Magnetic Dispersive Solid-phase Extraction Research Articles

Speciation of trace amounts of Sb(III) and Sb(V) in environmental water using inductively coupled plasma mass spectrometry after magnetic solid-phase extraction with rGO/Fe3O4.

We developed an approach of magnetic dispersive solid-phase extraction (MSPE) based on magnetic graphene nanocomposite rGO/Fe3O4 for the determination of trace Sb(III) and Sb(V) using inductively coupled plasma mass spectrometry (ICP-MS). Scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FT-IR) were used to characterize the sorbent. The adsorption behavior of Sb(III) and Sb(V) on rGO/Fe3O4 was investigated. The results showed that the adsorption capacity of Sb(V) was nearly zero at pH = 9, while Sb(III) could be well adsorbed on rGO/Fe3O4. The magnetic SPE parameters including pH, adsorbent dosage, eluent type, and volume were optimized. The detection limit of Sb(III) under ideal conditions was 6 ng L-1, and the relative standard deviation was 7.6% (c = 1 g L-1, n = 7). The technique was used to identify Sb(III) at trace levels in environmental water samples, and its validity was examined by recovery experiments and the examination of an approved reference material.

Development of a Novel Sensitive and Fast Semi-Covalent Molecularly Imprinted Polymer-Based Magnetic Dispersive Solid-Phase Extraction Method (MIP-MDSPE) for Cholesterol Determination in Milk Samples

In the present study, a novel magnetic dispersive solid-phase extraction method using molecularly imprinted polymer synthesized through semi-covalent imprinting approach was developed for cholesterol (CHO) determination in milk samples by high-performance liquid chromatography with diode array detector (HPLC-DAD). The adsorbent named Fe3O4/SiO2/MIP (MIP: molecularly imprinted polymers) was prepared through sol-gel polymerization of 3-(triethoxysilyl)propyl isocyanate (ICPTES) covalently bonded to CHO with tetraethoxysilane (TEOS), in the presence of Fe3O4/SiO2 particles. The adsorbent was characterized by attenuated total reflection Fourier transform infrared (ATR-FTIR), X-ray diffraction (XRD), dynamic light scattering (DLS) and scanning electron microscopy (SEM). The proposed molecularly imprinted polymer-based magnetic dispersive solid-phase extraction method (MIP-MDSPE) was based on vortex-assisted preconcentration of 10.0 mL of CHO solution in chloroform as donor phase using 10.0 mg of Fe3O4/SiO2/MIP during 60 s. After this step, the magnetic particles were collected using a permanent magnet and the vortex-assisted elution was carried with 500 µL of ethanol during 180 s. A wide analytical curve ranging from 38.5 to 25000 µg L-1 (determination coefficient (R2 ) = 0.998) and low limits of detection (LOD) and quantification (LOQ) 11.5 and 38.5 µg L-1, respectively, were obtained. Milk samples (whole and reduced-fat milk) were subjected to MIP-MDSPE method after saponification reaction followed by CHO extraction with chloroform. Using external calibration, the CHO concentration ranged from 99.2 (reduced-fat milk) to 397.6 mg kg-1 (whole milk) and the accuracy was attested by addition and recovery tests (92 to 97%).

Magnetic dispersive solid-phase extraction of some pesticides from fruit juices using monodisperse nanosorbent combined with dispersive liquid-liquid micro-extraction.

In this study, the new synthesized magnetic nanoparticles based on amorphous carbon have been used as a sorbent in magnetic dispersive solid-phase extraction prior to dispersive liquid-liquid micro-extraction. The developed method was applied for analysis of ten pesticides from different fruit juice samples by gas chromatography-flame ionization detection. In this work, a few mg of the sorbent is added into an aqueous solution containing the analytes. Adsorption and desorption of the compounds of interest are accelerated by vortexing and sonication, respectively. To achieve high enrichment factors, a suitable organic solvent (iso-propanol) is used to elute the target analytes from the nanosorbent. The obtained iso-propanol is phased and 1,1,2-trichloroethane are employed as the disperser and extraction solvents, respectively, in the following micro-extraction procedure. The synthesized magnetic nanoparticles were characterized by scanning electron microscope, X-ray diffraction, vibrating sample magnetometer, and Fourier-transform infrared spectrophotometer. To achieve the high extraction efficiency and optimum conditions, all parameters that could affect the extraction yield were investigated. Under optimum conditions, the method had broad linear ranges with a proper linearity (r2 ≥ 0.9987). Limits of detection and quantification for analysis of the selected pesticides were found in the ranges of 0.5-1.0 and 1.7-3.3µg L-1, respectively. High enrichment factors and extraction recoveries were obtained in the ranges of 321-438 and 64-88%, respectively. To evaluate repeatability of the method, it was performed on two sets of standard solutions at the concentrations of 10 and 50µg L-1 (each analyte). Relative standard deviations varied in the ranges of 2-6% and 4-7% for intra- (n = 6) and inter-day (n = 5) precisions, respectively.

