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直接浸入式 SPME-LC-Tips 提取土壤中的农药,然后进行 GC-MS/MS 分析:评估与概念验证。

Extraction of pesticides from soil using direct-immersion SPME LC-Tips followed by GC-MS/MS: Evaluation and proof-of-concept.

机构信息

CENSE - Center for Environmental and Sustainability Research & CHANGE - Global Change and Sustainability Institute, NOVA School of Science and Technology, NOVA University Lisbon, 2829-516 Caparica, Portugal.

CENSE - Center for Environmental and Sustainability Research & CHANGE - Global Change and Sustainability Institute, NOVA School of Science and Technology, NOVA University Lisbon, 2829-516 Caparica, Portugal.

出版信息

J Chromatogr A. 2024 Oct 25;1735:465295. doi: 10.1016/j.chroma.2024.465295. Epub 2024 Aug 29.

Abstract

A new method was evaluated and developed for the analysis of pesticides in sandy-loam soil by direct-immersion solid phase microextraction (DI-SPME) followed by gas chromatography tandem-mass spectrometry (GC-MS/MS) determination. Ten pesticides were selected based on a literature survey of the compounds reported to be present in EU soils. The extraction was performed using SPME LC-Tips, a new SPME configuration with the coated fibers attached to a disposable and easy-to-handle micropipette tip, which was immersed into a soil slurry made by the addition of an aqueous solution to the soil sample. Ten experimental parameters were evaluated with a Plackett-Burman design, after which the extraction time and percentage of organic solvent in the aqueous extraction were optimized separately. The two fiber chemistries available (PDMS/DVB and C) were evaluated in parallel for the entire work. In the final method, slurry samples were made by adding an aqueous solution (6 % methanol v/v) to 2 g of soil. The fiber was conditioned and then inserted, for extraction, into the samples, stirred by a magnetic bar. Afterwards, the analytes were desorbed onto 100 µL of methanol. After the addition of analyte protectants (ethylglycerol, gulonolactone, and sorbitol) the extract was injected into the GC-MS/MS system. Isotopically labelled penconazole was used as internal standard. A calibration was performed by extracting spiked soil with analyte concentrations of 0.1-50 µg/kg. Coefficients of determination of the linear calibration were between 0.94-0.98 for the PDMS/DVB and 0.92-0.99 for the C. Limits of detection range between 0.01-10 µg/kg for the PDMS/DVB and 0.1-10 µg/kg for the C. Overall, the C analytically outperformed the PDMS/DVB but required a longer extraction time (120 min vs 75 min for the PDMS/DVB). This method allows automation and generates low residual toxic waste, having the potential to be introduced as a greener and simpler alternative to currently used sample preparation methodologies.

摘要

一种新的方法被评估和开发,用于通过直接浸入式固相微萃取(DI-SPME)分析沙壤土中的农药,然后用气相色谱串联质谱法(GC-MS/MS)进行测定。十种农药是根据文献综述中报道的存在于欧盟土壤中的化合物选择的。萃取是使用 SPME LC-Tips 进行的,这是一种新的 SPME 配置,其涂覆纤维附着在一次性且易于处理的微量移液管尖端上,该尖端浸入到通过向土壤样品中添加水溶液制成的土壤浆料中。通过 Plackett-Burman 设计评估了十个实验参数,之后分别优化了萃取时间和水溶液中有机溶剂的百分比。在整个工作中,同时评估了两种纤维化学性质(PDMS/DVB 和 C)。在最终方法中,通过向 2 克土壤中添加水溶液(6%甲醇 v/v)来制备浆料样品。纤维进行调节,然后插入样品中,用磁棒搅拌进行萃取。然后,分析物解吸到 100µL 甲醇中。在添加分析物保护剂(乙基甘油、戊二酸内酯和山梨醇)后,将提取物注入 GC-MS/MS 系统。同位素标记的戊唑醇被用作内标。通过用浓度为 0.1-50µg/kg 的分析物对土壤进行加标提取来进行校准。PDMS/DVB 的线性校准的决定系数在 0.94-0.98 之间,C 的决定系数在 0.92-0.99 之间。PDMS/DVB 的检测限范围在 0.01-10µg/kg 之间,C 的检测限范围在 0.1-10µg/kg 之间。总的来说,C 在分析性能上优于 PDMS/DVB,但需要更长的萃取时间(120 分钟与 PDMS/DVB 的 75 分钟相比)。该方法允许自动化,并且产生低残留的有毒废物,有可能作为一种更环保和更简单的替代方案引入到目前使用的样品制备方法中。

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