Ghosson Hikmat, Raviglione Delphine, Salvia Marie-Virginie, Bertrand Cédric
PSL Université Paris: EPHE-UPVD-CNRS, USR 3278 CRIOBE, Université de Perpignan, 52 Avenue Paul Alduy, 66860, Perpignan Cedex, France; UFR Sciences Exactes et Expérimentales, Université de Perpignan Via Domitia, 52 Avenue Paul Alduy, 66860, Perpignan Cedex, France.
PSL Université Paris: EPHE-UPVD-CNRS, USR 3278 CRIOBE, Université de Perpignan, 52 Avenue Paul Alduy, 66860, Perpignan Cedex, France; UFR Sciences Exactes et Expérimentales, Université de Perpignan Via Domitia, 52 Avenue Paul Alduy, 66860, Perpignan Cedex, France.
Anal Chim Acta. 2020 Oct 16;1134:58-74. doi: 10.1016/j.aca.2020.08.016. Epub 2020 Aug 20.
This work introduces a novel online Headspace-Solid Phase Microextraction-Gas Chromatography-Mass Spectrometry-based untargeted metabolomics approach, suggested as an alternative tool to study the environmental fate of volatile xenometabolites in emerging complex biopesticides, e.g. the Myrica gale methanolic extract herbicide containing several unknown metabolites. A "living" microcosm sample was designed for non-destructive analysis by a 35-min HS-SPME automated extraction and a 36-min GC-MS run. A 38-day kinetics study was then applied on two groups of soil samples: control and spiked. Statistical tools were used for the comparative kinetics study. The Principal Component Analysis revealed and explained the evolution and the dissipation of the herbicide volatile xenometabolome over time. The time-series Heatmap and Multivariate Empirical Bayes Analysis of Variance allowed the prioritization of 101 relevant compounds including 22 degradation by-products. Out of them, 96 xenometabolites were putatively identified. They included 63 compounds that are identified as herbicide components for the first time. The Orthogonal Projections to Latent Structures Discriminant Analysis and its Cross-Validation test were used to assess the total dissipation of the herbicide volatile residues and method detection limit. The reproducibility of the method was also assessed. The highest inter-samples (n = 3) Peak Area RSD was 7.75 %. The highest inter-samples (n = 3) and inter-days (n = 8) Retention Time SD were 0.43 sec and 3.44 sec, respectively. The work presents a green, non-laborious and high-throughput approach. It required a small number of environmental samples (6 microcosms) that were analyzed 8 times and were not destroyed during the study.
本研究介绍了一种基于顶空-固相微萃取-气相色谱-质谱联用的新型在线非靶向代谢组学方法,该方法被建议作为一种替代工具,用于研究新型复杂生物农药中挥发性异源代谢物的环境归宿,例如含有多种未知代谢物的杨梅甲醇提取物除草剂。通过35分钟的顶空固相微萃取自动萃取和36分钟的气相色谱-质谱分析,设计了一个“活体”微观世界样本用于非破坏性分析。然后对两组土壤样本(对照组和加标组)进行了为期38天的动力学研究。使用统计工具进行比较动力学研究。主成分分析揭示并解释了除草剂挥发性异源代谢组随时间的演变和消散情况。时间序列热图和多变量经验贝叶斯方差分析对101种相关化合物进行了优先级排序,其中包括22种降解副产物。其中,96种异源代谢物被初步鉴定。它们包括63种首次被鉴定为除草剂成分的化合物。使用正交投影到潜在结构判别分析及其交叉验证测试来评估除草剂挥发性残留的总消散情况和方法检测限。还评估了该方法的重现性。最高的样本间(n = 3)峰面积相对标准偏差为7.75%。最高的样本间(n = 3)和日间(n = 8)保留时间标准偏差分别为0.43秒和3.44秒。这项工作提出了一种绿色、省力且高通量的方法。它只需要少量环境样本(6个微观世界样本),这些样本被分析了8次,且在研究过程中未被破坏。