Ionic liquid-based aqueous two-phase extraction as a pretreatment strategy for the determination of 38 pharmaceuticals and personal care products in aquatic environments by HPLC-MS/MS

IF 4 2区 化学 Q1 BIOCHEMICAL RESEARCH METHODS
Journal of Chromatography A Pub Date : 2026-02-22 Epub Date: 2026-01-02 DOI:10.1016/j.chroma.2026.466670
Shuo Xie , Wenbin Zhang , Yike Han , Xinyan Dong , Wanning Li , Penghui Li , Liyun Kong
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Abstract

The accurate determination of pharmaceuticals and personal care products (PPCPs) in wastewater is crucial for comprehensive environmental risk assessment and human exposure evaluation. Given the complex matrices of aqueous environmental samples, efficient sample preparation remains a critical challenge in analytical procedures. This study presents an ionic liquid-based aqueous two-phase system (IL-ATPS) extraction methodology used as a pretreatment step prior to high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) for the simultaneous determination of 38 PPCPs. A mechanistic investigation revealed that target analytes with more hydrogen-bonding sites and higher hydrogen-bond donor (HBD) capacity exhibited enhanced solubility in ILs. In addition, IL anions with stronger hydrogen-bond acceptor (HBA) capacity further improved the solubility of the 38 PPCPs. These findings indicate that hydrogen bonding between analytes and ILs likely played a critical role in the dissolution mechanism. The established IL-salt ATPS extraction method utilized a 15 mL aqueous sample, 0.2 g tetraethylammonium acetate ([N2222][OAc]), and 12 g K2HPO4, with a 1-minute vortex mixing. Compared with traditional solid phase extraction (SPE), this approach significantly reduced the sample volume from 1 L to 15 mL, avoided the use of volatile organic solvents, simplified the overall processing, and enabled rapid (<15 minutes) pretreatment. The method demonstrated excellent sensitivity with limits of detection (LODs) ranging from 0.00013 to 0.11 ng/mL. Method validation via standard addition experiments demonstrated satisfactory accuracy, yielding recoveries between 74.3 and 129.8 %. Precision was assessed using both intra-day and inter-day measurements. The intra-day relative standard deviations (RSDs) ranged from 0.7 % to 19.9 %, while the inter-day RSDs ranged from 1.4 % to 18.4 %, demonstrating that the method provides consistent and reproducible results under controlled laboratory conditions. These findings underscore the present IL-based ATPS extraction method, followed by HPLC-MS/MS analysis, as an eco-friendly, robust, and scalable approach for PPCPs monitoring in aqueous environmental samples, offering potential applications in environmental monitoring and risk assessment.
离子液体基双水相萃取预处理技术用于测定水生环境中38种药品和个人护理用品的HPLC-MS/MS。
准确测定废水中药品和个人护理产品(PPCPs)的含量对综合环境风险评估和人体暴露评价至关重要。鉴于水环境样品的复杂基质,有效的样品制备仍然是分析过程中的关键挑战。本研究提出了一种离子液体基水两相体系(IL-ATPS)提取方法,作为高效液相色谱-串联质谱(HPLC-MS/MS)同时测定38种PPCPs的预处理步骤。一项机制研究表明,具有更多氢键位点和更高氢键供体(HBD)容量的目标分析物在il中的溶解度增强。此外,具有较强氢键受体(HBA)容量的IL阴离子进一步提高了38 PPCPs的溶解度。这些发现表明,分析物与il之间的氢键可能在溶解机制中起关键作用。建立的il -盐ATPS提取方法使用15 mL水样,0.2 g乙酸四乙铵([N2222][OAc])和12 g K2HPO4,涡旋混合1分钟。与传统固相萃取(SPE)相比,该方法将样品体积从1 L显著减少到15 mL,避免了挥发性有机溶剂的使用,简化了整个过程,实现了快速(
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来源期刊
Journal of Chromatography A
Journal of Chromatography A 化学-分析化学
CiteScore
7.90
自引率
14.60%
发文量
742
审稿时长
45 days
期刊介绍: The Journal of Chromatography A provides a forum for the publication of original research and critical reviews on all aspects of fundamental and applied separation science. The scope of the journal includes chromatography and related techniques, electromigration techniques (e.g. electrophoresis, electrochromatography), hyphenated and other multi-dimensional techniques, sample preparation, and detection methods such as mass spectrometry. Contributions consist mainly of research papers dealing with the theory of separation methods, instrumental developments and analytical and preparative applications of general interest.
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