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建立了首个完全优化和验证的 SPE-LC-MS/MS 方法,用于测定地表水中新一代新烟碱类农药。

The first fully optimized and validated SPE-LC-MS/MS method for determination of the new-generation neonicotinoids in surface water samples.

机构信息

Department of Environmental Analysis, Faculty of Chemistry, University of Gdańsk, Ul. Wita Stwosza 63, 80-308, Gdańsk, Poland.

Department of Environmental Analysis, Faculty of Chemistry, University of Gdańsk, Ul. Wita Stwosza 63, 80-308, Gdańsk, Poland.

出版信息

Chemosphere. 2023 Jan;310:136868. doi: 10.1016/j.chemosphere.2022.136868. Epub 2022 Oct 17.

Abstract

Widespread use of the new generation neonicotinoids (NQs) results in their constant inflow to water bodies. Both their persistence in waters and mechanism of action similar to older compounds already banned in the EU raise concerns about potential ecotoxicological effects. Information about presence of the new NQs in the aquatic environment is still sparse, and the consequences for aquatic organisms remain mostly unknown, due to the lack of sensitive and selective analytical tools. Therefore, a method utilizing solid-phase extraction and liquid chromatography-tandem mass spectrometry (SPE-LC-MS/MS) has been developed and optimized, enabling the monitoring of EU-approved NQs: acetamiprid (ACT), sulfoxaflor (SFX) and flupyradifurone (FLU), and common NQ metabolite 6-chloronicotinoic acid (6-CNA) in surface waters. To optimize their extraction from natural water samples, the response surface methodology (RSM) was used. An increase in pH value favored higher absolute recoveries (AR) of ACT, SFX and FLU, while the opposite effect was observed for 6-CNA. Increasing water sample volume had adverse effect on the extraction of all compounds. The optimal conditions for simultaneous extraction of all compounds included the use of Oasis HLB sorbent, 200 mL of a water sample at pH of 4.6, and application of 0.3% HCOOH in acetonitrile as an eluent, allowing to obtain AR values above 80% in most cases. Further increase in pH value had positive impact on extraction effectiveness of ACT, SFX and FLU. The method was subjected to full matrix-matched validation and was proven to be fully reliable for the analysis of ACT, SFX and FLU, while the successful isolation of 6-CNA depends on the matrix composition. Finally, the method was applied to the analysis of NQs in surface water samples, proving its sensitivity and selectivity. It can be easily adapted as a tool for trace analysis of NQs and for NQ-associated risk assessment in aquatic ecosystems.

摘要

新一代新烟碱类(NQs)的广泛使用导致其不断流入水体。它们在水中的持久性及其作用机制与欧盟已禁用的旧化合物相似,这引起了人们对潜在生态毒理学影响的关注。关于新 NQs 在水生环境中的存在的信息仍然很少,由于缺乏敏感和选择性的分析工具,水生生物的后果在很大程度上仍然未知。因此,已经开发并优化了一种利用固相萃取和液相色谱-串联质谱(SPE-LC-MS/MS)的方法,能够监测欧盟批准的 NQs:乙虫腈(ACT)、噻虫氟(SFX)和氟啶虫酰胺(FLU),以及常见的 NQ 代谢物 6-氯烟碱酸(6-CNA)在地表水。为了优化它们从天然水样中的提取,使用了响应面法(RSM)。pH 值的增加有利于 ACT、SFX 和 FLU 的绝对回收率(AR)更高,而 6-CNA 的情况则相反。增加水样体积对所有化合物的提取都有不利影响。同时提取所有化合物的最佳条件包括使用 Oasis HLB 吸附剂、pH 值为 4.6 的 200 mL 水样,以及应用 0.3%甲酸在乙腈中的洗脱剂,在大多数情况下可获得高于 80%的 AR 值。进一步增加 pH 值对 ACT、SFX 和 FLU 的提取效果有积极影响。该方法经过全矩阵匹配验证,被证明完全可靠,可用于 ACT、SFX 和 FLU 的分析,而 6-CNA 的成功分离取决于基质组成。最后,该方法应用于地表水样品中 NQs 的分析,证明了其灵敏度和选择性。它可以很容易地适应作为痕量分析 NQs 和评估水生生态系统中 NQ 相关风险的工具。

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