Direct magnetic sorbent sampling flame atomic absorption spectrometry (DMSS-FAAS) for highly sensitive determination of trace metals

A procedure of direct magnetic sorbent sampling in flame atomic absorption spectrometry (DMSS-FAAS) was developed in this work. Metal-loaded magnetic sorbents were directly inserted in the flame of the FAAS for direct metal desorption/atomization. Magnetic graphene oxide aerogel (M-GOA) particles were synthesized, characterized, and used as a proof-of-concept in the magnetic dispersive solid phase extraction of Pb2+ ions from water samples. M-GOA was selected because is a light and porous sorbent, with high adsorption capacity, that is quickly burned by the flame. Magnetic particles were directly inserted in the flame by using a metallic magnetic probe, thereby avoiding the need for a chemical elution step. As all the extracted Pb2+ ions arrive to the flame without passing through the nebulization system, a drastic increase in the analytical signal was achieved. The improvement in the sensitivity of the proposed method (DMSS-FAAS) for Pb2+ determination was at least 40 times higher than the conventional procedure in which the Pb2+ is extracted, eluted, and analyzed by conventional flame atomic absorption spectrometry (FAAS) via the nebulization system. The analytical curve was linear from 5.0 to 180.0 μg L−1 and the limit of detection was found to be 1.30 μg L−1. Background measurements were insignificant, and the atomic absorption peaks were narrow and reproducible. Precision assessed as a percentage of the relative standard deviation %RSD was found to be 17.4, 7.1, and 7.8% for 10, 70, and 180 μg L−1 levels, respectively. The method showed satisfactory results even in the presence of other ions (Al3+, Cr3+, Co2+, Cu2+, Fe3+, Mn2+, Ba2+, Mg2+, and Li+). The performance of the new system was also evaluated for Cd2+ ions, as well as by using other magnetic particles available in our lab: magnetic carbon nanotubes (M-CNTs), magnetic restricted access carbon nanotubes (M-RACNT), magnetic poly (methacrylic acid-co-ethylene glycol dimethacrylate) (M-PMA), magnetic nanoparticles coated with orange powder peel (M-OPP), and magnetic nanoparticles covered with SiO2 (M − SiO2). Analytical signals increased for both analytes in all sorbents (increases of about 4–37 times), attesting the high potential and applicability of the proposed method. Simplicity, high analytical frequency, high detectability and reproducibility, low cost, and possibility of being totally mechanized are the most relevant advantages.

Sensitive HPLC-DMS/MS/MS method coupled with dispersive magnetic solid phase extraction followed by in situ derivatization for the simultaneous determination of multiplexing androgens and 17-hydroxyprogesterone in human serum and its application to patients with polycystic ovarian syndrome

Background and aimsAndrogens play important roles in polycystic ovarian syndrome (PCOS). However, measures of androgens based on mass spectrometry (MS) remain complex due to endogenous inferences of isomers or compounds with similar structures. Lack of sensitivity can also affect the accurate quantification of androgens, especially for very low level of 11-oxygenated androgens. Materials and methodsWe developed a fast and sensitive high-performance liquid chromatography-differential mobility spectrometry tandem mass spectrometry (HPLC-DMS/MS/MS) method for the simultaneous determination of seven androgens and 17-hydroxyprogesterone. Dispersive magnetic solid phase extraction (DMSPE) was conducted with core–shell structured nanoparticles of magnetic graphene oxide (Fe3O4@GO). In situ derivatization was performed using Girard's Reagent P. ResultsLinear ranges of the eight analytes were set in terms of clinical use. Intra- and inter-run precisions were < 16.7 % and 12.9 % for all the analytes and relative error was − 14.7–13.3 % and − 9.3–11.0 %, respectively. Extraction recoveries were 54.0–92.7 % for different analytes. The method was validated and was applied to assay 432 clinical samples. ConclusionThe developed method is green, fast, sensitive and accurate for the determination of endogenous androgens. It can be readily implemented in medical laboratories to provide superior analytical performance over the traditional electrochemiluminescence immunoassay method.

