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1.
Anal Methods ; 15(29): 3510-3521, 2023 07 27.
Article in English | MEDLINE | ID: mdl-37434587

ABSTRACT

This study assessed the use of magnetic biosorbents in dispersive solid-phase extraction with a gas chromatograph-electron capture detector for the determination of trifluralin, chlorothalonil, transfluthrin, bromopropylate, and bifenthrin in water samples. To our knowledge, this is the first time that magnetic cork composites are used as an adsorbent in dispersive solid-phase extraction. The advantages of magnetic cork composites include their density regulation and high surface areas. The magnetic composites can be recovered using a magnetic field for desorption purposes, which can improve the operation process and reduce the extraction time. Moreover, the parameters affecting the extraction performances were optimized. The method has a limit of detection between 0.30 and 2.02 µg L-1. Good linearities (R2 > 0.99) were obtained in the linear range of 1.00 to 2000 µg L-1. The relative recoveries of the analytes in tap water, river, and lake water samples spiked at different concentrations ranged between 90% and 104%, and the relative standard deviations were less than 7.1%. Therefore, this study showed that Fe3O4/cork magnetic composites can be used as efficient and eco-friendly biosorbents in dispersive solid-phase extraction for the determination of pesticides in water samples. The use of these composites contributes to the current trend of green chemistry.


Subject(s)
Pesticides , Pesticides/analysis , Solid Phase Extraction/methods , Water , Magnetics , Magnetic Phenomena
2.
Molecules ; 29(1)2023 Dec 20.
Article in English | MEDLINE | ID: mdl-38202628

ABSTRACT

In recent years, the utilization of biomass materials for the removal and detection of water pollutants has garnered considerable attention. This study introduces, for the first time, the preparation of Fe3O4/persimmon leaf magnetic biomass composites. The magnetic composites were employed in a magnetic solid-phase extraction method, coupled with gas chromatography-electron capture detection (GC-ECD), for the analysis of four pesticides (trifluralin, triadimefon, permethrin, and fenvalerate) in environmental water samples. The innovative magnetic persimmon leaf composites were synthesized by in situ generation of Fe3O4 nanoparticles through coprecipitation and loaded onto persimmon leaves. These composites exhibit superparamagnetism with a saturation magnetization of 12.8 emu g-1, facilitating rapid phase separation using a magnetic field and reducing the extraction time to 10 min. Desorption can be achieved within 30 s by aspirating 20 times, eliminating the need for time-consuming and labor-intensive experimental steps like filtration and centrifugation. The specific surface area of the magnetic composite adsorbent increased from 1.3279 m2 g-1 for the original persimmon leaf to 5.4688 m2 g-1. The abundant hydroxyl and carboxyl groups on the composites provide ample adsorption sites, resulting in adsorption capacities ranging from 55.056 mg g-1 to 73.095 mg g-1 for the studied pesticides. The composites exhibited extraction recoveries ranging from 80% to 90% for the studied pesticides. Compared to certain previously reported MSPE methods, this approach achieves equivalent or higher extraction recoveries in a shorter operation time, demonstrating enhanced efficiency and convenience. Good linearity of the target analytes was obtained within the range of 0.75-1500 µg L-1, with a determination of coefficient (R2) greater than 0.999. These findings contribute to the use of magnetic persimmon leaf biomass materials as effective and environmentally friendly adsorbents for pollutant determination in water samples.


Subject(s)
Diospyros , Pesticides , Physical Phenomena , Electrons , Water
3.
J Chromatogr A ; 1675: 463136, 2022 Jul 19.
Article in English | MEDLINE | ID: mdl-35613507

ABSTRACT

Chemical protection is one of the most important methods to control forest pests. Since pesticides used in chemical protection might have significant adverse effects on aquatic organisms, it is essential to monitor and detect trace pesticides in environmental water. In this study, an on-site natural deep eutectic solvent-based multiple air-assisted liquid-liquid microextraction coupled with gas chromatography-electron capture detection was developed for determining triadimefon, bifenthrin, bromopropylate, and permethrin in water samples in the forest. A series of menthol-based deep eutectic solvents were synthesized for the first time to find green and efficient extractants. Moreover, a deep eutectic solvent with a 1:2 molar ratio of DL-menthol to citric acid was selected as the extractant due to its high stability and extraction performance. A portable modular array device based on air-assisted liquid-liquid microextraction was designed and manufactured to enable the simultaneous pretreatment of several samples. Although no electric equipment is required throughout the process, up to six samples were pretreated on-site within 20 min. Moreover, the average sample pretreatment time was less than 3.5 min, and the process was substantially simplified and enhanced. In addition, the parameters affecting the extraction performance were optimized. The extraction recoveries were in the range of 92-95% by using the optimized conditions, and the relative standard deviations of the intra-device, inter-device, intra-day, and inter-day factors were all less than 4.9%. The detection limits of the method ranged from 0.34 to 3.3 µg L-1. Good linearities (R2>0.999) were shown in the linear range of 1.13 to 2500 µg L-1 for the studied pesticides. Moreover, the proposed method was proved to be highly environmentally friendly by the Analytical Eco-Scale and Green Analytical Procedure Index. In summary, the proposed method is green, efficient, and flexible for on-site water sample pretreatment. The fact that tedious operations can be converted into standard operations provides a new perspective for on-site sample processing.


