Synthesis of azo-linked covalent organic polymers for pipette tip solid-phase extraction of sedative residues from animal tissues samples.

Azo-linked covalent organic polymers (ACOPs) were synthesized by a simple azo reaction, with 2,2'-bis(trifluoromethyl)benzidine and 1,3,5-trihydroxybenzene as the monomers. The preparation process was mild, green, and environmental-friendly, avoiding the use of high temperature, metal catalysis, and harmful organic reagent. The obtained ACOPs were characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, thermogravimetric analysis, powder X-ray diffraction, and Brunauer-Emmett-Teller. With the prepared ACOPs as adsorbent, a method of pipette tip solid-phase extraction-liquid chromatography-tandem mass spectrometry detection (PTSPE-LC-MS/MS) was proposed for the analysis of target sedatives in animal tissues. Furthermore, the parameters for the extraction of five sedatives, including the amount of adsorbent, pH value, ion strength, elution solvent and volume, were investigated. Under the optimized conditions, the linear dynamic range was found from 0.1 to 10.0 µg kg-1, and the limits of detection were ranged from 0.02 to 0.1 µg kg-1. The method was assessed by the analysis of target sedatives in animal tissues, and the recoveries for the spiked pork muscle and pork liver samples were 84-102% and 83-101%, respectively. The results show that the developed method of PTSPE-LC-MS/MS with ACOPs as adsorbent is efficient for the analysis of trace sedatives in animal tissues.

Detection of azithromycin residue in broiler feathers by liquid chromatography-tandem mass spectrometry.

In the study, a sensitive and reproducible method for the quantitative analysis of azithromycin in broiler feather samples by liquid chromatography-tandem mass spectrometry (LC-MS/MS) was developed. Feather samples were rinsed after being wrapped in medical gauze, then chopped and then added to 5% (v/v) ammonia in methanol solution for ultrasonic extraction. The extract was purified by the combination of commercial polymeric microparticles (Oasis MCX) and Fe3O4 nanoparticles. The LC separation was performed on an Agilent Eclipse plus C18 column. Multiple reaction monitoring was used for the selective detection of azithromycin. The good linearity curve of azithromycin in feather sample was in the range from 1.0 µg kg-1 to 100.0 µg kg-1 with 0.9935 of correlation coefficient. And the limit detection and limit of quantification was 0.5 µg kg-1 and 2.0 µg kg-1 in spiked feather samples. The recoveries of azithromycin were 85.2-94.7% with the relative standard deviation less than 10%. The established method is simple, rapid, sensitive and specific, and could meet the need of government and enterprises to monitor the illegal use of azithromycin in livestock and poultry breeding.

Pipette-tip solid-phase extraction using cetyltrimethylammonium bromide enhanced molybdenum disulfide nanosheets as an efficient adsorbent for the extraction of sulfonamides in environmental water samples.

Surfactant cetyltrimethylammonium bromide enhanced molybdenum disulfide was used as an adsorbent in pipette-tip solid-phase extraction for the pretreatment of sulfonamides in environmental water samples. The factors affecting the extraction recoveries of the analytes, including the sample pH value, amount of sorbent, type and volume of eluent solution, and salt concentration were optimized. This pipette-tip solid-phase extraction method demonstrated good linearity (0.05-10.0 µg/L) with a coefficient of determination of 0.9984-0.9996, limit of detection (0.2-0.4 ng/L) and limit of quantitation (0.5-1.0 ng/L), good analyte recoveries (76-91), and acceptable limit of quantitation (<10%) under the optimized conditions. These results indicated that the proposed method was a good tool for monitoring sulfonamides in environmental water samples.

[Seasonal and Spatial Variations of Microcystins and Their Relationships with Physiochemical and Biological Factors in Poyang Lake].

