mechanisms and applications of various luminescent materials. Next, the research indicates that amines, N-heterocyclic rings, carboxyl groups and amino plasmonic groups on the fluorescent molecule structure and polymer skeleton appear to change the degree of ionisation under acid or alkali stimulation, which affects the light absorption ability of chromophore electrons, thus producing fluorescence changes in fluorescent materials under different pH stimuli. On this basis, the challenges and growth encountered in the development of proteins and polysaccharides-based pH-responsive fluorescent materials were prospected to provide theoretical references and technical support for constructing pH-responsive fluorescent materials with high stability, high sensitivity, long-lasting pH-response and wide detection range.

Lycium barbarum polysaccharide protects cardiomyocytes from hypoxia/reoxygenation injury via activation of SIRT3/CypD signaling.

Background: Myocardial ischemia-reperfusion is a common pathological feature of many heart and vascular diseases, but the molecular mechanism of this process is still unclear, and there is no effective way to protect cardiomyocytes. The aim of this study was to examine the effects and underlying molecular mechanisms of Lycium barbarum polysaccharide (LBP) on myocardial ischemia-reperfusion injury in cardiomyocytes. Methods: The cardiomyocyte cell line H9c2 were used to establish an in vitro hypoxia/reoxygenation (H/R) model. After treatment with LBP and/or the SIRT3 inhibitor 3-TYP, cell morphology was observed under the light microscopy. The Cell Counting Kit (CCK)-8 and 5-ethynyl-2'-deoxyuridine (EdU) assay were used to detect cell proliferation, and flow cytometry was performed to assess cell apoptosis. The lysine (166)-acetylation of CypD1 was determined by co-immunoprecipitation assay. Enzyme-linked immunosorbent assay (ELISA) was used to determine the lactate dehydrogenase (LDH) level in the culture medium. Na+-K+-ATPase activity, Ca2+-ATPase activity, and nitric oxide (NO) levels were measured. Results: LBP alleviated cell damage and upregulated STIR3 expression in a dose-dependent manner. Upregulated SIRT3 expression and suppressed acetylation of CypD were also observed in H/R-induced H9c2 cells treated with LBP. Indeed, LBP remarkably reversed the inhibition of proliferation and cell apoptosis in H/R-induced H9c2 cells by activating SIRT3/CypD signaling. Blockade of SIRT3 with SIRT3 inhibitor (3-TYP) inhibited the protective effect of LBP on H9c2 cells. LBP markedly alleviated the H/R-induced increase of LDH release, and the decrease of Na+-K+-ATPase activity, Ca2+-ATPase activity, and NO levels. Inhibition of SIRT3 restored the protective effects of LBP. Conclusions: LPB induced deacetylation of CypD by upregulating SIRT3, thereby protecting mitochondrial function and relieving H/R-induced injury in cardiomyocytes.

A Novel Deep Learning Method Based on an Overlapping Time Window Strategy for Brain-Computer Interface-Based Stroke Rehabilitation.

Globally, stroke is a leading cause of death and disability. The classification of motor intentions using brain activity is an important task in the rehabilitation of stroke patients using brain-computer interfaces (BCIs). This paper presents a new method for model training in EEG-based BCI rehabilitation by using overlapping time windows. For this aim, three different models, a convolutional neural network (CNN), graph isomorphism network (GIN), and long short-term memory (LSTM), are used for performing the classification task of motor attempt (MA). We conducted several experiments with different time window lengths, and the results showed that the deep learning approach based on overlapping time windows achieved improvements in classification accuracy, with the LSTM combined vote-counting strategy (VS) having achieved the highest average classification accuracy of 90.3% when the window size was 70. The results verified that the overlapping time window strategy is useful for increasing the efficiency of BCI rehabilitation.

Development of Environmentally Friendly Wool Shrink-Proof Finishing Technology Based on L-Cysteine/Protease Treatment Solution System.