Subject(s)
Liquid Phase Microextraction , Pesticides , Deep Eutectic Solvents , Limit of Detection , Liquid Phase Microextraction/methods , Menthol , Solvents/chemistry , Water/chemistry
4.
J Sep Sci ; 45(6): 1252-1261, 2022 Mar.
Article in English | MEDLINE | ID: mdl-35001514

ABSTRACT

In this study, switchable hydrophilic solvent-based dispersive liquid-liquid microextraction coupled with high-performance liquid chromatography was developed for the determination of four sulfonylurea herbicides in soils. For the first time, the sample pretreatment was achieved due to the similar acid-base status of sulfonylurea herbicides and switchable hydrophilic solvent. In the extraction step, sulfonylurea herbicides were extracted as anions and transferred to an alkaline solution with switchable hydrophilic solvent anions. In the concentration step, two types of anions were transformed to their molecular state after the aqueous solution was acidified. In addition, the dispersion and microextraction processes were completed efficiently with the simultaneous formation of analytes and extractants. The factors affecting the extraction performance were optimized. Under the optimized conditions, good linearity was observed for each herbicide with correlation coefficients ranging from 0.9952 to 0.9978. The limits of detection were in the range of 0.1-0.2 µg/g. Moreover, the relative recoveries of the sulfonylurea herbicides at spiking levels of 0.5, 1, and 1.5 µg/g in soil samples were between 75 and 111% (relative standard deviations: 0.4-11.4%). Therefore, the proposed method in this study could be successfully applied to the analysis of four types of sulfonylurea herbicides in soil samples.

5.
In Vitro Cell Dev Biol Anim ; 56(7): 550-558, 2020 Aug.
Article in English | MEDLINE | ID: mdl-32886291

ABSTRACT

MiR-183 is a tumor onco-miR and has been shown by our previous studies to be overexpressed in esophageal squamous cell carcinomas (ESCCs). In this study, we sought to determine the possible mechanisms of miR-183 in ESCC. In our study, cell migration and invasion, real-time PCR, Western blot, and chromatin immunoprecipitation (ChIP) assays were used to explore the mechanism of miR-183 in three ESCC cell lines. We found several potential transcription factors, including c-Jun, by bioinformatics methods. Using a ChIP assay, we identified that c-Jun binds to the promoter region of pre-miR-183 and that upregulated c-Jun expression is related to increased expression of miR-183. We found that downregulation of miR-183 significantly reduced the cell invasiveness and migration of ESCC cells, whereas upregulation of miR-183 via a mimic increased the cell migration and invasion of ESCC cells. We further discovered one direct miR-183 target gene, Smad4, which has been implicated in invasion and metastasis. Furthermore, miR-183 promoted epithelial-mesenchymal transition (EMT), which is involved in the invasion and migration of ESCC cells. Dysregulation of miR-183 has an important role in tumor growth and invasion because miR-183 targets Smad4. Therefore, suppression of miR-183 may provide a potential approach for treatment.


Subject(s)
Esophageal Neoplasms/genetics , Esophageal Neoplasms/pathology , Esophageal Squamous Cell Carcinoma/genetics , Esophageal Squamous Cell Carcinoma/pathology , MicroRNAs/genetics , Proto-Oncogene Proteins c-jun/metabolism , Smad4 Protein/genetics , Up-Regulation/genetics , Cell Line, Tumor , Cell Movement/genetics , Cell Proliferation/genetics , Epithelial-Mesenchymal Transition/drug effects , Epithelial-Mesenchymal Transition/genetics , Gene Expression Regulation, Neoplastic/drug effects , Humans , MicroRNAs/metabolism , Models, Biological , Neoplasm Invasiveness , Smad4 Protein/metabolism , Transforming Growth Factor beta1/pharmacology
6.
J Speech Lang Hear Res ; 57(4): 1548-63, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24686556

ABSTRACT

PURPOSE: This article reports on the development of a self-report tool-the Chinese Hearing Aid Outcomes Questionnaire (CHAOQ)-to evaluate hearing aid outcomes among Chinese speakers. METHOD: There were 4 phases to construct the CHAOQ and evaluate its psychometric properties. First, items were selected to evaluate a range of culturally relevant outcomes. These procedures provided evidence for face and content validity. Second, items with inappropriate psychometric properties were eliminated. Items related to listening performance were subjected to exploratory factor analysis to identify the factor structure, which was later confirmed via a confirmatory factor analysis in Phase III. These procedures also ensured content and discriminant validity. Internal consistency reliability was evaluated, and normative data were obtained. Finally, test-retest reliability was evaluated, and construct validity was established by comparing results with corresponding items from the International Outcome Inventory for Hearing Aids. RESULTS: The final 26-item CHAOQ contains (a) 3 scales evaluating speech understanding in situations in which communication is relatively more difficult or easy or includes reduced listening cues; (b) a scale evaluating listening comfort; (c) a scale measuring negative responses; and (d) an item measuring overall satisfaction. CONCLUSION: The CHAOQ possesses good reliability and validity.


Subject(s)
Correction of Hearing Impairment/psychology , Hearing Aids/psychology , Hearing Loss/psychology , Self Report/standards , Adult , Aged , China , Correction of Hearing Impairment/methods , Female , Hearing Loss/rehabilitation , Humans , Language , Male , Middle Aged , Patient Comfort , Patient Satisfaction , Psychometrics , Reproducibility of Results , Speech Perception , Treatment Outcome , Young Adult
7.
Acta Crystallogr Sect E Struct Rep Online ; 68(Pt 12): o3254, 2012 Dec 01.
Article in English | MEDLINE | ID: mdl-23468773

ABSTRACT

The title compound, C12H14N2O, was obtained by reaction of (±)-1-(1H-benzimidazol-2-yl)ethanol with 3-bromo-prop-1-ene. The asymmetric unit contains four crystallographically independent mol-ecules. In the crystal, mol-ecules 1 and 2 are linked via O-H⋯N hydrogen bonds, forming chains propagating along [010]. Molecules 3 and 4 are linked to these chains via O-H⋯O hydrogen bonds.

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