Poyang Lake is the largest freshwater lake in China and an important drinking water source for Jiangxi Province. Since the year 2000, toxic cyanobacteria have been observed frequently in Poyang Lake. In this study, water samples were collected in the lake quarterly (April 2012, August 2012, October 2012, and January 2013) to examine the spatial and seasonal variations in the concentrations of microcystins (MCs; MC-RR, -YR, and -LR) and their relationships with physiochemical and biological factors. MCs were determined by ultra-high-performance liquid chromatography-electrospray ionization tandem triple quadrupole/mass spectrometry (UPLC-MS/MS). MC-RR (accounting for 75.01% and 71.34% of intracellular MC (IMC) and extracellular MC (EMC) concentrations, respectively) was the most dominant variant in Poyang Lake, followed by MC-LR (accounting for 21.95% and 24.97% of IMC and EMC concentrations, respectively), while MC-YR was detected in low concentrations (accounting for 3.01% and 3.69% of IMC and EMC concentrations, respectively). Total MC concentrations (IMC + EMC, TMC) ranged from 0.49 to 3517.85 ng·L-1, with an average of 337.43 ng·L-1 and only 2.53% (2 out of 79 water samples) of the water samples contained MCs concentrations exceeding the drinking water guideline level of 1 ng·L-1 for MC-LR proposed by World Health Organization (WHO). IMC concentrations showed significant relationships with Microcystis biomass (r=0.47, P<0.01), Oscillatoria biomass (r=0.68, P<0.01), Cyanobacteria biomass (r=0.56, P<0.01), and Chl-a (r=0.28, P<0.01), but no significant correlation was found between intracellular MC concentration and Anabena biomass (P>0.05), suggesting that Microcystis and Oscillatoria might be the main MCs-producing cyanobacteria in Poyang Lake. In addition, IMC concentrations were positively correlated with water temperature (r=0.51, P<0.01), transparence (r=0.69, P<0.01), Fe (r=0.43, P<0.01), and Zn contents (r=0.43, P<0.01), and negatively correlated with TN (r=-0.44, P<0.01), TP (r=-0.29, P<0.01), NH4+-N (r=-0.33, P<0.05), NO2--N (r=-0.28, P<0.05), Ca (r=-0.34, P<0.01), and Mg(r=-0.35, P<0.05), while no significant correlations were observed between IMC concentrations and pH, PO43--P, NO3--N, electrical conductivity, permanganate index, and Cu content (P>0.05). These results indicated that light intensity (represented by transparence), nitrogen, phosphorus, and water temperature might be the regulating factors of MCs production in Poyang Lake and trace elements (Fe, Zn, Ca, and Mg) can influence the MC production to a certain extent. IMCs and EMCs exhibited similar seasonal variations in Poyang Lake. The highest values of IMCs (531.87 ng·L-1) and EMCs (232.44 ng·L-1) were observed in summer. The concentrations of IMCs and EMCs in autumn were 31.97 ng·L-1 and 6.49 ng·L-1, respectively. Low concentrations were observed in spring (0.55 ng·L-1 and 0.88 ng·L-1 of IMCs and EMCs, respectively) and winter (0.69 ng·L-1 and 4.14 ng·L-1 of IMCs and EMCs, respectively). The highest IMCs and EMCs values of Poyang Lake in summer were 2298.08 ng·L-1 and 1219.77 ng·L-1, respectively, and the lowest values were 92.53 ng·L-1 and 38.80 ng·L-1, respectively. Overall, the concentrations of IMCs in eastern bays, the vicinity of Songmen Mountain, Banghu Lake, and its outlet were higher than those in other regions. However, the spatial distributions of EMCs in Poyang Lake were different from those of IMCs. EMCs concentrations in the vicinity of Songmen Mountain, Banghu Lake, and its outlet were higher than those in other regions.

Chitosan-poly(m-phenylenediamine)@Fe3O4 nanocomposite for magnetic solid-phase extraction of polychlorinated biphenyls from water samples.

