Green approaches with amino acids-based deep eutectic solvents (AADES) for determining As in medicinal herbs by ICP-MS

• Published in: Journal of molecular liquids 2023-07, Vol.381, p.121801, Article 121801
• Main Authors: Guimarães, Taciana G.S., Costa, Floriatan Santos, Menezes, Iohanna M.N.R., Santana, Ana P.R., Andrade, Daniel F., Oliveira, Andrea, Amaral, Clarice D.B., Gonzalez, Mario H.
• Format: Article
• Language: English
• Subjects: Deep eutectic solvent; Green analytical chemistry; Microwave-assisted extraction (MAE); Multivariate optimization; Ultrasound-assisted matrix solid-phase dispersion (UA-MSPD)
• ISSN: 0167-7322; 1873-3166
• DOI: 10.1016/j.molliq.2023.121801

[Display omitted] •Green solvents were applied in sample preparation methods.•A new ultrasound-assisted matrix solid-phase dispersion method based on AADES was developed (UA-MSPD/AADES).•UA-MSPD does not require prior synthesis of AADES.•The optimum experimental conditions for UA-MSPD and MAE were obtained using Doehlert designs.•The consumption of medicinal samples is safe in terms of As content. In this work, an innovative ultrasound-assisted matrix solid-phase dispersion (UA-MSPD) method and microwave-assisted extraction (MAE) were applied with amino acids-based deep eutectic solvents (AADES) for the extraction of arsenic (As) from medicinal herbs. Multivariate optimization by Doehlert design (DD) was performed to determine the optimal experimental conditions. The effects of temperature (TP), time (TM), and sample-solvent ratio (SSR) were evaluated, and the optimized conditions were 50 °C, 60 min, and 10:1 mg mL−1 for UA-MSPD and 100 °C, 40 min, and 40:1 mg mL−1 for MAE, employing AADES 2 (β-alanine, citric acid, and water), where the hydroxyl and carboxyl groups of the citric acid structure favored formation of a chelate complex with the analyte. AADES 3 (β-alanine, xylitol, and water) was effective for MAE, while AADES 1 (β-alanine, malic acid, and water) proved to be inefficient for As extraction. The parameters of the analytical methods were evaluated using certified reference materials. The accuracy, based on percentage recovery, was in the range 77–101 %, while the limits of detection and quantification were in the ranges 0.010–0.039 mg kg−1 and 0.011–0.130 mg kg−1, respectively. The analytical curves presented R2 > 0.99. The proposed methods were shown to be environmentally friendly, based on the Analytical Eco-Scale and RGB 12 procedures. Both optimized methods were applied for the determination of As in commercial medicinal herbs (0.059–0.101 mg kg−1), with the values obtained being within the maximum daily intake limit established by the World Health Organization (WHO). It should be noted that there are no previous reports in the literature concerning the application of a sample preparation method using AADES, employing their solid precursors, with no requirement for prior solvent synthesis, as proposed here in the case of the UA-MSPD method.