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采用 96 孔板自动萃取和高效液相色谱-串联质谱法对人尿液中乙酰甲胺磷、甲胺磷、氧乐果、乐果、乙撑硫脲和丙撑硫脲进行高通量样品制备及定量分析。

High-throughput sample preparation for the quantitation of acephate, methamidophos, omethoate, dimethoate, ethylenethiourea, and propylenethiourea in human urine using 96-well-plate automated extraction and high-performance liquid chromatography-tandem mass spectrometry.

机构信息

Centers for Disease Control and Prevention, Atlanta, GA 30341, USA.

出版信息

Arch Environ Contam Toxicol. 2011 Jul;61(1):59-67. doi: 10.1007/s00244-010-9593-3. Epub 2010 Sep 28.

Abstract

Acephate, methamidophos, o-methoate, and dimethoate are organophosphorus pesticides, and ethylenethiouria and propylenethiourea are two metabolites from the bisdithiocarbamate fungicide family. They are some of the most widely used pesticides and fungicides in agriculture both domestically and abroad. The existing high-performance liquid chromatography (HPLC)-tandem mass spectrometry (MS/MS) method for the measurement of these compounds in human urine was improved by using a 96-well plate format sample preparation; the use of HPLC-MS/MS was comparable with a concentration range of 0.125 to 50 ng/ml. Deuterium-labeled acephate, ethylenethiouria, and methamidophos were used as internal standards. The sample preparation procedure, in the 96-well format with a 0.8-ml urine sample size, uses lyophilization of samples, followed by extraction with dichloromethane. The analytes were chromatographed on a Zorbax SB-C3 (4.6 × 150 mm, 5.0-μm) column with gradient elution by using 0.1% formic acid in aqueous solution (solvent A) and 0.1% formic acid in methanol (solvent B) mobile phase at a flow rate of 1 ml/min. Quantitative analysis was performed by atmospheric pressure chemical ionization source in positive ion mode using multiple-reaction monitoring of the precursor-to-product ion pairs for the analytes on a TSQ Quantum Ultra HPLC-MS/MS. Repeated analyses of urine samples spiked with high (15 ng/ml), medium (5 ng/ml), and low (1 ng/ml) concentrations of the analytes gave relative SDs of <13%. The limits of detection were in the range of 0.004-0.01 ng/ml. The method also has high accuracy, high precision, and excellent extraction recovery. Furthermore, the improved sample preparation method decreased the cost and labor required while effectively doubling the analytic throughput with minimal matrix effect.

摘要

乙酰甲胺磷、甲胺磷、氧乐果和乐果是有机磷农药,乙撑硫脲和丙撑硫脲是双二硫代氨基甲酸盐类杀菌剂家族的两种代谢物。它们是国内外农业中使用最广泛的农药和杀菌剂之一。现有的高效液相色谱(HPLC)-串联质谱(MS/MS)法用于测量人尿中的这些化合物,通过使用 96 孔板格式的样品制备方法进行了改进;HPLC-MS/MS 的使用与浓度范围为 0.125 至 50ng/ml 相当。使用氘标记的乙酰甲胺磷、乙撑硫脲和甲胺磷作为内标。在 96 孔格式中,使用 0.8ml 尿液样品,采用样品冷冻干燥,然后用二氯甲烷提取。使用 Zorbax SB-C3(4.6×150mm,5.0-μm)柱,以 0.1%甲酸水溶液(溶剂 A)和 0.1%甲酸甲醇(溶剂 B)为流动相进行梯度洗脱,流速为 1ml/min。通过大气压化学电离源在正离子模式下,对分析物的前体-产物离子对进行多反应监测,在 TSQ Quantum Ultra HPLC-MS/MS 上进行定量分析。对高(15ng/ml)、中(5ng/ml)和低(1ng/ml)浓度的分析物尿液样品进行重复分析,相对标准偏差(SD)<13%。检测限范围为 0.004-0.01ng/ml。该方法还具有高准确性、高精密度和良好的提取回收率。此外,改进的样品制备方法降低了成本和劳动力需求,同时有效地将分析通量提高了一倍,并且基质效应最小。

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