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This manuscript presents a new method for selective extraction and determination of fosetyl-aluminum in fruits and vegetable samples based on ultrasonic-assisted dispersive liquid-liquid microextraction method using ionic liquids (IL-UA-DLLME). A UV-Visible spectrophotometer was used for detection and quantification. Plants used for sample collection were grown under controlled conditions in a greenhouse. Central composite design (CCD)-response surface methodology (RSM) analysis was used for the optimization of significant factors (volume of IL, pH, ultrasonication time, and THF volume). Under optimal conditions, the limit of detection and limit of quantification of the IL-UA-DLLME procedure were 1.5 ng mL−1 and 5.0 ng mL−1 respectively with relative standard deviation 1.9–3.3%. The developed IL-UA-DLLME procedure demonstrated linearity within the concentration range of 5–600 ng mL−1 with an R2 value of 0.9914. The enrichment factor was 114 with a recovery% of 94.2–98.6% (n = 3) at optimal conditions. The IL-UA-DLLME assay was used for the analysis of fosetyl-aluminum in a variety of food samples and was found highly selective and efficient. [Display omitted] • Ionic liquid-based pre-concentration method for fosetyl-aluminum analysis in foods. • Increased mass transfer via DLLME for fungicide isolation from plant material. • Fully validated method with proved applicability to real samples and routine analysis. • A highly sensitive, selective, and robust assay for environmental monitoring. • Fast analyte isolation followed by spectroscopic final determination stage [ABSTRACT FROM AUTHOR]

In this paper, a green, cost-effective sample preparation method based on air assisted liquid phase microextraction (AA-LPME) was developed for the simultaneous extraction of As(III) and Sb(III) ions from vegetable samples using hydrophilic/hydrophobic natural deep eutectic solvents (NADESs). Central composite design was used for the optimization of extraction factors including NADES volume, extraction cycle, pH, and curcumin concentration. Limits of detection for As(III) and Sb(III) were 1.5 ng L−1 and 0.06 ng L−1, respectively. Working ranges for As(III) and Sb(III) were 0.2–300 ng L−1 (coefficient of determination (R2 = 0.9978) and 5–400 ng L−1 (R2 = 0.9996), respectively. Relative standard deviations for As(III) and Sb(III) were 2.2–2.8% and 2.9–3.2%, respectively. Enrichment factor of the method was 184 for As(III) and 172 for Sb(III). The accuracy and precision of the AA-NADES-LPME method were investigated by intraday/interday studies and standard reference material analysis, respectively. Finally, the AA-NADES-LPME method was successfully applied to microwave digested vegetable samples using the standard addition approach and acceptable recoveries were achieved. [Display omitted] • α-terpineol and octanoic acid-based NADES was prepared as extraction solvent. • The microextraction step was faster and did not require centrifugation and heating step. • The interaction between analytes and ligand was explained by computational study. • The method showed high sensitivity for As(III) and Sb(III). [ABSTRACT FROM AUTHOR]