利用聚多巴胺包被微纤维吸附剂的可编程流心脏切割固相萃取作为UHPLC的前端,用于直接测定地表水中的异种生物残留物

IF 5.6 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Lucie Chocholoušová Havlíková , Petr Chocholouš , Jakub Erben , Pavel Holec , František Švec , Dalibor Šatínský
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引用次数: 0

摘要

采用自动化和多步骤联线法对地表水中外生菌残留进行了灵敏测定。在线连线序进样分析仪器采用表面改性微纤维吸附剂对1.0 mL样品进行有效固相萃取,萃取至100 μL区域,然后进行反相超高高效液相色谱(SIA-SPE-UHPLC)。用聚丙烯微纤维填充固相萃取柱,用多巴胺溶液冲洗后包被聚多巴胺。采用SIA-SPE-UHPLC法对200多个样品进行了高重复性的提取。基质标度在预期范围内,检出限在0.1 ~ 0.9 μg/L。方法精密度为13% RSD(3个浓度水平),准确度在86.5 ~ 114.8%范围内。当分离时间为12 min时,该方法的样品吞吐量为5个样品/小时,其中包括平行运行下一个样品的5 min SPE步骤。通过对15个河流水样进行分析,证明了该方法的性能,这些水样中添加了11种典型监测水平的外源药物(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)。自动分析前的初始样品处理仅包括甲醇添加、pH调整和离心。在歧管和过程的创新,有助于现代和有效的分析环境样品进行了讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Programmable flow heart cutting solid phase extraction using polydopamine coated microfibrous sorbent as a front-end to UHPLC for direct determination of xenobiotic residues in surface water

Programmable flow heart cutting solid phase extraction using polydopamine coated microfibrous sorbent as a front-end to UHPLC for direct determination of xenobiotic residues in surface water
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.
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来源期刊
Talanta
Talanta 化学-分析化学
CiteScore
12.30
自引率
4.90%
发文量
861
审稿时长
29 days
期刊介绍: Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome. Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.
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