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采用液相色谱-离子阱三级质谱法测定橙子中丁硫克百威及其代谢物。

Determination of carbosulfan and its metabolites in oranges by liquid chromatography ion-trap triple-stage mass spectrometry.

作者信息

Soler Carla, Mañes Jordi, Picó Yolanda

机构信息

Laboratori de Bromatologia i Toxicología, Facultat de Farmàcia, Universitat de València, 46100 Burjassot, Valencia, Spain.

出版信息

J Chromatogr A. 2006 Mar 24;1109(2):228-41. doi: 10.1016/j.chroma.2006.01.026. Epub 2006 Feb 3.

Abstract

Liquid chromatography ion-trap mass spectrometry LC-MSn has been successfully applied to identify and confirm carbosulfan and seven of its metabolites in oranges after pressurized liquid extraction (PLE) with dichloromethane. Mass spectra of carbosulfan and its metabolites were investigated using multiple stages of mass spectrometry. Although interpretation of the fragmentation pathways, based on mass spectra, enables structural elucidation and identification of these compounds, the proposed fragmentation pathways and ion structures need verification by exact mass measurements. The analytical method--PLE and LC-MS3 --was validated: limits of quantification (LOQ) ranged from 0.01 to 0.07 mg kg(-1); at this level, recoveries were 55-90% with RSDs (five replicate analyses) from 8 to 19%. The degradation of carbosulfan was determined in a laboratory study carried out in mature oranges (Valencia Late) and tangerines (Clementine of Nules) already harvested. Main degradation products of carbosulfan were carbofuran, 3-hydroxycarbofuran, 3-ketocarbofuran and dibutylamine.

摘要

液相色谱-离子阱质谱联用(LC-MSn)已成功应用于通过二氯甲烷加压液体萃取(PLE)后对橙子中的丁硫克百威及其七种代谢物进行鉴定和确证。使用多级质谱研究了丁硫克百威及其代谢物的质谱。尽管基于质谱对裂解途径的解释能够对这些化合物进行结构解析和鉴定,但所提出的裂解途径和离子结构需要通过精确质量测量来验证。对分析方法——PLE和LC-MS3进行了验证:定量限(LOQ)范围为0.01至0.07 mg kg⁻¹;在此水平下,回收率为55%至90%,相对标准偏差(五次重复分析)为8%至19%。在对已收获的成熟橙子(晚熟巴伦西亚橙)和橘子(努尔斯克里曼丁橘)进行的实验室研究中测定了丁硫克百威的降解情况。丁硫克百威的主要降解产物为克百威、3-羟基克百威、3-酮基克百威和二丁胺。

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