Search

In the present study, a copper-based metal-organic framework (HKUST-1) was used first time for preconcentration trace amounts of addictive drugs in biological samples. HKUST-1 was synthesized and coated onto the surface of stainless steel wire. The prepared coating was used in headspace solid-phase microextraction method coupled with gas chromatography-mass spectrometry for preconcentration and determination of some addictive drugs in biological fluids. Prepared coating shows good extraction efficiency due to large surface area, and π-π stacking interaction with selected analytes. Under optimum conditions, the method was validated with a reasonable determination coefficient (R 2  > 0.9961) and suitable linear dynamic range (0.5-1000 μg L -1 ). Also, the limits of detections were obtained in the range of 0.1-0.4, 0.2-0.6, and 0.4-0.7 μg L -1 for water, urine, and plasma samples, respectively. The limits of quantification of present method were obtained in the range 0.5-1.3, 0.7-1.5, and 1.0-1.9 μg L -1 in water, urine, and plasma samples, respectively. The intra-day and inter-dye single fiber and fiber to fiber relative standard deviations were observed in the range 3.0-13.9% and 3.5-12.3%, respectively. Finally, the present method was applied for the determination of the drugs in biological samples., (© 2021 Wiley-VCH GmbH.)

This research is an application of fiber-in-tube solid-phase microextraction followed by high-performance liquid chromatography with UV detection for the extraction and determination of trace amounts of bisphenol A. Nanomagnetic Fe 3 O 4 was formed on the surface of polypropylene porous hollow fibers to increase the surface area and then it was coated with polystyrene. The introduction of polystyrene improves the surface hydrophobicity and is an appropriate extractive phase because it is highly stable in aquatic media. The extraction was carried out in a short capillary packed longitudinally with the fine fibers as the extraction medium. Extraction conditions, including extraction and desorption flow rates, extraction time, pH, and ionic strength of the sample solution, were investigated and optimized. Under optimal conditions, the limit of detection was 0.01 µg/L. This method showed good linearity for bisphenol A in the range of 0.033-1000 µg/L, with the coefficient of determination of 0.9984. The inter- and intraday precisions (RSD%, n = 3) were 7.9 and 6.3%, respectively. Finally, the method was applied to analysis of the analyte in thermal papers, disposable plastic cups, and soft drink bottles., (© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Porous frameworks are a term of attracting solid materials assembled by interconnection of molecules and ions. These trendy materials due to high chemical and thermal stability, well-defined pore size and structure, and high effective surface area gained attention to employ as extraction phase in sample pretreatment methods before analytical analysis. Solid-phase microextraction is an important subclass of sample preparation technique that up to now different configurations of this method have been introduced to get adaptable with different environments and analytical instruments. In this review, theoretical aspect and different modes of solid-phase microextraction method are investigated. Different classes of porous frameworks and their applications as extraction phase in the proposed microextraction method are evaluated. Types and features of supporting substrates and coating procedures of porous frameworks on them are reviewed. At the end, the prospective and the challenges ahead in this field are discussed., (© 2021 Wiley-VCH GmbH.)

A novel plate-like nano-sorbent based on copper/cobalt/chromium layered double hydroxide was synthesized by a simple coprecipitation method. The synthesized nanoparticels were introduced into a stainless steel cartridge using a dry packing method. Then, the packed cartridge was introduced as a novel on-line "packed in-tube" configuration and followed by high performance liquid chromatography for the determination of trace amounts of ∆ 9-tetrahydrocannabinol from biological samples and cannabis leaves. The as-prepared sorbent exhibited long lifetime, good chemical stability, and high anion-exchange capacity. Several important factors affecting the extraction efficiency, such as extraction and desorption times, pH of the sample solution and flow rates of the sample and eluent solutions, were investigated and optimized. Under optimized conditions, this method showed good linearity for ∆ 9-tetrahydrocannabinol in the ranges of 0.09-500, 0.3-500, and 0.4-500 µg/L with coefficients of determination of 0.9999, 0.9991, and 0.9994 in water, serum and plasma samples, respectively. The inter- and intra-assay precisions (n = 3) were respectively in the ranges of 1.8-4.6% and 1.9-4.0% at three concentration levels of 10, 50, and 100 µg/L. The limits of detection were also in the range of 0.02-0.1 µg/L., (© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

In this study, a novel 'fiber-in-tube' configuration was applied to electrochemically controlled fiber-in-tube solid-phase microextraction of antipsychotic drugs (perphenazine and chlorpromazine) from biological samples. To prepare an electrochemically controlled fiber-in-tube solid-phase microextraction column, first eight stainless-steel wires were placed into the stainless-steel column. Then, a nanostructured Cu-Cr-Al ternary layered double hydroxide/polythiophene coating was prepared on the inner surface of the stainless-steel tube and on the surfaces of the stainless-steel wires by a facile in situ electrodeposition method. The nanostructured coating exhibited enhanced long lifetime, good mechanical stability, high porosity, and large specific surface area compared with polythiophene and Cu-Cr-Al layered double hydroxide coatings. Under the optimal conditions, the limits of detection were in the range of 0.07-0.8 μg/L. This method showed good linearity for perphenazine and chlorpromazine in the ranges of 0.3-300 and 0.2-300 μg/L, respectively, with coefficients of determination more than 0.9982. The inter- and intra-assay precisions (RSD%, n = 3) were in the ranges of 3.0-5.1 and 2.5-4.5% at three concentration levels of 5, 25 and 50 μg/L, respectively. Finally, the method was applied for the analysis of the drugs in human urine and plasma samples., (© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)