Chocholoušová Havlíková Lucie, Chocholouš Petr, Erben Jakub, Holec Pavel, Švec František, Šatínský Dalibor
Charles University, Faculty of Pharmacy in Hradec Králové, Department of Analytical Chemistry, Akademika Heyrovského 1203, 50003, Hradec Králové, Czechia.
Charles University, Faculty of Pharmacy in Hradec Králové, Department of Analytical Chemistry, Akademika Heyrovského 1203, 50003, Hradec Králové, Czechia.
Talanta. 2025 Jul 11;297(Pt A):128571. doi: 10.1016/j.talanta.2025.128571.
Automation and hyphenation of multiple steps were used for the sensitive determination of xenobiotic residues in surface waters. The online hyphenated sequential injection analysis instrumentation used surface-modified microfibrous sorbent for the effective solid phase extraction of 1.0 mL of sample into 100 μL zone, then subjected to the reversed-phase ultra-high performance liquid chromatography (SIA-SPE-UHPLC). The SPE column was packed with polypropylene microfibers and coated with polydopamine by rinsing with the dopamine solution. The freshly prepared column was used for highly reproducible extraction of more than 200 samples in the SIA-SPE-UHPLC method. The matrix calibration covered the expected range with limits of detection in the range 0.1-0.9 μg/L. The method precision was <13 % RSD (at 3 concentration levels), and the method accuracy was in the range 86.5-114.8 %. The sample throughput of the method was 5 samples/hour when the separation took 12 min, including a 5 min SPE step of the next sample run in parallel. The performance of the developed method was demonstrated with the analysis of fifteen river water samples spiked with eleven residues of xenobiotics (ivermectin, fenbendazole, praziquantel, ibuprofen, diclofenac, 17α-ethynylestradiol, androstenedione, carbamazepine, omeprazole, sotalol, and caffeine) at the levels typical for such monitoring. Initial sample treatment prior to the automated analysis consisted only of methanol addition, pH adjustment, and centrifugation. The innovations in the manifold and process that contribute to the modern and effective analysis of environmental samples are discussed.
采用多步骤自动化和连字符连接技术对地表水中的外源性残留进行灵敏测定。在线连字符连接顺序注射分析仪器使用表面改性的微纤维吸附剂,将1.0 mL样品有效固相萃取至100 μL区域,然后进行反相超高效液相色谱分析(SIA-SPE-UHPLC)。固相萃取柱填充有聚丙烯微纤维,并用多巴胺溶液冲洗以涂覆聚多巴胺。新制备的柱子用于SIA-SPE-UHPLC方法中200多个样品的高度可重复萃取。基质校准覆盖预期范围,检测限在0.1-0.9 μg/L范围内。方法精密度<13%相对标准偏差(在3个浓度水平下),方法准确度在86.5-114.8%范围内。当分离时间为12分钟时,该方法的样品通量为5个样品/小时,包括并行运行下一个样品的5分钟固相萃取步骤。通过分析15个添加了11种外源性残留(伊维菌素、芬苯达唑、吡喹酮、布洛芬、双氯芬酸、17α-乙炔雌二醇、雄烯二酮、卡马西平、奥美拉唑、索他洛尔和咖啡因)的河水样品,验证了所开发方法在这种监测典型水平下的性能。自动化分析前的初始样品处理仅包括添加甲醇、调节pH值和离心。讨论了有助于对环境样品进行现代有效分析的流路和过程中的创新。