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A novel and simple air-assisted liquid-liquid microextraction (AALLME) is introduced to analyze the organophosphorus pesticide (OPP) residues in fruit juice samples, using the gas chromatography-flame photometric detection (GC-FPD). In this method, fine extraction solvent drops are rapidly formed and dispersed into the aqueous samples, by using a syringe to withdraw and push-out the mixture of aqueous sample solution and extraction solvent several times. The parameters affecting the extraction efficiency were investigated including the type and volume of the extraction solvent, salt addition, extraction times, and pH. Under optimized conditions, the method showed good linearities with the correlation coefficients (γ) higher than 0.9988, and the sensitivity with the limits of detection (LODs) between 0.02μgL(-1) and 0.6μgL(-1). The method was applied to determine the OPP residues in juice samples and the recoveries were ranged from 79% to 113% with relative standard deviations (RSDs) of 0.4-9.9%. The feasibility of the method in real samples was proved., (Copyright © 2013 Elsevier B.V. All rights reserved.)

A simple and efficient directly suspended droplet microextraction (DSDME) has been developed to extract and pre-concentrate organochlorine and pyrethrin pesticides from tea samples prior to analysis by a gas chromatography-electron capture detector (GC-ECD). The optimal experimental conditions of DSDME were: 100 μL isooctane exposed for 15 min to 5 mL of the tea aqueous sample stirred at 1100 rpm. For most of the target analytes, the optimal pretreatment of DSDME processes led to no significant interference of tea matrices. The approach was applied to the determination of organochlorine and pyrethroid pesticides in tea samples, with a linearity range of 0.0005-2 μg/mL. The relative recoveries of all the pesticides ranged between 80.0% and 120.8% with relative standard deviations (RSDs) in the range of 0.8-19.9% (n=5). The limits of detections (LODs) ranged between 0.04 and 1 μg/L for all the target pesticides., (Copyright © 2012 Elsevier B.V. All rights reserved.)