Selective capture and determination of doxycycline in marine sediments by using magnetic imprinting dispersive solid-phase extraction coupled with high performance liquid chromatography.

Antibiotics are frequently used in aquaculture as feed additives and finally enter the marine environment that can pose potential threat to humans. In this study, magnetic molecularly imprinted nanocomposites were prepared by surface imprinting and applied as selective sorbents for specific capture of doxycycline. A multivariate approach based on response surface methodology with Box-Behnken design was adopted to optimize the dispersive solid-phase extraction of doxycycline from marine sediment. Three key parameters, including adsorbent amount and type of washing/eluting solvent, were screened. Under optimum conditions, the limit of detection was 0.03μgg-1 with good linearity from 0.5 to 20μgg-1 followed by HPLC detection. Finally, two sediment samples were analysed and satisfactory recoveries between 90.60% and 93.76% were obtained with acceptable relative standard deviations (≤4.12%), suggesting a promising applicability of the developed method for efficient extraction and sensitive quantification of antibiotics in complex marine environmental matrix.

Green Synthesis of Molecularly Imprinted Polymers for Dispersive Magnetic Solid-Phase Extraction of Erythrosine B Associated with Smartphone Detection in Food Samples.

Monitoring synthetic colorants in foods is important due to their potential toxicity and pathogenicity. We propose here a new and simple method for the extraction and determination of erythrosine B (ERT-B) in food samples. A composite of polydopamine-based molecularly imprinted polymers coating magnetic nanoparticles (Fe3O4@PDA@MIP) was synthesized using a green approach and exploited for the magnetic dispersive solid-phase extraction (MDSPE) of ERT-B. Fe3O4@PDA@MIP provides a rapid extraction of ERT-B, exhibiting good reusability and preconcentration ability. Moreover, the MIP showed a relatively good imprinting factor (3.0 ± 0.05), demonstrating excellent selectivity against patent blue (an interfering dye) and other food matrix components. The proposed MDSPE was coupled to colorimetric smartphone-based detection that allowed us to obtain similar performances of UV-Vis spectroscopy detection. The smartphone-based optical detection facilitated the determination of ERT-B in the 0.5-10 mg/L range, with a limit of detection of 0.04 mg/L. The developed method was successfully employed to determine ERT-B in food samples (juice, candy, and candied cherries) with good recovery values (82-97%).

Amino acid ionic liquid–based magnetic dispersive solid-phase extraction for benzimidazole residue analysis in fruit juice and human serum based on theoretical screening

The theoretical screening and design of green solvents to reduce organic solvents and to develop green and efficient sample pretreatment methods have attracted extensive attention. Here, benzimidazoles (BZDs) with potential reproductive toxicity were used as target compounds, and amino acid ionic liquids (AAILs) were designed and selected via a theoretical calculation. With the functionalized AAIL as monomers, and POSS as the crosslinking agent, novel specific magnetic nanoparticles (Fe3O4@SiO2@MAPs@AAIL-POSS) were prepared and used to develop the magnetic dispersive solid-phase extraction (MDSPE) of trace BZDs from fruit juice and human serum. In the evaluation of the method, Fe3O4@SiO2@MAPs@AAIL-POSS showed specific adsorption, recyclable ability, high adsorption efficiency, a good recovery rate, and a low coefficient of variation. In addition, the adsorption behavior of Fe3O4@SiO2@MAPs@AAIL-POSS on BZDs was verified by investigating the kinetic and thermodynamic of the adsorption process. The study design provides ideas for green rapid detection methods of other food pollutants.