A extraction medium based on chitosan-poly(m-phenylenediamine) (CS-PPD) @Fe3O4 nanocomposite was synthesized by chemical polymerization of m-phenylenediamine in the presence of chitosan coated magnetic nanocomposite, and for the first time, used as the sorbent for the magnetic solid-phase extraction (MSPE) of seven polychlorinated biphenyls (PCB28, PCB52, PCB101, PCB118, PCB138, PCB153, and PCB180) at trace levels in water samples. Gas chromatography-triple quadrupole mass spectrometry (GC-MS/MS) was used for PCBs quantification and detection. Several factors related to MSPE efficiencies, such as type and amount of sorbent, extraction time, sample pH, and desorption conditions were investigated. Under the optimized conditions, an excellent linearity was observed in the range of 1.0-200 ng L(-1) for PCB180, 0.5-200 ng L(-1) for the other six PCBs with the correlation coefficients ranging from 0.9954 to 0.9993. The good recoveries at spiked levels of 10.0, 20.0, and 50.0 ng L(-1) were obtained in the range of 94%-108%, and the coefficients of variations were less than 6%. The proposed method was feasible, rapid, and easy to operate for the trace analysis of the PCBs in local aquaculture water, livestock breeding water, and sewage water samples.

Ultrasound-assisted emulsification-microextraction for the sensitive determination of ethyl carbamate in alcoholic beverages.

A method based on ultrasound-assisted emulsification-microextraction (USAEME) was proposed in this contribution for the determination of ethyl carbamate (EC) in alcoholic beverages using gas chromatography coupled to triple quadrupole mass spectrometry. To achieve the determination of EC in alcoholic beverages, the influences on the extraction efficiency of type and volume of extraction solvent, temperature, ionic strength, alcohol content, and extraction time were studied, once the extraction solvent had been selected. The optimized conditions were 200.0 µL of chloroform at 30 °C during 5 min with 15% (m/v) sodium chloride addition. The detection limit, relative standard deviations, linear range, and recoveries under the optimized conditions were 0.03 µg L(-1), 4.2-6.1%, 0.1-50.0 µg L(-1), and 80.5-87.9%, respectively. Moreover, the feasibility of the present method was also validated by real samples. To the best of our knowledge, this is the first time that USAEME has been applied to determine a strongly hydrophilic compound in alcoholic beverages.

Applicability of accelerated solvent extraction for synthetic colorants analysis in meat products with ultrahigh performance liquid chromatography-photodiode array detection.

Accelerated solvent extraction (ASE) coupled with ultrahigh performance liquid chromatography (UHPLC) with photodiode array detection (PDA) has been used for the quantitative determination of synthetic colorants in meat products. Samples were extracted with ethanol-water-ammonia with a ratio of 75:24:1 (v/v/v) using ASE instrument at 85°C. As a result, all the colorants in meat products were separated using an optimized gradient elution within 3.5 min. Detection and quantification limits of synthetic colorants were in the ranges of 0.01-0.02 mg kg(-1) and 0.05 mg kg(-1), respectively. The intra-day and inter-day precision of the synthetic colorants were ranged between 1.7% (E123) to 5.2% (E124) and 3.2% (E124) to 6.0% (E129), respectively. The intra-day and inter-day recoveries of the synthetic colorants were ranged between 76.9% (E124) to 84.9% (E102) and 76.3% (E124) to 84.3% (E127), respectively. The method has been applied for the determination of seven synthetic colorants in meat products.

Non-covalent anionic porphyrin functionalized multi-walled carbon nanotubes as an optical probe for specific DNA detection.

With water-soluble anionic tetra (p-carboxyphenyl) porphyrin (TCPP) to solubilize multi-walled carbon nanotubes (MCNTs), we obtained a suspension that could be stable more than 1 week. With this TCPP/MCNTs suspension, we propose a spectrofluorometric method of DNA hybridization in this contribution. Our basic finding for this work is that the fluorescence from a dye-tagged single stranded DNA (ssDNA), which was directly added to the TCPP/MCNTs suspension, gets quenched, and the fluorescence could be remained if the dye-tagged single stranded DNA is first to be hybridized with its complementary target DNA to form a double stranded DNA (dsDNA) hybrid and added into the TCPP/MCNTs suspension. Mechanism investigations showed that the reason for the former is due to the adsorption of ssDNA on the surfaces of MCNTs, and that for the latter is due to the strong electrostatic repulsion force between the negative charge TCPP/MCNTs complexes and dsDNA. Thus, target DNA in a DNA sample and single-base mismatch in DNA sequences could be easily detected.

