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Magnetic cellulose nanoparticles (MCNPs) were used for the first time as sorbents for stir bar-sorptive dispersive microextraction (SBSDME). The main experimental parameters involved in the SBSDME process that affect extraction (i.e. amount of MCNPs, ionic strength, pH, extraction and back-extraction time) were investigated. The method was applied to the determination of nine polychlorinated biphenyls (PCBs) in fruit juice samples by gas chromatography-mass spectrometry (GC-MS). Under the optimized conditions, a good linearity was obtained in a concentration range of 10-1000 ng mL -1 with determination coefficients over 0.9945. Limits of detection and quantification for all target PCBs were in the range 2.1-54 ng L -1 and 7.0-180 ng L -1 , respectively. Intra-day precision ranged from 1.7% to 8.8% and inter-day precision from 3.4% to 9.3% RSD. The enrichment factors of the analytes were from 74.6 to 98.2. The MCNPs can be reused up to 5 times. The method was applied to commercial orange and pineapple juices (n = 5), where concentrations were below the limits of detection. Recoveries from 70.4 to 108.0% were obtained by applying the method for the analysis of spiked fruit juice samples at 1 and 2 ng mL -1 concentration levels. The use of cellulose makes this approach environmentally friendly and the magnetism of the resulting sorbent in conjunction with SBSDME provides ease of handling and saving of time., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Magnetic cellulose nanoparticles (MCNPs) coated with 1-butyl-3-methylimidazolium hexafluoro phosphate [C 4 MIM][PF 6 ] ionic liquid (IL) through electrostatic interactions are proposed for the first time as sorbents in a magnetic solid phase extraction (MSPE) method for the determination of paracetamol (PAR), ibuprofen (IBU), naproxen (NAP) and diclofenac (DIC) in natural waters. The parameters that affect adsorption (dispersive solvent, amount of IL, pH and salt content) and desorption (desorption solvent, type of energy and time) were studied. The values that provided the maximum adsorption efficiency and extraction recovery were selected as optimum conditions for adsorption and desorption, respectively. Under the optimum conditions, the adsorption and desorption of all analytes was simultaneous and quantitative. High performance liquid chromatography (HPLC) with ultra violet (UV) and fluorescence (FL) detector was used after the sample preparation. The precision, expressed as relative standard deviation was between 1.4 and 7.6%. Limits of detection and quantification were in the range 3.2–7.2 μg L − 1 and 11–24 μg L − 1 , respectively. Moreover, the proposed method provides enrichment factors from 29.0 to 34.2. Recovery studies on 10 mL of spiked tap, river and dam water samples at 50 and 100 μg L − 1 were carried out. The extraction recoveries were from 85 to 116%, and were in a comparable range regardless of the type of water. The method is simple, rapid, and environmentally friendly. [ABSTRACT FROM AUTHOR]