Facile and rapid preparation of magnetic octadecylamine nanocomposite and its application as a capable adsorbent in magnetic dispersive solid phase extraction of some polycyclic aromatic hydrocarbons from wastewater samples

Facile and rapid preparation of magnetic octadecylamine nanocomposite and its application as a capable adsorbent in magnetic dispersive solid phase extraction of some polycyclic aromatic hydrocarbons from wastewater samples

Theoretical design and preparation of ionic liquid-based magnetic nanoparticles for the magnetic dispersive solid-phase extraction of benzimidazoles in human plasma

Conductor-like screening model for realistic solvents (COSMO-RS) theoretical chemical model is an effective tool for predicting the thermodynamic properties of solvents. In this study, 144 ionic liquids (ILs) were designed and screened by COSMO-RS with affinity interactions with benzimidazoles (BZDs) as the target. Ionic liquid-based magnetic nanoparticles (IL-MNPs, Fe3O4@SiO2@MAPs@PIL-POSS) were prepared by the selected diene ILs (1-allyl-3-vinylimidazolium chloride [Avim]Cl) and polyhedral oligomeric silsesquioxane (POSS) coating Fe3O4 by free radical polymerization. As the adsorbent, the Fe3O4@SiO2@MAPs@PIL-POSS has great magnetic recovery ability and excellent specific adsorption ability for BZDs. The magnetic dispersive solid-phase extraction (MDSPE) of BZDs was established by optimizing the adsorption and desorption parameters. It is worth noting that the sample pretreatment only took 5 min. Combined with HPLC-MS/MS, a trace detection method for 7 trace BZDs in human plasma was established. In the method validation, the recoveries ranged from 79 % to 99 %, with relative standard deviations (RSDs) of 1.8 % to 8.8 %. The linear range were 1–1,000 μg/L. As a representative BZD, the adsorption kinetics and thermodynamic behavior of carbendazim on Fe3O4@SiO2@MAPs@PIL-POSS were analyzed to verify the adsorption mechanism, which is consistent with the results of IL screened by COSMO-RS. Therefore, it is feasible to theoretically screen IL and design IL-MNPs as specific adsorption materials. Furthermore, the theoretical design of MDSPE methods for target molecules has potential.

Preparation and application of nano petal-shaped covalent organic frameworks modified polystyrene-divinylbenzene- glycidylmethacrylate microspheres for the extraction of illicit drugs from wastewater

A novel nano petal-shaped covalent organic frameworks modified magnetic polystyrene-divinylbenzene-glycidylmethacrylate (NP-COF@Mag-PS/DVB/GMA) microsphere has been synthesized. It is a perfect combination of high productivity of PS/DVB/GMA microspheres and excellent enrichment efficiency of COF particles, and the excellent properties of NP-COF@Mag-PS/DVB/GMA microspheres are characterized by scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET) and X-ray photoelectron spectroscopy (XPS). The sorbent can extract illicit drugs via the reverse-phase interactions provided by benzene ring on the polymer backbone and the hydrogen bonding interactions provided by functional group (-NH-) on the COF particles. Based on using NP-COF@Mag-PS/DVB/GMA as sorbents, an easiness-to-handle of magnetic dispersive solid phase extraction (Mag-dSPE) procedure is proposed for the simultaneous preconcentration of 12 illicit drugs from wastewater. The obtained results show high extraction efficiency of NP-COF@Mag-PS/DVB/GMA to illicit drugs with recoveries between 81.6 and 116%. Furthermore, a liquid chromatography-tandem quadrupole mass spectrometry (LC-MS/MS) method for the determination of 12 illicit drugs from wastewater at sub-ppt levels has been proposed and validated with the pretreatment of samples by Mag-dSPE. The limits of quantification (LOQs) for the 12 illicit drugs are between 0.40 and 4.90 ng/L. Validation results on linearity, specificity, trueness and precision, as well as on application to the analysis of 12 illicit drugs in ten real samples demonstrate the applicability to environment monitoring analysis.

Graphene-Modified Magnetic Nanoparticles for Analyzing Some Pesticides Through Magnetic Dispersive Solid Phase Extraction and Dispersive Liquid–Liquid Microextraction Followed by GC–MS Determination

Graphene-Modified Magnetic Nanoparticles for Analyzing Some Pesticides Through Magnetic Dispersive Solid Phase Extraction and Dispersive Liquid–Liquid Microextraction Followed by GC–MS Determination

Correction to: Gelatin microsphere coated Fe3O4@graphene quantum dots nanoparticles as a novel magnetic sorbent for ultrasound-assisted dispersive magnetic solid-phase extraction of tricyclic antidepressants in biological samples