The particular scale structure and mechanical properties of wool fiber make its associated fabrics prone to felting, seriously affecting the service life of wool products. Although the existing Chlorine-Hercosett treatment has a remarkable effect, it can lead to environmental pollution. Therefore, it is of great significance to develop an environmentally friendly and effective shrink-proof finishing technology. For this study, L-cysteine was mixed with protease to form a treatment solution system for shrink-proof finishing of wool fibers. The reduction performance of L-cysteine and its effect on wool were compared with those of other reagents, demonstrating that L-cysteine has an obvious reduction and destruction effect on the wool scale layer. Based on this, L-cysteine and protease 16L were mixed in a certain proportion to prepare an L-cysteine/protease treatment solution system (L/PTSS). The shrink-proof finishing of a wool top was carried out by the continuous multiple-padding method, and the processing parameters were optimized using the response surface method. The results indicated that when the concentrations of L-cysteine and protease 16L were 9 g/L and 1 g/L, respectively, the wool was padded five times at 50 °C, and each immersion time was 30 s, the felt ball density of the treated wool reduced from 135.86 kg/m3 to 48.65 kg/m3. The structure and properties of the treated wool were also characterized using SEM, TG, and tensile strength tests, which indicated that the fiber scale structure was stripped evenly. Meanwhile, the treated fibers still retained adequate thermal and mechanical properties, indicating suitable application value. XPS, FT-IR, Raman, UV absorbance, and other test results revealed the reaction mechanism of L/PTSS with the wool fibers. After L-cysteine rapidly reduced the disulfide bonds in wool, protease can hydrolyze peptide chains more effectively, causing the scale layer to gradually peel off. Compared with the chlorination method and other protease shrink-proof technologies, L/PTSS can achieve the finishing effect on wool rapidly and effectively, without causing excessive pollution to the environment. The conclusions of this study provide a foundation for the development and industrial application of biological enzyme shrink-proof finishing technology.

Characterization of the keratin/polyamide 6 composite fiber's structure and performance prepared by the optimized spinning process based on the rheological analysis.

The complex chemical structure of polypeptide and the imperfection of processing technology cause the mechanical properties of regenerated keratin to be hard and brittle. This defect seriously affects the application prospects of keratin materials. To solve the above problems, α-lipoic acid modified keratin (KER) was blended with Polyamide 6 (PA6) and prepared into composite fibers via the wet-spinning method in this work. The spinnability and spinning conditions of the KER/PA6 blend solution were analyzed by rheological theory. The results illustrated that keratin solution will easily form a gel state under certain temperatures and concentrations, which was not conducive to the preparation of regenerated fiber. When the temperature was 45 °C and the mass fraction was 10 %, the viscosity and rheology of the solution were appropriate. The rheological properties of the blend solution showed that too much keratin would make the solution easy to gel, which was not conducive to the preparation of regenerated fibers and may affect the fiber properties. On this basis, the prepared composite fibers were characterized to explore the macromolecular aggregation state of keratin and PA6 in fibers. FT-IR and XRD results proved that there was no chemical reaction between keratin and PA6 in the composite fibers, which belonged to physical blending. At the same time, the two polymers had good compatibility and can be blended at the molecular level. SEM, DSC, and tensile strength test results indicated that when the proportion of keratin was too high, the structure and properties of the composite fibers will have obvious defects, which was consistent with the rheological analysis. Therefore, the blend ratio of keratin/PA6 was determined to be 3:7. Under this condition, the fibers exhibited a homogeneous structure and good thermal properties, especially its mechanical properties were close to wool fibers. The KER/PA6 composite fibers show important research value and can also provide technical reference for the development of regenerated biomass materials.

Adsorption-enhanced photocatalytic property of Ag-doped biochar/g-C3N4/TiO2 composite by incorporating cotton-based biochar.

