Çevik Hilal Rabia, Özyiğit Tuğçe, Kocaoğlu Arzu, Horstkotte Burkhard, Yıldırım Sercan
Karadeniz Technical University, Faculty of Pharmacy, Department of Analytical Chemistry, Farabi Street, 61080, Trabzon, Türkiye; Ondokuz Mayıs University, Faculty of Pharmacy, Department of Analytical Chemistry, Kurupelit, 55200, Samsun, Türkiye.
Karadeniz Technical University, Faculty of Pharmacy, Department of Analytical Chemistry, Farabi Street, 61080, Trabzon, Türkiye.
Talanta. 2026 Jan 1;296:128489. doi: 10.1016/j.talanta.2025.128489. Epub 2025 Jun 18.
Pharmaceutical residues in environmental waters continue to raise significant public and ecological concerns, necessitating advanced analytical methodologies for their monitoring. In this work, a novel Lab-In-Syringe automated dispersive micro solid-phase extraction (LIS-DMSPE) method was developed to determine three angiotensin receptor blockers in water samples. The approach was based on the in situ synthesis of Ni/Fe-layered double hydroxides within the void of an automatic syringe pump through controlled pH adjustment following the aspiration of precursor solutions. This enabled the rapid formation of the adsorbent and eliminated the need for pre-synthesized or magnetized sorbents. Enhanced sedimentation speed, achieved by increasing ionic strength with NaNO, allowed isolating the sedimented sorbent from the sample matrix without centrifugation and filtration. The instrumental setup was successfully coupled online with HPLC-DAD. After in-syringe washing and dissolving the sediment, the low organic solvent content of the extract enabled large-volume injection (200 μL), thereby boosting sensitivity. Parameters including type and volume of precursor solution, NaNO addition, buffer volume and pH, stirring rate and time, and the composition of elution/destruction solution were carefully optimized. Recoveries and enrichment factors were in the ranges of 62.0-88.7 % and 13.3-25.8, respectively. The method was linear over a 5-200 μg L concentration range for all analytes. Accuracies ranged from 88.7 % to 105.8 % for real samples spiked at two concentrations with RSDs less than 3.5 %. To our knowledge, this is the first report on a LIS-DMSPE method that does not require pre-synthesis or magnetization of the sorbent for extraction and uses accelerated sedimentation for adsorbent isolation.
环境水体中的药物残留持续引发重大的公众和生态担忧,因此需要先进的分析方法对其进行监测。在本研究中,开发了一种新型的注射器内实验室自动分散微固相萃取(LIS-DMSPE)方法,用于测定水样中的三种血管紧张素受体阻滞剂。该方法基于在自动注射泵的空隙内通过吸入前体溶液后控制pH值原位合成镍/铁层状双氢氧化物。这使得吸附剂能够快速形成,并且无需预先合成或磁化吸附剂。通过添加硝酸钠增加离子强度提高了沉降速度,从而无需离心和过滤即可从样品基质中分离沉淀的吸附剂。该仪器装置成功地与高效液相色谱-二极管阵列检测器(HPLC-DAD)在线联用。在注射器内洗涤并溶解沉淀后,提取物的低有机溶剂含量允许进行大体积进样(200 μL),从而提高了灵敏度。对前体溶液的类型和体积、硝酸钠添加量、缓冲液体积和pH值、搅拌速率和时间以及洗脱/破坏溶液的组成等参数进行了仔细优化。回收率和富集因子分别在62.0-88.7%和13.3-25.8范围内。该方法对所有分析物在5-200 μg/L的浓度范围内呈线性。在两个浓度水平加标的实际样品中,准确度范围为88.7%至105.8%,相对标准偏差小于3.5%。据我们所知,这是第一篇关于LIS-DMSPE方法的报道,该方法在萃取时无需对吸附剂进行预合成或磁化,并且使用加速沉降来分离吸附剂。