“…In situ growth is based on the immersion of the pretreated fiber in the reacting solution, allowing for the synthesis of the material directly onto its surface [7,[29][30][31][32]. In this context, stainless-steel (SS) supports are preferred to fused silica and quartz substrates, In situ growth (or deposition from solution), chemical vapor deposition (CVD), and atomic layer deposition (ALD) are the most commonly applied methodologies of in situ deposition.…”
“…The process is repeated until the desired coating provides a unique control on thin film formation in terms of conformal with atomic-level accuracy [29,34]. As for dual-stage deposition, different approaches have been pr physical adhesion, the sol-gel technique, and chemical cross-linking [7 The physical adhesion of a pre-synthesized material is the most procedure [7,[29][30][31][32]. Besides fiber pretreatment, the coating process steps: (i) the inert surface is immersed in an adhesive material (e.g., silic or epoxy glues) or pre-coated with a polymeric layer (usually polyac (ii) the fiber is dipped in the fine powdered supramolecular material with the intended thickness (multiple dipping cycles can be required) layer of adhesive material can be applied to increase the mechanical st and (iv) the fiber is dried and thermally conditioned to promote coati ing, and allowing for the evaporation of both the residual solvents and ucts.…”
“…Steps i-iii can be merged when the pretreated fiber is directly imm tion containing the suspended material without the need of an adhesiv In this case, the immersion-heating stages are usually performed mult the intended coating thickness. In physical adhesion, the adhesive (or t vent) used for developing the coating has a major impact on the SPM fecting the thermal and mechanical stability of the material, as well a As for dual-stage deposition, different approaches have been proposed, including physical adhesion, the sol-gel technique, and chemical cross-linking [7,29,30,32].…”
“…Steps i-iii can be merged when the pretreated fiber is directly immersed into a solution containing the suspended material without the need of an adhesive medium [29][30][31]. In this case, the immersion-heating stages are usually performed multiple times to obtain the intended coating thickness.…”
Solid-phase microextraction (SPME) has been widely proposed for the extraction, clean-up, and preconcentration of analytes of environmental concern. Enrichment capabilities, preconcentration efficiency, sample throughput, and selectivity in extracting target compounds greatly depend on the materials used as SPME coatings. Supramolecular materials have emerged as promising porous coatings to be used for the extraction of target compounds due to their unique selectivity, three-dimensional framework, flexible design, and possibility to promote the interaction between the analytes and the coating by means of multiple oriented functional groups. The present review will cover the state of the art of the last 5 years related to SPME coatings based on metal organic frameworks (MOFs), covalent organic frameworks (COFs), and supramolecular macrocycles used for environmental applications.
“…In situ growth is based on the immersion of the pretreated fiber in the reacting solution, allowing for the synthesis of the material directly onto its surface [7,[29][30][31][32]. In this context, stainless-steel (SS) supports are preferred to fused silica and quartz substrates, In situ growth (or deposition from solution), chemical vapor deposition (CVD), and atomic layer deposition (ALD) are the most commonly applied methodologies of in situ deposition.…”
“…The process is repeated until the desired coating provides a unique control on thin film formation in terms of conformal with atomic-level accuracy [29,34]. As for dual-stage deposition, different approaches have been pr physical adhesion, the sol-gel technique, and chemical cross-linking [7 The physical adhesion of a pre-synthesized material is the most procedure [7,[29][30][31][32]. Besides fiber pretreatment, the coating process steps: (i) the inert surface is immersed in an adhesive material (e.g., silic or epoxy glues) or pre-coated with a polymeric layer (usually polyac (ii) the fiber is dipped in the fine powdered supramolecular material with the intended thickness (multiple dipping cycles can be required) layer of adhesive material can be applied to increase the mechanical st and (iv) the fiber is dried and thermally conditioned to promote coati ing, and allowing for the evaporation of both the residual solvents and ucts.…”
“…Steps i-iii can be merged when the pretreated fiber is directly imm tion containing the suspended material without the need of an adhesiv In this case, the immersion-heating stages are usually performed mult the intended coating thickness. In physical adhesion, the adhesive (or t vent) used for developing the coating has a major impact on the SPM fecting the thermal and mechanical stability of the material, as well a As for dual-stage deposition, different approaches have been proposed, including physical adhesion, the sol-gel technique, and chemical cross-linking [7,29,30,32].…”
“…Steps i-iii can be merged when the pretreated fiber is directly immersed into a solution containing the suspended material without the need of an adhesive medium [29][30][31]. In this case, the immersion-heating stages are usually performed multiple times to obtain the intended coating thickness.…”
Solid-phase microextraction (SPME) has been widely proposed for the extraction, clean-up, and preconcentration of analytes of environmental concern. Enrichment capabilities, preconcentration efficiency, sample throughput, and selectivity in extracting target compounds greatly depend on the materials used as SPME coatings. Supramolecular materials have emerged as promising porous coatings to be used for the extraction of target compounds due to their unique selectivity, three-dimensional framework, flexible design, and possibility to promote the interaction between the analytes and the coating by means of multiple oriented functional groups. The present review will cover the state of the art of the last 5 years related to SPME coatings based on metal organic frameworks (MOFs), covalent organic frameworks (COFs), and supramolecular macrocycles used for environmental applications.
“…To overcome these problems, over time, miniaturized extraction methods have been developed for both the solid phase [ 18 ] and the liquid phase [ 19 ], with the aim of reducing the volume and toxicity of the extraction solvent and the amount of sample being processed to reduce the extraction time [ 20 ]. Due to the advantages offered, their applications are numerous [ 21 ], which is why we only mention their applicability to the analysis of steroids in urine [ 22 ] and in water [ 23 ]; of NSAIDs in water [ 24 ]; of steroids and NSAIDs in wastewater [ 25 ]; and, last but not least, in the analysis of steroids and NSAIDs in food samples [ 5 , 26 , 27 , 28 , 29 ].…”
This research aims to determine five steroids and four non-steroidal anti-inflammatory drugs in milk and egg samples collected from rural Roma communities in Transylvania, Romania. Target compounds were extracted from selected matrices by protein precipitation, followed by extract purification by dispersive liquid–liquid microextraction based on solidification of floating organic droplets. The extraction procedure was optimized using a 24 full factorial experimental design. Good enrichment factors (87.64–122.07 milk; 26.97–38.72 eggs), extraction recovery (74.49–103.76% milk; 75.64–108.60% eggs), and clean-up of the sample were obtained. The method detection limits were 0.74–1.77 µg/L for milk and 2.39–6.02 µg/kg for eggs, while the method quantification limits were 2.29–5.46 µg/L for milk and 7.38–18.65 µg/kg for eggs. The steroid concentration in milk samples was <MDL up to 4.30 µg/L, decreasing from 17α-ethinyl estradiol, 17β-estradiol, and estrone to estriol. The NSAID concentration was <MDL up to 3.41 µg/L, decreasing from ibuprofen, diclofenac, and ketoprofen to naproxen. The steroid concentration in the egg samples was <MDL to 2.79 µg/kg, with all steroids detected, while the concentration of NSAIDs was <MDL to 2.28 µg/kg, with only ibuprofen, ketoprofen, and naproxen detected. The developed protocol was successfully applied to the analysis of target compounds in real milk and egg samples.
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