In this study, the biochar obtained from waste cotton fibers was introduced into the Ag-doped g-C3N4/TiO2 hybrid composite through a facile one-step hydrothermal process. The morphology, elemental composition, crystal structure, microstructure, specific surface area, chemical bonding state, energy band structure, and separation efficiency of photoinduced charge carriers of the resultant composite were examined using scanning electron microscope, energy dispersive X-ray spectrometer, X-ray diffractometer, transmission electron microscope, surface area analyzer, X-ray photoelectron spectroscope, Ultraviolet-visible spectrophotometer, ultraviolet photoelectron spectroscope, and photoluminescence spectroscope. The adsorption isotherms, kinetics and thermodynamics of the biochar, Ag-doped g-C3N4/TiO2 and Ag-doped biochar/g-C3N4/TiO2 were evaluated using the model methyl orange dye. The photoacatalytic degradation of the model pollutants including methyl orange, methylene blue, congo red, and tetracycline hydrochloride and the photocatalytic reduction of Cr(VI) ions were also assessed under visible light. Experimental results indicated that the photocatalytic property of the Ag-doped biochar/g-C3N4/TiO2 was significantly enhanced through the adsorption enhancement compared with the Ag-doped g-C3N4/TiO2. This was due to the uniform doping of multi-scale porous biochar with g-C3N4 nanosheet, Ag and TiO2 nanoparticles. The adsorptive enhancement induced by the biochar resulted in the narrowed band gap, suitable electronic energy band structure, and fast separation of photoinduced charge carriers of the Ag-doped biochar/g-C3N4/TiO2, which was probably due to the coexistence of multi-valence Ti+4/+3 and Ag0/+1 species and oxygen-containing groups of biochar. The major reactive species of the Ag-doped biochar/g-C3N4/TiO2 were 1O2 and h+. The MO dye adsorption onto the Ag-doped biochar/g-C3N4/TiO2 followed the Langmuir isotherm model, pseudo-first-order and pseudo-second-order kinetic models, and the adsorption process was an endothermic reaction with entropy reduction effects. As such, the Ag-doped biochar/g-C3N4/TiO2 exhibited a promising application for the treatment of wastewater containing multi-pollutants especially organic dyes and heavy metal ions.

Facile synthesis of self-dispersed ß-cyclodextrin-coupled cellulose microgel for sustained release of vanillin.

A self-dispersed ß-cyclodextrin-coupled cellulose (ß-CD-Cel) microgel was firstly synthesized via chemically coupling cellulose and ß-CD in NaOH/urea aqueous solution. Following, after encapsulating the hydrophobic vanillin molecules into the cavities of ß-CD-Cel microgel through host-guest interaction, cellulose-based long-lasting fragrance-released complex was obtained. ß-CD was mainly bonded onto the hydroxyl groups at C6 in the AGU units of cellulose, and about 0.5 ß-CD molecule were introduced into the AGU unit when cellulose skeleton contained the ß-CD content of 19.33%. FTIR, 1H NMR, XRD, and UV-Vis provided evidences for the encapsulation of vanillin in the cavity of ß-CD-Cel, and the encapsulating efficiency of vanillin for the ß-CD-Cel inclusion complex was upped to 86.9%, which exceeded that of single ß-CD small molecule encapsulating fragrance. Benefiting from the reversible host-guest interaction between ß-CD and vanillin molecule, the continuous fragrance release time could exceed 196 h, and the sustained release behavior of ß-CD-Cel complex could be adjusted by temperature. Also, the fragrance-released ß-CD-Cel composite film showed high transparency, strong water resistance, and good flexibility. The vanillin retention of the composite film can keep 40% after soaking in ethanol solution for 96 h. This study will provide a new approach for the development of biomass functional coating.

pH-Responsive Dual-Emitting Hydroxypropyl Methylcellulose-Based Material Containing Fluorescein Isothiocyanate and CaAl2O4:Eu2+,Dy3+ Phosphors.

Herein, we prepared a dual-emitting cellulose film with pH response, which offers high transparency, good flexibility, and intense thermal stability. The color of the fluorescent film that changes from green to blue-green to cyan was achieved by covalently attaching organic dye fluorescein isothiocyanate (FITC), inorganic pigment NH2-CaAl2O4:Eu2+,Dy3+ (NH2-CAO), and organic-inorganic fluorescence species onto hydroxypropyl methylcellulose (HMPC) chains, respectively. Benefiting from the "anchoring" and "dilution" effects of the HMPC skeleton, HPMC-FITC and HPMC@NH2-CAO fluorescent solutions and solid-state films emit green and blue-green fluorescence at 535 and 480 nm, respectively. The obtained pH-responsive cellulose-based dual-emitting film can continuously emit cyan light at the two emission peaks of 480 and 535 nm for a long time and exhibits strong fluorescence intensity under exceedingly alkaline conditions. Moreover, the HPMC-based fluorescent solution coated on glass and fabric substrate shows strong fluorescence under 365 nm UV light stimulation. Compared with the existing cellulose-based fluorescent films, this work expands the emission wavelength range of cellulose-based fluorescent films and prolongs the luminescent time of environment-responsive fluorescent films. This provides a new way to prepare intelligent color-changing fabric-coating materials and sensitive pH sensors based on biomass.

