Si-rhodamine fluorescent probe for monitoring of hypochlorous acid in the brains of mice afflicted with neuroinflammation.

Neuroinflammation leads to a persistent oxidative stress in the brain, and is closely related to the pathology of various neurological disorders. Hypochlorous acid (HClO) is a reactive oxygen species (ROS) that, at high levels, can cause brain tissue damage and neurogenic apoptosis. Herein, we designed and synthesized a silicon-rhodamine (SiR)-based formohydrazide (FH)-containing fluorescent probe, denoted as SiR-FH, for sensing HClO. This probe showed good selectivity, rapid response and high sensitivity. SiR-FH was successfully used to detect endogenous and exogenous HClO in living cells. Moreover, SiR-FH realized real-time monitoring of change in HClO flux in the brains of mice with LPS-induced neuroinflammation. The probe provides a practical tool for the monitoring of oxidative stress related to neuroinflammation.

A novel near-infrared fluorescence probe for detecting and imaging Hg2+ in living cells.

Fluorescence imaging, as one of the important means of biological lesion analysis, is widely used in medical analysis. To improve detection specificity, near-infrared emission fluorescent probes have been developed. Sensitive and selective near-infrared (NIR) fluorescent probes for Hg2+ , which is a heavy metal ion harmful to human health, are urgently needed to investigate the physiological toxicity of Hg2+ . The NIR fluorophore based on the traditional structure of rhodamine was prepared by introducing anthocyanin functional groups, and a rhodamine spiro ring structure was constructed to recognize Hg2+ (CCS-Hg). The probe CCS-Hg demonstrated good selectivity and high detection sensitivity for Hg2+ and the most likely mechanism was verified through theoretical calculations. We applied the probe CCS-Hg in the examination of Hg2+ distribution in living cells by NIR fluorescence imaging. This work provides a promising molecular tool for studying the toxicological effects of mercury ions in cell.

Vortex-assisted solid-phase extraction based on metal-organic framework/chitosan-functionalized hydrophilic sponge column for determination of triazine herbicides in environmental water by liquid chromatography-tandem mass spectrometry.

In the presented work, MIL-101(Cr) and chitosan were directly embedded on the skeleton of melamine sponge material using a simple and environmentally friendly method. Chitosan acts not only as an adhesive during the preparation of functionalized sponges, but also as an adsorption adjuvant in herbicide detection. Unlike other polymers, chitosan has excellent hydrophilicity and contains numerous adsorption sites; thus, it enables the sponge material to be used for determination of contaminants in an aqueous phase. Scanning electron microscopic (SEM) analysis showed that the coating material was uniformly distributed on the skeleton of melamine sponge. The prepared material was used as a sorbent in a vortex-assisted solid-phase extraction and combined with high performance liquid phase tandem mass spectrometry for the extraction and trace determination of six triazines in water samples (Atraton, Desmetryn, Prometon, Ametryn, Prometryn and Dimethametryn). Several parameters that affect the extraction efficiencies were investigated. Under the optimal conditions (MIL-101(Cr) loading, 150 mg; sample pH, 7; salt concentration, 0%; adsorption time, 3 min; desorption solvent, 1.5 mL acetonitrile; desorption time, 4 min), the proposed method was successfully used in the determination of trace triazines in five real water samples (drinking water, tap water, lake waters and river water), satisfactory recoveries were obtained in the range of 78.9%-118.6%. The limits of detection of the proposed method in detecting triazine herbicides in spiked water samples ranged from 0.014 to 0.045 ng mL-1.

A novel near-infrared fluorescent probe for the dynamic monitoring of the concentration of glutathione in living cells.

In this study, a water-soluble, near-infrared fluorescent probe (EQR-S) was designed for the measurement of the glutathione (GSH) concentration. Responses of different interfering substances to the developed probe were investigated, and the luminescence mechanism was examined by theoretical calculations. Results revealed that EQR-S can be applied for the rapid, sensitive determination of the GSH concentration with a detection limit of 69 nM. Based on the above advantages, EQR-S was successfully applied to investigate the fluctuation in the GSH concentration of living cells under high-temperature stress.

