A high-throughput and environmentally friendly method based on 96-well plate thin-film microextraction was established to determine 14 fungicides in grapes and grape juice using liquid chromatography-tandem mass spectrometry. The thin-film microextraction optimized method consisted of 60 min of extraction at pH 6.0 with the addition of sodium chloride (2-5%). Acetonitrile/water in the ratio of 8:2 was used for desorption analytes for 60 min. Evaluation of different extractive phases showed that polyacrylonitrile-polystyrene-divinylbenzene was the optimum coating. The linearity of the method was good in the range of 0.01-0.5 μg/mL for 14 fungicides with determination coefficients (R ) from 0.990 to 0.999, which indicated good linearity for both the grape juice and grape matrixes. The limit of detection was in the range of 0.002-0.01 μg/mL. The limit of quantitation was in the range of 0.01 mg/kg according to the minimum fortified level. The average absolute recoveries of the 14 fungicides ranged from 75.0 to 118.3%. The intraday relative standard deviation (n = 4) and interday relative standard deviation (n = 4) were 5.6-13.0% and 1.6-6.4%, respectively. This study showed that this method can be used for analyzing 96 samples in parallel, and the sample preparation time was approximately 2.0 min per sample. In addition, this approach offers a green and low-cost sample pretreatment technique for future analyses.
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http://dx.doi.org/10.1002/jssc.201900900 | DOI Listing |
J Chromatogr A
December 2024
Electroanalytical Chemistry Research Laboratory, Department of Analytical Chemistry, Faculty of Chemistry, University of Mazandaran, Babolsar, Iran.
A new thin film was fabricated using FeO@SiO-polyoxometalate (POM) as the coating and it was coupled with a HPLC-UV to develop a method for the selective determination of ibuprofen, paracetamol and diclofenac (as the model analytes) from human plasma and urine samples. The prepared magnetic POM was coated on the pores and surface of cotton yarn to prepare the extracting device. The prepared sorbent was characterized by several techniques including: FT-IR, XRD, BET, SEM, and VSM analysis.
View Article and Find Full Text PDFAnal Chim Acta
January 2025
Environmental and Bio-Analytical Laboratories, Department of Chemistry, Sharif University of Technology, P.O. Box 11365-9516, Tehran, Iran. Electronic address:
Background: Periodic mesoporous organosilicas (PMOs) are a new class of organic-inorganic hybrid materials with high surface area, narrow pore size distribution, high functional group loading, and tunable functional groups. In contrast to other porous organosilicate materials, PMOs show a uniform distribution of organic groups inside their framework walls. They are synthesized by condensing bis-silylated organic precursors around a surfactant template.
View Article and Find Full Text PDFAnal Chim Acta
January 2025
MOE Key Laboratory of Bioinorganic and Synthetic Chemistry/KLGHEI of Environment and Energy Chemsistry, School of Chemistry, Sun Yat-sen University, Guangzhou, 510006, PR China.
Fast and accurate determination of persistent organic pollutants (POPs) plays a crucial role in addressing concerns related to public security and environmental safety. Herein, a unique thin film based solid phase microextraction (denoted as TF-SPME) method was reported and used for on-site analysis of POPs via loading the TFs into a homemade sampling device and equipped on a drone, which can load up to 6 pieces of TFs at the same time. The parallel 6 pieces of TFs offered significant advantages in terms of efficiency, accuracy, cost-effectiveness and comparability of sampling.
View Article and Find Full Text PDFJ Sep Sci
December 2024
College of Chemistry, Tianjin Key Laboratory of Biosensing and Molecular Recognition, Nankai University, Tianjin, China.
In this work, the covalent organic frameworks-incorporated electrospun nanofiber membranes were used as a highly efficient adsorbent to enrich quinolone antibiotics in food samples. Covalent organic frameworks composed of 1,3,5-tris(4-aminophenyl) benzene and 2,5-dihydroxyterephthalaldehyde were rapid prepared only 20 min at room temperature, then were further synthesized into electrospun polyacrylonitrile nanofiber membranes by electrospinning the binary precursors solution directly. Coupled with high-performance liquid chromatography with ultraviolet detector, the method exhibited good linearity in the range of 1-100 ng·mL for four quinolone antibiotics, with low limits of detection 0.
View Article and Find Full Text PDFAnal Chim Acta
December 2024
Grupo de Investigación en Cromatografía y Técnicas Afines GICTA, Departamento de Química, Facultad de Ciencias Exactas y Naturales, Universidad de Caldas, Calle 65 # 26-10, Manizales, 170004, Colombia. Electronic address:
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