Morphology-controllable amphiphilic cellulose microgels made from self-assembly of hydrophobic long-chain bromide-alkylated-cellulose/gelatin copolymer.

A cellulose-based microgel is firstly synthesized via chemically coupling gelatin and cellulose, and then amphiphilic cellulose copolymers (HMGC) are prepared by alkylated cellulose-based microgel from different long-chain alkyl groups. The long-chain alkyl group is mainly bonded onto the residual hydroxyl group at C6 from the AGU of cellulose and the imino groups of gelatin, respectively. The results of self-assembly behavior of HMGC demonstrate that the critical aggregation concentrations of the microgels are in the range from 0.628 to 0.075 mg/mL, and the corresponding hydrodynamic diameters are between 104-1000 nm. Besides, the HMGC can self-assemble into microgels of various morphologies including cotton flocculence, sphere, rod-like, vesicle, flower-like cluster, snowflake-like, urchin-like, and coral shapes. These novel morphologies can be controlled by adjusting the degree of alkylation, the length of the alkyl chain, and the concentration of microgel. Furthermore, the possible formation mechanism of the multiform microgels is proposed from the chain conformation.

Magnetically Recyclable Wool Keratin Modified Magnetite Powders for Efficient Removal of Cu2+ Ions from Aqueous Solutions.

The treatment of wastewater containing heavy metals and the utilization of wool waste are very important for the sustainable development of textile mills. In this study, the wool keratin modified magnetite (Fe3O4) powders were fabricated by using wool waste via a co-precipitation technique for removal of Cu2+ ions from aqueous solutions. The morphology, chemical compositions, crystal structure, microstructure, magnetism properties, organic content, and specific surface area of as-fabricated powders were systematically characterized by various techniques including field emission scanning electron microscopy (FESEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), vibrating sample magnetometer (VSM), thermogravimetric (TG) analysis, and Brunauer-Emmett-Teller (BET) surface area analyzer. The effects of experimental parameters such as the volume of wool keratin hydrolysate, the dosage of powder, the initial Cu2+ ion concentration, and the pH value of solution on the adsorption capacity of Cu2+ ions by the powders were examined. The experimental results indicated that the Cu2+ ion adsorption performance of the wool keratin modified Fe3O4 powders exhibited much better than that of the chitosan modified ones with a maximum Cu2+ adsorption capacity of 27.4 mg/g under favorable conditions (0.05 g powders; 50 mL of 40 mg/L CuSO4; pH 5; temperature 293 K). The high adsorption capacity towards Cu2+ ions on the wool keratin modified Fe3O4 powders was primarily because of the strong surface complexation of -COOH and -NH2 functional groups of wool keratins with Cu2+ ions. The Cu2+ ion adsorption process on the wool keratin modified Fe3O4 powders followed the Temkin adsorption isotherm model and the intraparticle diffusion and pseudo-second-order adsorption kinetic models. After Cu2+ ion removal, the wool keratin modified Fe3O4 powders were easily separated using a magnet from aqueous solution and efficiently regenerated using 0.5 M ethylene diamine tetraacetic acid (EDTA)-H2SO4 eluting. The wool keratin modified Fe3O4 powders possessed good regenerative performance after five cycles. This study provided a feasible way to utilize waste wool textiles for preparing magnetic biomass-based adsorbents for the removal of heavy metal ions from aqueous solutions.

Highly transparent, writable and photoluminescent foldable polymer film: When fluorescent dyes or pigments join cellulose-based microgel.

We prepared a self-dispersed cellulose-based microgel via chemically bonding hydrophilic gelatin peptide chain onto cellulose glucose chain. Following, a variety of highly transparent, foldable, and writable photoluminescent polymer films was obtained through loading organic dyes and inorganic pigments onto cellulose-based microgel matrix, respectively. Benefiting from the coupling sites and network effect of microgel as well as the abundant hydroxyl, amino, and imino groups in its structure, the microgel containing organic dyes and inorganic pigments exhibit good dispersion and stability, and the resultant photoluminescent films emit bright yellow, orange, yellow-green, and blue-green fluorescence under UV light, respectively, especially the cellulose-based microgel stabilized inorganic alkaline earth aluminate hybrids exhibit continuous luminescence for a long time in the dark. Compared with the existing regenerated cellulose or CNCs-based fluorescent films, the cellulose-based microgel fluorescent films present higher transmittance and good biodegradability. This study can bring new ideas for the development of flexible luminescent devices.

