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通过DART-MS/MS结合微固相萃取和双重碎裂对丁草胺进行高通量定量分析,以提高选择性和灵敏度。

High-throughput quantification of butachlor by DART-MS/MS coupled with micro-solid-phase extraction and dual fragmentation to enhance selectivity and sensitivity.

作者信息

Li Huaqiang, Wu Feifei, Ding Yuxian, Long Guozhou, Yin Lei

机构信息

Guangdong Provincial Key Laboratory for Green Agricultural Production and Intelligent Equipment, College of Biological and Food Engineering, Guangdong University of Petrochemical Technology, Maoming, 525000, Guangdong, China.

Guangdong Guozhou Traditional Chinese Medicine Co., Ltd, Maoming, 525000, Guangdong, China.

出版信息

Anal Bioanal Chem. 2025 Aug;417(20):4605-4615. doi: 10.1007/s00216-025-05975-0. Epub 2025 Jun 27.

Abstract

A novel and rapid analytical assay based on direct analysis in real-time tandem mass spectrometry (DART-MS/MS) technology was established for quantification of butachlor in this study. The assay incorporated micro-solid-phase extraction (μ-SPE) for sample pretreatment, with acetochlor as an internal standard. Quantification was achieved via transitions from [M + H] precursor ions to primary and secondary fragment ions at m/z 312.1 → 238.0 → 162.1 (butachlor) and 270.1 → 224.1 → 148.0 (acetochlor). This chromatography-free approach eliminated reliance on mobile phases and chromatographic instrumentation, significantly improving analytical throughput (0.4 min/sample) while reducing environmental impact. Method validation demonstrated linearity over 0.5-100 ng/mL (R > 0.995), with intra-/inter-day precision < 13.1% and accuracy ranging from -6.00% to 11.0%. The assay was used to evaluate the cellular uptake kinetics of butachlor in MCF-7 cells. These findings underscore the utility of DART-MS/MS assay for rapid environmental and toxicological assessments while highlighting potential safety concerns associated with butachlor exposure. The integration of DART-MS/MS with μ-SPE offers a sustainable alternative to conventional bioanalytical workflows, combining speed, sensitivity, and reduced chemical consumption for ecotoxicological studies.

摘要

本研究建立了一种基于实时串联质谱直接分析(DART-MS/MS)技术的新型快速分析方法,用于定量分析丁草胺。该方法采用微固相萃取(μ-SPE)进行样品预处理,以乙草胺作为内标。通过监测质荷比为312.1→238.0→162.1(丁草胺)和270.1→224.1→148.0(乙草胺)的从[M + H]前体离子到一级和二级碎片离子的跃迁来实现定量分析。这种无需色谱的方法消除了对流动相和色谱仪器的依赖,显著提高了分析通量(0.4分钟/样品),同时减少了对环境的影响。方法验证表明,在0.5 - 100 ng/mL范围内具有线性关系(R > 0.995),日内/日间精密度< 13.1%,准确度在-6.00%至11.0%之间。该方法用于评估丁草胺在MCF-7细胞中的细胞摄取动力学。这些发现强调了DART-MS/MS分析方法在快速环境和毒理学评估中的实用性,同时突出了与丁草胺暴露相关的潜在安全问题。DART-MS/MS与μ-SPE的结合为传统生物分析工作流程提供了一种可持续的替代方案,结合了速度、灵敏度和减少化学消耗,适用于生态毒理学研究。

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