Department of Chemistry, Semnan University, Semnan 35195-363, Iran.
Department of Chemistry, Semnan University, Semnan 35195-363, Iran.
J Chromatogr B Analyt Technol Biomed Life Sci. 2019 Jan 1;1104:196-204. doi: 10.1016/j.jchromb.2018.11.008. Epub 2018 Nov 7.
For the first time, three phase hollow fiber liquid phase microextraction using an influential, and green middle phase comprised a new relatively-hydrophobic deep eutectic solvent (three-phase HF-LPME-DES) was developed for trace analyses of antiarrhythmic drugs in biological and environmental samples. The extraction solvent was easily synthesized by mixing the green and cheap raw materials, namely choline chloride and 1-phenylethanol (ChCl: Ph-ETOH), in the ambient temperature. Good compatibility to pores of hollow-fiber, high ability for extraction of ionizable organic compounds with no need to any carrier agents, and easy availability in the laboratory environment turned this new proposed deep eutectic intermediate to a worthy generation of the supported liquid membrane (SLM). Final determination was accurately done by high performance liquid chromatography-ultraviolet detection (HPLC-UV). After effective statistical optimization of main parameters, the valid analytical features were found to be: wide linear dynamic ranges (LDRs) of 0.8 to 500 ng mL with the determination coefficients (Rs) higher than 0.98, low detection limits (LODs) of 0.3-0.8 ng mL, and logical precision (relative standard deviations (%RSDs, n = 3) of 5.2-6.5%). Also, enrichment factors and extraction recoveries were 110-135 and 44-54%, respectively. These satisfactory results confirmed the potent effectiveness of the proposed microextraction procedure for achievement to clean and proper enrichment of the aforesaid compounds in highly complex real samples.
首次开发了一种使用有影响力且环保的中间相的三相中空纤维液相微萃取法,该中间相由一种新型相对疏水性的深共晶溶剂(三相 HF-LPME-DES)组成,用于痕量分析生物和环境样品中的抗心律失常药物。萃取溶剂是通过在环境温度下混合绿色且廉价的原料,即氯化胆碱和 1-苯乙醇(ChCl:Ph-ETOH)来轻松合成的。这种新提出的深共晶中间相与支持液膜(SLM)具有良好的中空纤维孔相容性、对可离子化有机化合物的高萃取能力、无需任何载体试剂,并且在实验室环境中易于获得。最终通过高效液相色谱-紫外检测(HPLC-UV)进行准确测定。在对主要参数进行有效统计优化后,发现有效的分析特征为:线性动态范围(LDRs)为 0.8 至 500ng/mL,相关系数(Rs)高于 0.98,检测限(LODs)为 0.3-0.8ng/mL,以及合理的精密度(相对标准偏差(%RSDs,n=3)为 5.2-6.5%)。此外,富集因子和萃取回收率分别为 110-135 和 44-54%。这些令人满意的结果证实了所提出的微萃取程序在实现上述化合物在高度复杂的实际样品中的清洁和适当富集方面的强大有效性。