Photocatalytic mechanism and performance of a novel wool flake-BiFeO3nanosheet-TiO2core-shell-structured composite photocatalyst.

In this study, BiFeO3(BFO) nanosheets ground from BFO particles were first incorporated with wool flakes to construct sandwich-like wool-BFO composites using the vibration-assisted ball milling technique in freezing conditions. The wool-BFO composites were then loaded with a thick layer of TiO2nanoparticles to prepare the core-shell-structured wool-BFO-TiO2composites using a hydrothermal synthesis process. The microstructure of the core-shell wool-BFO-TiO2composites and its photocatalytic applications were systematically examined using a series of characterization methods. Trapping experiments and electron spin resonance spectra were also employed to judge the active radical species like superoxide radicals (·O2-), singlet oxygen (1O2), holes (h+), and hydroxyl radicals (·OH) using benzoquinone, furfuryl alcohol, ethylenediamine tetraacetic acid, and tert-butanol as the scavengers, respectively. The photodegradation performance of the wool-BFO-TiO2composites was measured using more resistant methyl orange (MO) dye as the pollutant model. In comparison with the wool-TiO2or wool-BFO composites, the superior photocatalytic properties of the wool-BFO-TiO2composites under visible light irradiation were attributed to the presence of mesopores and macropores, the large specific surface area and intimate interface between wool-BFO composites and TiO2nanoparticles, the coexistence of Fe3+, Fe2+, Bi3+, Bi(3-x)+, Ti4+, and Ti3+species, and the strong visible light harvesting, thus leading to the fast separation of photogenerated electron-hole pairs. The wool-BFO-TiO2composites could be used for the repeated photodegradation of organic pollutants and be recycled easily using a magnet. The active radical species of the wool-BFO-TiO2composites were ·O2-and1O2rather than ·OH and h+, which were involved in the photodegradation of MO dye under visible light irradiation.

TiO2 modified orthocortical and paracortical cells having enhanced photocatalytic degradation and photoreduction properties.

In this study, cortical cells resultant from wool fibers were loaded with TiO2 nanoparticles in a hydrothermal process and were then engineered as organic-nonorganic hybrid composite photocatalysts for both photodegradation of organic dyes and photoreduction of heavy metal ions. The microstructure and photocatalytic properties of TiO2 modified cortical cells (i.e. both orthocortical and paracortical cells) were systematically characterized using a series of analytical techniques including FESEM, TEM, element analysis, Mott-Schottky curve, BET specific surface area, Zeta potentials, as well as XRD, FTIR, XPS, DRS, PL, UPS, EDS and ESR spectra. Their photocatalytic performance and trapping experiments of the TiO2 modified cortical cells were measured in the photodegradation of methylene blue (MB) dye and Congo Red (CR) dye as well as the photoreduction of Cr(VI) ions under visible light irradiation. It was found that anatase TiO2 nanoparticles were chemically grafted on the surface of the two cortical cells via O-Ti4+/O-Ti3+ bonds, and that TiO2 nanoparticles were formed inside the orthocortical cells in the hydrothermal process. The TiO2 modified orthocortical and paracortical cells possessed much higher photocatalytic efficiency than the commercially available TiO2 nanoparticle powder, Degussa P25, in the photodegradation of cationic MB dye and photoreduction of Cr(VI) ions, while their photocatalytic efficiency in the photodegradation of anionic CR dye is smaller because of their greater negative Zeta potentials and photogenerated holes as the main reactive radical species. In comparison with the TiO2 modified paracortical cells, the higher photocatalytic efficiency of the TiO2 modified orthocortical cells was demonstrated in the photodegradation of MB dye solution and this might be due to both the S-doped TiO2 nanoparticles infiltrated into the naturally hydrophilic orthocortical cells and the primary reactive radical species of photogenerated holes being trapped in the cells.

Enhanced Photocatalytic Properties of PET Filaments Coated with Ag-N Co-Doped TiO2 Nanoparticles Sensitized with Disperse Blue Dyes.

