Department of Analytical Chemistry, Institute of Chemistry, Saint-Petersburg University, St. Petersburg State University, SPbSU, SPbU, 7/9 Universitetskaya nab., St. Petersburg, 199034 Russia.
Department of Analytical Chemistry, Institute of Chemistry, Saint-Petersburg University, St. Petersburg State University, SPbSU, SPbU, 7/9 Universitetskaya nab., St. Petersburg, 199034 Russia.
Talanta. 2022 Dec 1;250:123709. doi: 10.1016/j.talanta.2022.123709. Epub 2022 Jun 23.
An effervescence-assisted dispersive liquid-liquid microextraction approach using three-component deep eutectic solvent based on short-chain and medium-chain carboxylic acids and terpenoid was developed for the first time. The microextraction procedure was applied to the determination of fluoroquinolone antibiotics in foods (milk and shrimp samples) by high-performance liquid chromatography with fluorometric detection. In this microextraction procedure three-component deep eutectic solvent acted as a proton donor agent and an extractant. The carbon dioxide bubbles caused by the fast reaction between precursor of deep eutectic solvent (short-chain carboxylic acid) and effervescent agent (sodium carbonate) promoted the dispersion of the extractant in an aqueous sample phase. Various carboxylic acids were studied as hydrogen bond donors for the formation of deep eutectic solvents and proton donor agents for the generation of CO bubbles. Two natural terpenoids (menthol and thymol) were studied as the hydrogen bond acceptors for the formation of three-component solvent. The extraction system based on heptanoic acid and thymol (1:2, mol/mol) containing formic acid (proton donor for generating CO bubbles) provided maximum extraction recovery (86-99%) and a higher extraction efficiency of analytes compared to their extraction into individual hydrophobic precursors of the system. The LODs, calculated from the blank tests based on 3σ, were varied from 0.03 to 0.06 μg L and from 0.3 to 0.6 μg kg for fluoroquinolone antibiotics in milk and shrimp samples, respectively. The proposed approach provided effective dispersion of extractant speeding up the extraction process and fast separation of phases without any external energy assistance.
首次开发了一种基于短链和中链羧酸和萜烯的三元深共晶溶剂的自发辅助分散液 - 液微萃取方法。该微萃取程序用于通过高效液相色谱法与荧光检测法测定食品(牛奶和虾样品)中的氟喹诺酮类抗生素。在该微萃取程序中,三元深共晶溶剂作为质子供体试剂和萃取剂。深共晶溶剂(短链羧酸)的前体与发泡剂(碳酸钠)之间的快速反应产生的二氧化碳气泡促进了萃取剂在水相样品中的分散。研究了各种羧酸作为氢键供体以形成深共晶溶剂和质子供体试剂以产生 CO 气泡。两种天然萜烯(薄荷醇和百里酚)被研究为形成三元溶剂的氢键受体。基于庚酸和百里酚(1:2,摩尔/摩尔)的萃取体系,其中含有甲酸(生成 CO 气泡的质子供体),与该体系的单个疏水性前体相比,提供了最大的萃取回收率(86-99%)和更高的分析物萃取效率。LODs 基于 3σ 从空白试验计算,分别为牛奶和虾样品中氟喹诺酮类抗生素的 0.03-0.06μg L 和 0.3-0.6μg kg。该方法提供了有效的萃取剂分散,加速了萃取过程,并在没有任何外部能量辅助的情况下快速分离相。