Correction to: Gelatin microsphere coated Fe3O4@graphene quantum dots nanoparticles as a novel magnetic sorbent for ultrasound-assisted dispersive magnetic solid-phase extraction of tricyclic antidepressants in biological samples

Rapid and sensitive analytical strategy for multi-class antibiotic residues analysis in aquatic products with amphiphilic magnetic polymer particles as an effective cleanup adsorbent

Multi-class antibiotic analysis in aquatic products is still challenging owing to the complex matrix and low co-extraction efficiency of various antibiotics. A facile and sensitive sample pretreatment method based on magnetic dispersive solid-phase extraction was thus developed via systematic optimization of extraction and purification procedure. The multi-class antibiotics can simultaneously be extracted by acetonitrile-2 % acetic acid. Amphiphilic magnetic particles and C18 were used as adsorbents to remove matrix interferences, affording significantly reduced matrix effects of analytes. Under the optimum conditions, satisfactory linearity, recovery, precision, and sensitivity were achieved. The method limits of quantification were 0.25–0.5 μg kg−1. Besides, it displayed obvious advantages in operation convenience and efficiency due to the usage of magnetic particles. The developed method was successfully used to analyze antibiotic residues in both freshwater and seafood products, manifesting its suitability for antibiotic residues analysis in aquatic products.

Vortex-assisted magnetic dispersive solid phase extraction using Tanacetum extract followed by dispersive liquid–liquid microextraction for the extraction and preconcentration of Co(II) and Ni(II) from high volume of water samples

Vortex-assisted magnetic dispersive solid phase extraction using Tanacetum extract followed by dispersive liquid–liquid microextraction for the extraction and preconcentration of Co(II) and Ni(II) from high volume of water samples

Liquid chromatographic determination of per- and polyfluoroalkyl substances in environmental river water samples

Contaminants of emerging concern (CECs) such as per- and polyfluoroalkyl substances (PFAS) have attracted significant interest from researchers, policymakers, and water treatment facilities. This is because PFAS are highly persistent in the environment and tend to be bio-accumulative thus causing adverse effects on terrestrial and aquatic life. Therefore, there is a need for simpler and fast methods for the determination of PFAS in water sources. This work aims at the application of dispersive magnetic solid-phase extraction (DMSPE) for the enrichment of PFAS in various surface water samples. Magnetic Fe3O4@MIL-101 (Cr) was used as an adsorbent in MSPE. Fe3O4@MIL-101(Cr) was used for the first time for the preconcentration and extraction of PFAS in various river water samples. The concentrations of target analytes in water samples were determined using high performance liquid chromatography-diode array detector and ultra-high performance liquid chromatography-tandem mass spectrometry analysis. The combination of optimized DMSPE with HPLC-DAD and UHPLC-MS/MS provided wide linear range (1–5000 ng/L and 0.05–2000 ng/L, low limits of detection (0.3–0.66 ng/L and 0.011–0.04 ng/L) and limits of quantification (1.0–2.2 ng/L and 0.04–0.12 ng/L). Moreover, acceptable intraday and interday precision based on the relative standard deviation (RSD) lower than 5% were obtained. The developed method showed remarkable practicability for the analysis of ultra-trace PFAS in water samples.

Magnetic silicon carbide nanocomposite as a sorbent in magnetic dispersive solid phase extraction followed by dispersive liquid–liquid microextraction in the gas chromatographic determination of pesticides

A magnetic silicon carbide nanocomposite based-magnetic dispersive solid phase extraction approach using aspiration/dispersion cycles was proposed. Several pesticides including diazinon, ametryn, chlorpyrifos, hexaconazole, diniconazole, tebuconazole, and triticonazole were extracted by this method from different samples. The analytes were extracted by a few mg of the prepared nanocomposite from the sample solution. The sample solution and adsorbent contact area was increased by performing aspiration/dispersion cycles. The nanocomposite particles were separated from sample solution using a neodymium magnet. Then an appropriate volume of an organic solvent was added onto the nanocomposite particles to desorb the analytes. Then, the obtained eluate was utilized in the next microextraction method to achieve high sensitivity and enrichment factor. Gas chromatography equipped with mass spectrometry was used for determination of the extracted analytes. Validation values considering ICH protocol illustrated that limits of detection and quantification were within the ranges of 0.06–0.33 and 0.19–1.0 ng mL−1. Good precision (relative standard deviations ≤ 7.0 %), acceptable linearity (r2 ≥ 0.992), high enrichment factors (600–850), extensive linear ranges, and acceptable extraction recoveries (60–85 %) were obtained. This approach was done on different real samples and chlorpyrifos and diazinon were determined in some of them.

