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同位素稀释-液相色谱/串联质谱法准确测定鸡肉中的四种四环素残留。

Accurate determination of four tetracycline residues in chicken meat by isotope dilution-liquid chromatography/tandem mass spectrometry.

机构信息

Organic Metrology Group, Division of Chemical and Biological Metrology, Korea Research Institute of Standards and Science, Daejeon 34113, South Korea; Department of Bio-Analytical Science, University of Science and Technology, Daejeon 34113, South Korea; Reference Materials Lab, National Institute of Standards, Tersa St, Haram, P. O. Box: 136, Giza 12211, Egypt.

Organic Metrology Group, Division of Chemical and Biological Metrology, Korea Research Institute of Standards and Science, Daejeon 34113, South Korea; Department of Bio-Analytical Science, University of Science and Technology, Daejeon 34113, South Korea; National Metrology Institute of Ethiopia, Addis Ababa, P. O. Box: 5722, Ethiopia.

出版信息

J Chromatogr A. 2023 Feb 22;1691:463818. doi: 10.1016/j.chroma.2023.463818. Epub 2023 Jan 24.

Abstract

An analytical method based on isotope dilution-liquid chromatography-tandem mass spectrometry (ID-LC‒MS/MS) was developed to accurately determine four representative tetracyclines (tetracycline, chlortetracycline, doxycycline, and oxytetracycline) in chicken meat. Tetracyclines are known to have a great tendency for epimerization and keto-enol tautomerism, which often provoke major challenges in their determination. Since this isomerization was found to be unavoidable during the whole chain of the current analysis, the total content (µg kg) of individual tetracycline was quantified as a sum of each parent compound and its respective isomeric forms. Using this approach in combination with IDMS analysis, more consistent, accurate, and reproducible measurement results for the four tetracyclines in chicken meat were acquired. LC-MS/MS conditions and sample preparation processes were comprehensively optimized to minimize the chelating effect of tetracyclines and possible co-extracted interferences. Details of the sample preparation scheme, LC‒MS/MS detection, calculation equation, and method validation are described in this article. The method provided very good accuracy (97.7-102.6%) for all analytes across the concentration range of 10-200 µg kg, with relative standard deviations for intra-day and inter-day precision of less than 4%. The limits of quantification were below 0.2 µg kg, demonstrating the high sensitivity of the method. Furthermore, the measurement uncertainty was generally below 5.5%. Hence, the established method exhibits high-order metrological quality with superior performance over various existing methodologies. Moreover, this method can provide references for general food testing laboratories close to and far below the established maximum residue limits (100 µg kg) for animal muscle tissues.

摘要

建立了一种基于同位素稀释-液相色谱-串联质谱法(ID-LC-MS/MS)的分析方法,用于准确测定鸡肉中四种代表性四环素(四环素、金霉素、强力霉素和土霉素)。众所周知,四环素具有很大的差向异构化和酮-烯醇互变异构倾向,这常常给它们的测定带来很大的挑战。由于在当前分析的整个过程中发现这种异构化是不可避免的,因此将单个四环素的总含量(µg kg)定量为每个母体化合物及其各自的差向异构体形式的总和。使用这种方法结合 IDMS 分析,可以获得更一致、准确和可重复的鸡肉中四种四环素的测量结果。本文详细描述了 LC-MS/MS 条件和样品制备过程的综合优化,以最大限度地减少四环素的螯合效应和可能存在的共提取干扰。该方法提供了非常好的准确度(100%),所有分析物在 10-200 µg kg 的浓度范围内,日内和日间精密度的相对标准偏差均小于 4%。定量限低于 0.2 µg kg,表明方法具有高灵敏度。此外,测量不确定度通常低于 5.5%。因此,该方法具有较高的计量质量等级,优于各种现有方法的性能。此外,该方法可为接近和远低于动物肌肉组织规定的最大残留限量(100 µg kg)的一般食品检测实验室提供参考。

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