Effective extraction of fluoroquinolones from water using facile modified plant fibers.

In this study, ecofriendly and economic carboxy-terminated plant fibers (PFs) were used as adsorbents for the effective in-syringe solid phase extraction (IS-SPE) of fluoroquinolone (FQ) residues from water. Based on the thermal esterification and etherification reaction of cellulose hydroxy with citric acid (CA) and sodium chloroacetate in aqueous solutions, carboxy groups grafted onto cotton, cattail, and corncob fibers were fabricated. Compared with carboxy-terminated corncob and cotton, CA-modified cattail with more carboxy groups showed excellent adsorption capacity for FQs. The modified cattail fibers were reproducible and reusable with relative standard deviations of 3.2%-4.2% within 10 cycles of adsorption-desorption. A good extraction efficiency of 71.3%-80.9% was achieved after optimizing the extraction condition. Based on carboxylated cattail, IS-SPE coupled with ultra-performance liquid chromatography with a photodiode array detector was conducted to analyze FQs in environmental water samples. High sensitivity with limit of detections of 0.08-0.25 µg/L and good accuracy with recoveries of 83.8%-111.7% were obtained. Overall, the simple and environment-friendly modified waste PFs have potential applications in the effective extraction and detection of FQs in natural waters.

One-step fabrication of COF-coated melamine sponge for in-syringe solid-phase extraction of active ingredients from traditional Chinese medicine in serum samples.

In this study, a covalent organic framework (COF)-TpBD-supported melamine sponge (MS) was fabricated through a one-step hydrothermal method. The obtained monolithic column was then applied in in-syringe solid-phase extraction (IS-SPE) for the separation of three volatile ingredients from serum samples. Given credit for the superior adsorption capacity of the COF and the homogeneous microporous property of MS, the developed column exhibited satisfactory separation of the targets. And the dominating adsorption mechanism was the hydrophobic interaction forces between TpBD and targets and the high mass transfer efficiency provided by the large pore structure of MS. The results of dynamic adsorption showed that the MS@TpBD column displayed much better adsorption performance than blank MS and TpBD. And it has featured great reusability up to 5 cycles and obtained satisfied recovery values (87.9 ~ 110.3%) in serum samples. As a result of sample clean-up, this column offers low limit of detections (LODs) down to 0.014, 0.010, and 0.020 µg/mL, respectively. In summary, we believe that this convenient separation column has prominent application promise in the fields of separating activity ingredients in biological samples.

Ferric iron loaded porphyrinic zirconium MOFs on corncob for the enhancement of diuretics extraction.

Herein, corncob waste was used as a scaffold for the fabrication of effective adsorbents. Porphyrinic zirconium metal-organic frameworks (MOFs) PCN-223 and PCN-224 constructed by different numbers of Zr6 cluster nodes were grown on the surface of the corncob. Fe (Ш) ions were implanted in the porphyrin ring by post-synthesis modification. The results showed that the extraction capacity of diuretics on PCN-224@corncob containing suitable pore size was larger than that of PCN-223@corncob. The adsorption of diuretics was further enhanced because of the electrostatic effect caused by implantation of Fe (Ш) ions. PCN-224-Fe@corncob was recyclable and selective for the extraction of furosemide (Fur) and bumetanide (Bum). Coupled in-syringe solid phase extraction (IS-SPE) with ultra-performance liquid chromatography (UPLC), an efficient, sensitive, and stable method was established. With a sensitivity between 0.6 and 1.0 µg/L and a recovery between 83.2% and 119.2%, it is used for the analysis of trace amounts of Fur and Bum in weight loss products and environmental water. The functionalized corncob has potential application for the adsorption of diuretics, and the metal ions implantation in MOFs provides a promising strategy for enhancing extraction capacity.

In-syringe solid phase extraction and in-syringe vortex-assisted solidified floating organic drop microextraction of Sb(III) and Sb(V) in rice wines with determination by graphite furnace atomic absorption spectrometry.

