Electromembrane extraction using biodegradable deep eutectic solvents and agarose gel as green and organic solvent-free strategies for the determination of polar and non-polar bases drugs from biological samples: A comparative study

Autor: Hamdollah Abbasi, Shahryar Abbasi, Seyed Ammar Haeri, Sobhan Rezayati, Fatemeh kalantari, Mohammad Reza Poor Heravi
Rok vydání: 2022
Předmět:
Zdroj: Analytica Chimica Acta. 1222:339986
ISSN: 0003-2670
DOI: 10.1016/j.aca.2022.339986
Popis: Two modes of electromembrane extraction (EME) were evaluated in this work, one using deep eutectic solvents (DESs) as liquid membrane, and another was gel electromembrane extraction (G-EME) based on solid agarose membrane. Both EME modes have eliminated organic solvents and are recognized as green strategies. Unlike classic EME in which polypropylene membrane and organic extracting solvents play an essential role in the extraction process, new modes of EME are based on biodegradable membranes and aqueous extracting solutions. Approaches of EME based on the new designs follow the green chemistry principles. Each mode of EME was evaluated for the determination of polar and non-polar bases drugs from human urine samples using high-performance liquid chromatography (HPLC) equipped with a diode array detector (DAD). EME using DES A was suitable for determining polar and non-polar bases drugs in a large polarity window. While extraction recoveries for all six drugs studied by G-EME were lower than EME using DES A. Comparing the two EME modes shows similar results in the analytical figures of merit. However, differences in extraction recoveries of the drugs by two EME modes were observed which is related to the difference in membranes structure. Our findings indicate that the differences between membranes properties used in two EME modes, including the permeability, hydrophilicity, hydrophobicity, and variety of interactions, are influencer factors on extraction efficiency. The two EME modes provided good linearity in the ranges of 16-100 and 19-100 μg. L
Databáze: OpenAIRE