In this study, the effects of disperse blue dye-sensitization on the photocatalytic properties of the Ag-N co-doped TiO2 nanoparticles loaded on polyethylene terephthalate (PET) filaments are investigated under visible light irradiation. The microstructure and photocatalytic properties of the as-synthesized TiO2 nanocomposites, as well as the as-prepared PET filaments, are systematically characterized. The photocatalytic performance of the PET filaments coated with the Ag-N co-doped TiO2 nanoparticles sensitized with disperse blue dyes is evaluated via its capacity of photo-degrading methyl orange (MO) dyes under visible light irradiation. It is found that the holes are the predominant reactive radical species and the hydroxyl and superoxide radicals play a subordinate role in the photocatalytic reaction process. The reaction rate constant of the photocatalytic composite filaments is nearly 4.0 times higher than that of the PET filaments loaded solely with TiO2 nanoparticles. The resultant photocatalytic composite filaments are evident to be capable of repeatedly photo-degrading MO dyes without losing its photocatalytic activity significantly.

Effects of Temperature on Bending Properties of Three-Dimensional and Five-Directional Braided Composite.

The bending properties of three-dimensional (3Dim) and five-directional (5Dir) braided/epoxy resin composites at room temperature, 90 °C, 110 °C, and 150 °C and heating for 0.25 h, 10 h, and 30 h, respectively, were studied. The effect of different temperatures and heating times on the bending property of these composites was discussed. The results showed that the bending strength of these composites at 90 °C, 110 °C, and 150 °C and heating time of 0.25 h is 33.86%, 46.27%, and 83.94% lower, respectively, than that at room temperature. In addition, 3Dim-5Dir braided composites exhibit different damage modes at different temperatures, revealing different failure mechanisms. Heating temperature has greater influence on the bending properties of these composites than heating time. The results provided a basis for the application of resin-based 3Dim-5Dir braided/epoxy resin composites at different temperatures.

Enhanced photocatalytic activity of wool fibers having titanium dioxide nanoparticles formed inside their cortex.

A wool-TiO2 nanoparticle composite material having TiO2 nanoparticles both infiltrated in the matrix between macrofibrils inside cortical cells of wool fibers and grafted on the fiber surface is obtained in this study, and the wool-nanoparticle composite material is found to have highly photocatalytic activities with an extremely narrow band gap of 2.8 eV. The wool fibers are obtained using three successive technical steps: wool fibers are swollen by using lithium bromide, then saturated with tetrabutyl titanate ethanol solution and subsequently treated in boiling water. It was demonstrated that the chemical bonds formed between the as-synthesized TiO2 nanoparticles and the wool fibers swollen by lithium bromide include C-Ti4+(Ti3+), N-Ti4+(Ti3+), O-Ti3+, and S-Ti4+(Ti3+) bonds. The modified wool fibers have shown markedly improved photocatalytic efficiency due to their enhanced visible light absorption capability, which is much better than the (N-doped) TiO2 coated wool fibers. In contrast, TiO2 modified wool fibers swollen by using formic acid have poorer photoactivity, this might be due to the elimination of trivalent titanium between TiO2 nanoparticles and the wool fibers.

Association between Aqueous Cytokines and Diabetic Retinopathy Stage.

PURPOSE: To measure the concentrations of various cytokines in the aqueous humor from patients with different stages of diabetic retinopathy. METHODS: All selected cataract patients were categorized into 4 groups: the control group (patients without diabetes), nonretinopathy (NDR) group (diabetic patients without retinopathy), nonproliferative diabetic retinopathy (NPDR) group, and proliferative diabetic retinopathy (PDR) group. The aqueous concentrations of interleukin- (IL-) 1ß, IL-2, IL-4, IL-5, IL-6, IL-10, interferon-γ, tumor necrosis factor-α, and vascular endothelial growth factor (VEGF) from patients were measured using the cytometric bead array technique. RESULTS: In this study, 10, 22, 15, and 14 patients were included in the control, NDR, NPDR, and PDR groups, respectively. No difference was observed in the aqueous concentrations of all cytokines between the control group and the NDR group. By contrast, comparison of these groups revealed that the aqueous concentrations of most inflammatory cytokines were significantly higher in the PDR and NPDR groups. In addition, the concentrations of IL-2, IL-5, and VEGF were higher in the PDR group than those in the NPDR group. CONCLUSIONS: Aqueous concentrations of various cytokines increased with the severity of patients' diabetic retinopathy. This finding implies that these cytokines might play a role in the progression of diabetic retinopathy.