Heterogeneous adsorbent based on CeZrO2 nanoparticles doped magnetic graphene oxide used for vortex assisted magnetic dispersive solid phase extraction of erythromycin in chicken

A simple, fast, and efficient method of vortex assisted magnetic dispersive solid phase extraction for separation and pre-concentration of erythromycin in chicken samples prior to high LC-UV determination has been developed. The novel heterogeneous CeZrO2 nanoparticles doped magnetic graphene oxide, for use as an efficient nanosorbent, was synthetised and applied for the adsorption of erythromycin. The synthetised nanosorbent was characterised using both Fourier-transform infra-red (FT-IR) and energy dispersive X-Ray (EDX) spectroscopy together with field emission scanning electron microscopy-EDX. To obtain the best extraction condition and maximum extraction efficiency of erythromycin, the effect of important parameters including pH, amount of sorbent, vortexing time, ionic strength, sample volume, and desorption conditions were investigated. At optimum conditions, a linear range of 0.25–300 µg kg−1, LOD (S/N = 3) of 0.079 µg kg−1, and LOQ (S/N = 10) of 0.270 µg kg−1 were obtained. The precision of the method was established as having an RSD (%) at 100 µg kg−1 of erythromycin for seven replicates of 2.6% and 3.2% for the intra-day and the inter-day, respectively. Recoveries over 94.0% confirmed a high capability of the proposed method for separation and determination of erythromycin residues in chicken being one of the most important animal products.

Ultrasound-assisted dispersive magnetic solid-phase extraction of cadmium, lead and copper ions from water and fruit juice samples using DABCO-based poly (ionic liquid) functionalized magnetic nanoparticles

A poly (ionic liquid) (PIL) functionalized magnetic nanoparticles methodology was developed and utilized as an efficient adsorbent for the simultaneous extraction of cadmium, lead, and copper ions from water and fruit juice samples. The novel adsorbent was fabricated by grafting DABCO-based PIL onto silica-coated Fe3O4 nanoparticles via copper (0)-mediated reversible-deactivation radical polymerization. Different techniques properly characterized the developed nanoparticles. The central composite design was used to analyze the simultaneous effects of various parameters on the extraction efficiency. The detection limits for water samples ranged between 3.2 and 9.2 ng.L-1, and fruit juice samples varied from 0.0103 to 0.1082 μg.kg−1. The recovery ranged from 94.1 to 101.3% and 93.6 to 105.1% for water and fruit juice samples, respectively. The relive measurement uncertainty ranged from 7.7 to 13.6%. The proposed method is rapid, sensitive, environmentally friendly, and useful for monitoring the residues of heavy metal ions in water and fruit juice samples.

Simple Synthesis of Fe3O4@-Activated Carbon from Wastepaper for Dispersive Magnetic Solid-Phase Extraction of Non-Steroidal Anti-Inflammatory Drugs and Their UHPLC–PDA Determination in Human Plasma

In the present society, the recycling and reuse of valuable substances are of utmost importance for economic and environmental purposes. At the same time, there is a pressing need to develop new methods to protect the ecosystem from many human activities, including those that have contributed to an ever-increasing presence of pharmaceutical pollutants. In this study, a straightforward approach that applies a magnetic carbon composite for the effective removal of NSAIDs from biological fluids is reported. The composite was produced by recycling wasted handkerchiefs, to provide cellulose to the reactive system and then transformed into carbon via calcination at high temperature. The morphological and structural features of the prepared “Fe3O4@-activated carbon” samples were investigated via thermal analysis, X-ray diffraction, Raman spectroscopy, and scanning electron microscopy. Magnetic solid-state extraction was carried out to reveal the adsorption capabilities of the magnetic carbon composite and then combined with UHPLC–PDA for the determination and quantification of five NSAIDs (furprofen, indoprofen, ketoprofen, flurbiprofen, and indomethacin). The method developed herein proved to be fast and accurate. The adsorbent could be reused for up to 10 cycles, without any decrease in performance; thus, it contributes to an intelligent and sustainable economic strategy projected toward minimal waste generation.