Grazing exclusion promotes grasses functional group dominance via increasing of bud banks in steppe community.

To understand the bud banks response to grazing exclusion, we conducted a demographic experiment in long-term grazing exclusion (20 year and 30 year) typical steppe. Results showed that grass functional group constituted the vast majority of the aboveground vegetation and belowground bud bank in all treatments. Long-term grazing exclusion significantly increased total aboveground biomass (2.5 and 2.6 times in 20y and 30y grazing exclusion grasslands, respectively), and decreased total stem density (31% and 37% in 20y and 30y grazing exclusion grasslands, respectively). Grazing exclusion for 20 and 30 years increased grass aboveground biomass respectively by 6.0 and 8.0 times, and decreased grass stem density by 38% and 33%. Grazing exclusion had different effects on belowground bud density of grass and forb functional group. Long-term grazing exclusion significantly increased plant buds and bud bank size (25% and 37% in 20y and 30y grazing exclusion grasslands, respectively), especially for grass functional group (49% and 95% in 20y and 30y grazing exclusion grasslands, respectively), but had no significant effects on forb bud density. Changes of aboveground community were significantly related to changes of belowground bud bank under both grazing and grazing exclusion grasslands. The bud bank density of grass functional group was significantly positive with total (R2 = 0.33, P < 0.05) and grass aboveground biomass (R2 = 0.36, P < 0.01), while negative related with total (R2 = -0.27, P < 0.05) and grass stem density (R2 = -0.22, P < 0.05). Grazed grasslands, 20y and 30y grazing exclusion grasslands all were not meristem limited and had large reserve bud banks, which would completely replace the aboveground stem population during the growing season. These findings indicate that grazing exclusion could not only improve a large bud bank for grassland restoration but also improve the dominance of grass functional group by increasing grass belowground bud banks in typical steppe community. We propose that the belowground bud bank might be a good approach to indicating potential succession direction of aboveground community.

Determination of hormones in milk by hollow fiber-based stirring extraction bar liquid-liquid microextraction gas chromatography mass spectrometry.

The hollow fiber-based stirring extraction bar liquid-liquid microextraction was applied to the extraction of hormones, including 17-α-ethinylestradiol, 17-α-estradiol, estriol, 17-ß-estradiol, estrone, 17-α-hydroxyprogesterone, medroxyprogesterone, progesterone and norethisterone acetate, in milk. The present method has the advantages of both hollow fiber-liquid phase microextraction and stirring bar sorptive extraction. The stirring extraction bar was used as both the stirring bar of microextraction, and extractor of the analytes, which can make extraction, clean-up and concentration be carried out in one step. When the extraction was completed, the stirring extraction bar was easy isolated from the extraction system with the magnet. Several experimental parameters, including the type of extraction solvent, the number of hollow stirring extraction bar, extraction time, stirring speed, ionic strength, and desorption conditions were investigated and optimized. The analytes in the extract were derived and determined by gas chromatography mass spectrometry. Under optimal experimental conditions, good linearity was observed in the range of 0.20-20.00ng mL(-1). The limits of detection and quantification were in the range of 0.02-0.06ng mL(-1) and 0.07-0.19ng mL(-1), respectively. The present method was applied to the analysis of milk samples, and the recoveries of analytes were in the range of 93.6-104.6% with the relative standard deviations ranging from 1.6% to 6.2% (n=5). The results showed that the present method was a rapid and feasible method for the determination of hormones in milk samples.

Implanting hydroxyapatite-coated porous titanium with bone morphogenetic protein-2 and hyaluronic acid into distal femoral metaphysis of rabbits.