The current non-chromatographic speciation methods generally involve the conversion of different species by oxidation/reduction reactions, which may cause inherent problems such as contamination risk, time consumption and complex operations. In this work, in-syringe solid phase extraction (IS-SPE) was combined with in-syringe vortex-assisted solidified floating organic drop microextraction (IS-VA-SFODME) for the detection of Sb(V) and Sb(III) in rice wines by graphite furnace atomic absorption spectrometry. Firstly, IS-SPE involved the use of ZnFe2O4 nanotubes as the sorbent for the isolation and enrichment of Sb(V) and removal of the matrix components such as ethanol, pigment, sugars and carbohydrates. Then, IS-VA-SFODME was used for enriching Sb(III) in the original sample solution after IS-SPE. This technique exhibited good anti-interference ability and high enrichment efficiency without tedious pre-oxidation/pre-reduction and centrifugation/filtration operations, which may cause the contamination of samples. Under the selected conditions, the detection limits were 4.5 ng L-1 and 3.2 ng L-1 for Sb(III) and Sb(V) with relative standard deviations of 7.3% and 5.1%, respectively. This procedure was used with satisfactory results for the detection of Sb(III) and Sb(V) in rice wine samples and a certified reference material of water sample. Recoveries of spiked experiments ranged from 91.0 to 107%.

Effective extraction of fluoroquinolones from water using facile modified plant fibers / 药物分析学报

In this study,ecofriendly and economic carboxy-terminated plant fibers(PFs)were used as adsorbents for the effective in-syringe solid phase extraction(IS-SPE)of fluoroquinolone(FQ)residues from water.Based on the thermal esterification and etherification reaction of cellulose hydroxy with citric acid(CA)and sodium chloroacetate in aqueous solutions,carboxy groups grafted onto cotton,cattail,and corncob fibers were fabricated.Compared with carboxy-terminated corncob and cotton,CA-modified cattail with more carboxy groups showed excellent adsorption capacity for FQs.The modified cattail fibers were reproducible and reusable with relative standard deviations of 3.2％-4.2％within 10 cycles of adsorption-desorption.A good extraction efficiency of 71.3％-80.9％was achieved after optimizing the extraction condition.Based on carboxylated cattail,IS-SPE coupled with ultra-performance liquid chromatography with a photodiode array detector was conducted to analyze FQs in environmental water samples.High sensitivity with limit of detections of 0.08-0.25 μg/L and good accuracy with recoveries of 83.8％—111.7％were obtained.Overall,the simple and environment-friendly modified waste PFs have potential appli-cations in the effective extraction and detection of FQs in natural waters.

Rapid detection of sulfamethoxazole in plasma and food samples with in-syringe membrane SPE coupled with solid-phase fluorescence spectrometry.

In this work, in-syringe membrane solid-phase extraction (MSPE) device was fabricated for the on-site sampling of sulfamethoxazole (SMX) in food samples followed by solid-phase fluorescence spectra analysis. The samples and fluorescamine (FA) were added to a syringe for derivation. Then, the derivative of SMX was extracted by a membrane in the syringe SPE device. Subsequently, the derivative on the membrane was measured immediately without additional elution procedure. The method was successfully applied in plasma, milk, and egg samples for the trace SMX detection, with the recovery of 98%-102%, RSDs from 1% to 6%. Compared with liquid chromatography, direct detection of the concentrated analyte significantly improved the sensitivity. Moreover, fluorescamine made it unnecessary to separate SMX from the interference. Consequently, it was a time-saving, low-cost, and easy-operation method, which demonstrated the potential of in-syringe SPE as a promising candidate for on-site analysis.

Electrospun polymer composite nanofiber-based in-syringe solid phase extraction in tandem with dispersive liquid-liquid microextraction coupled with HPLC-FD for determination of aflatoxins in soybean.

A fast method based on in-syringe solid phase extraction combined with dispersive liquid-liquid microextraction was developed for extraction of aflatoxins prior to HPLC-FD. Electrospun polyurethane nanofibers doped with graphene oxide were collected on a thin metal net sheet without using a binder, placed into a filter holder between filter papers on a syringe tip and used as an efficient adsorbent for the first time. The major parameters affecting whole extraction efficiency were investigated and optimized. Under the optimum conditions, the limits of detection and the limits of quantification were in the range of 0.09-0.15 and 0.3-0.5 µg kg-1, respectively. The linear dynamic range was 0.3-1000 µg kg-1 with determination coefficients of 0.9946-0.9965. The inter- and intra-day precisions were lower than 4.3 and 7.2%, respectively. The method was successfully applied for the determination of aflatoxins B1, B2, G1, and G2 in soybeans and satisfactory relative recoveries of 76-101% were achieved.