Conformational change detection of DNA with the fluorogenic reagent of o-phthalaldehyde-beta-mercaptoethanol.

o-Phthalaldehyde-beta-mercaptoethanol (OPAME) as a fluorogenic reagent has been found wide applications in the detection of amino acids based on its reaction with primary amino groups. In this contribution, we report our new findings concerning the reactions of OPAME with single-stranded DNA (ssDNA) and double-stranded DNA (dsDNA), respectively. It has been found that ssDNA can react with OPAME easily as a result of giving rise to strong fluorescence emissions, while dsDNA, prepared by hybridizing ssDNA with its complementary target prior to the reaction, displays inert chemical activity and gives out weak fluorescence emission. Mechanism investigations have shown that the reaction activity between OPAME and DNA depends on the amino groups that are related to the conformation of uncoiled and exposed extent of DNA structure, and thus the inert chemical activity of dsDNA results from screening of the dsDNA bases in the interior of the double strands. Therefore, we could design a way to detect conformation change of DNA with OPAME and further develop a novel, simple label-free sequence detection method for complementary and single-base mismatched ssDNA in the hybridization of DNA.

Telomere DNA conformation change induced aggregation of gold nanoparticles as detected by plasmon resonance light scattering technique.

It has been reported that adsorption of uncoiled DNA (u-DNA) on the surface of gold nanoparticles (Au-NPs) can prevent the nanoparticle suspensions from aggregation even if in salt medium. Herein we report that quadruplex DNA (q-DNA), which is formed from uncoiled telomere DNA, via intramolecular hydrogen bonds in the presence of potassium ion, cannot keep Au-NPs stable, and the q-DNA/Au-NPs coexisting suspensions display aggregation tendency, giving plasmon resonance light scattering (PRLS) signals of Au-NPs. Mechanism investigations through a single point energy calculation on u- and q-structures of telomere DNA showed that q-DNA, compared with u-DNA, has a much higher surface negative charge density, symmetrical charge distribution and well self-structural stabilization, could not be adsorbed on the surface of Au-NPs.

Light scattering sensing detection of pathogens based on the molecular recognition of immunoglobulin with cell wall-associated protein A.

In this contribution, we report a rapid optical detection method of pathogens using Staphylococcus aureus (S. aureus) as the model analyte based on the molecular recognition of immunoglobulin with cell wall-associated Protein A (SpA). It was found that the molecular recognition of human immunoglobulin (IgG) with protein A on the cell wall of S. aureus on glass slide sensing area could result in strong surface enhanced light scattering (SELS) signals, and the SELS intensity (deltaI) increases proportionally with the concentration of S. aureus over the range of 2.5x10(5)-1.0x10(8) CFU mL(-1) with right angle light scattering (RALS) signals detection mode. In order to identify the solid support based molecular recognition between IgG with SpA, we also employed water-soluble CdS quantum dots (CdS-QDs) as a fluorescent marker for IgG by immobilizing the IgG onto the surfaces of CdS-QDs through covalent binding in order to generate recognition probes for SpA on the cell wall of S. aureus. Consequently, the fluorescent method also showed that the detection for pathogens with solid supports is reliable based on the molecular recognition of IgG with SpA.

A light scattering and fluorescence emission coupled ratiometry using the interaction of functional CdS quantum dots with aminoglycoside antibiotics as a model system.

Any signals, if their intensities have simple functional relationship with analyte concentration, can be applied to analytical purposes. Rayleigh light scattering signals and fluorescence signals are twins in flurospectroscopy, so the light scattering signals are the major interference when the Stokes shift is small. Herein, we propose a light scattering and fluorescence emission (LS-FL) coupled ratiometry using CdS quantum dots (QDs) as a fluorescence probe to detect aminoglycoside antibiotics (AGs). As model analytes, AGs, when attached to the surface of CdS-QDs via electrostatic interaction in aqueous medium, result in strong enhanced light scattering (LS) emission characterized at 376nm and fluorescence quenching of CdS-QDs at 500nm. Thus, a ratiometry using the coexistent light scattering and fluorescent emission signals has been proposed. Based on the linear relationship between logarithm of light scattering and fluorescence emission ratio (R) and logarithm of AGs concentration, a novel assay of AGs is established with the limits of detection (3sigma) being 58-190nmol l(-1), and applied successfully to detect AGs injection and serum samples.