OBJECTIVE: To assess the osseointegration capability of hydroxyapatite-coated porous titanium with bone morphogenetic protein-2 (BMP-2) and hyaluronic acid to repair defects in the distal femur metaphysis in rabbits. METHODS: Porous titanium implants were made by sintering titanium powder at high temperature, which were coated with hydroxyapatite by alkali and heat treatment and with BMP-2 combined with bone regeneration materials. And hyaluronic acid was further used as delivery system to prolong the effect of BMP-2. The implants were inserted into the metaphysis of the distal femur of rabbits. The animals were killed at 6, 12 and 24 weeks to accomplish histological and biomechanical analyses. RESULTS: According to the result of histological analysis, the osseointegration in BMP-2 group was better than that of the HA-coated porous titanium group. In push-out test, all the samples had bigger shear stress as time passed by. There was statistical difference between the two groups in 6 and 12 weeks but not in 24 weeks. CONCLUSION: Hydroxyapatite-coated porous titanium with BMP-2 and hyaluronic acid has a good effect in repairing defects of distal femur in rabbits, which is a fine biotechnology for future clinical application.

Investigation on hyperin-cetyltrimethylammonium bromide-fibronectin system by resonance light-scattering technique.

A simple, highly sensitive assay for fibronectin (Fn) was reported using resonance light-scattering (RLS) technique based on the enhanced RLS intensity of hyperin-cetyltrimethylammonium bromide (CTMAB)-Fn system. The interaction system of hyperin-CTMAB-Fn was investigated using spectral methods. Mechanistic investigations show that the main reason of the enhanced RLS intensity of Fn is the formation of three-component complex (hyperin-CTMAB-Fn), in which CTMAB acts as a bridge between hyperin and Fn. The effects of pH, surfactant, concentration of CTMAB and hyperin, incubation time and foreign substances on the enhancement of RLS intensity were studied. Under the optimum conditions, the enhancement of RLS intensity is in proportion to the concentration of Fn in the range of 1.9-248ng/ml. The synthetic samples containing Fn were analyzed and results obtained were satisfied.

Investigation on the interaction between colloidal gold and human complement factor 4 at different pH by spectral methods.

The interaction between colloidal gold and human complement factor 4 (human C4) at different pH was investigated by spectral methods, including absorption and resonance light-scattering spectrometry. According to the changes of color and absorption spectra of colloidal gold solution in presence of human C4, the interaction between colloidal gold and human C4 was quantitatively investigated using a semi-empirical "flocculation parameter". At the same time, the changes of resonance light-scattering spectra and transmission electron microscopy (TEM) images indicate that the aggregation of colloidal gold happens by electrostatic interaction in presence of human C4 in the pH range 5-6. However, the colloidal gold solution remains stable at pH >6 and pH <5 due to the repulsive electrostatic interaction between colloidal gold and human C4. The flocculation parameter is directly proportional to the concentration of human C4 in the range from 9.7 to 233.0 microgl(-1). In addition, the interactions between the colloidal gold and bovine serum albumin (BSA) as well as human serum albumin (HSA) were also investigated using the same methods. It was found that there was no aggregation of colloidal gold in presence of BSA and HSA in the pH range 5-6. However, when the pH of solution is 4, the aggregation of colloidal gold happens. Because BSA and HSA have different structure, the intensity of aggregation of colloidal gold in presence of BSA is greater than that in presence of HSA at pH 4.

Determination of human complement factor C4 using resonance light-scattering technique with sodium dodecylbenzene sulphonate probe.

Based on the interaction between human complement factor C4 (human C4) and sodium dodecylbenzene sulphonate (SDBS) and the resonance light-scattering (RLS) technique, a highly sensitive assay for human C4 using resonance light-scattering technique was developed. At pH 2.8 Na2HPO4-citric acid buffer solution, the RLS intensities of SDBS system at 283, 503 and 600 nm were obviously enhanced in the presence of human C4. The effects of surfactant, pH, incubation time, concentration of SDBS and foreign substances on the enhanced RLS intensity of system were investigated. Under the optimum conditions, the enhanced RLS intensity is directly proportional to the concentration of human C4 in the range of (0.5-120)x10(-6)gl-1 and the linear regression equation was obtained with high correlation coefficient. This RLS technique was applied to the determination of human C4 in some synthetic samples with good recovery. Moreover, it was found that the electrostatic interaction is the main binding force between SDBS and human C4.