Self-assembling covalent organic framework functionalized poly (styrene-divinyl benzene-glycidylmethacrylate) composite for the rapid extraction of non-steroidal anti-inflammatory drugs in wastewater.

The growing use of non-steroidal anti-inflammatory drugs (NSAIDs) has seriously affected human health and ecosystems, as a result, the World Health Organization (WHO) has regarded them as emerging contaminants. NSAID's polar nature and trace amount present in wastewater make their extraction and determination challenging in modern analytical science. Therefore, regarding the need, we herein report a rapid, sensitive and selective in-syringe solid-phase extraction (SPE) method coupled with ultrahigh performance liquid chromatography and UV detector for the determination of seven NSAIDs in environmental water samples. Specifically, the NSAIDs in water samples were directly extracted by using synthesized porous covalent organic framework functionalized poly (styrene-divinyl benzene-glycidylmethacrylate) composite (COF@PS-GMA) without further cleanup procedures. The adsorption of NSAIDs on COF@PS-GMA sorbent was investigated by using adsorption isotherms and kinetic studies. Various parameters, including amount of sorbent, pH of the samples, the volume of desorption solvent, and desorption time that were involved in in-syringe SPE were optimized. Under the optimized conditions, good linearity was observed at 0.005-5.0 µg mL-1 with method quantification limits (LOQs) estimated between 0.54-2.74 µg L-1. The recoveries of the seven NSAIDs at the level of 0.5, 5.0 and 20.0 µg L-1 were ranging from 84.3% to 99.6%.

In-syringe solid-phase extraction for on-site sampling of pyrethroids in environmental water samples.

On-site sampling is an analytical approach that can ensure the accuracy of monitoring data and enhance the effectiveness of environmental protection measures. In the present work, an in-syringe solid-phase extraction (SPE) device was designed for on-site sampling of trace contaminants in environmental water samples followed by gas chromatography-mass spectrometry (GC-MS) analysis. Template assisted freeze casting followed by hydrazine vapor reduction approach was used to synthesize a hierarchical porous graphene aerogel (HPGA), which was used as the sorbent in the in-syringe SPE device. Environmental degradable pyrethroids were selected as the model analytes. Owing to the large specific surface area and hydrophobicity of HPGA, the target molecules could be completely extracted during one aspirating/dispensing cycle. The analytes were stable on the sorbent for at least 72 h when the device was stored under airtight and light-free conditions, and were not affected by the pH value of sample solution. All results demonstrated that the device could meet the requirements of on-site sampling. For practical application, the limits of detection were found to be in the range of 0.012-0.11 ng mL-1 under the optimized conditions, and satisfactory recoveries in the range of 65.7-105.9% were obtained for the analysis of real samples. The results of this study demonstrate the immense potential of HPGA for the enrichment of trace environmental pollutants, and meanwhile promote the application of the in-syringe SPE technique as a promising candidate for on-site sampling.

Metal-organic framework based in-syringe solid-phase extraction for the on-site sampling of polycyclic aromatic hydrocarbons from environmental water samples.

In-syringe solid-phase extraction is a promising sample pretreatment method for the on-site sampling of water samples because of its outstanding advantages of portability, simple operation, short extraction time, and low cost. In this work, a novel in-syringe solid-phase extraction device using metal-organic frameworks as the adsorbent was fabricated for the on-site sampling of polycyclic aromatic hydrocarbons from environmental waters. Trace polycyclic aromatic hydrocarbons were effectively extracted through the self-made device followed by gas chromatography with mass spectrometry analysis. Owing to the excellent adsorption performance of metal-organic frameworks, the analytes could be completely adsorbed during one adsorption cycle, thus effectively shortening the extraction time. Moreover, the adsorbed analytes could remain stable on the device for at least 7 days, revealing the potential of the self-made device for on-site sampling of degradable compounds in remote regions. The limit of detection ranged from 0.20 to 1.9 ng/L under the optimum conditions. Satisfactory recoveries varying from 84.4 to 104.5% and relative standard deviations below 9.7% were obtained in real samples analysis. The results of this study promote the application of metal-organic frameworks in sample preparation and demonstrate the great potential of in-syringe solid-phase extraction for the on-site sampling of trace contaminants in environmental waters.