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首页> 外文期刊>Bulletin of the Korean Chemical Society >Exact Matrix-matching Calibration by Standard Addition-Isotope Dilution-Liquid Chromatography/Mass Spectrometry for the Accurate Determination of Chloramphenicol in Infant Formula
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Exact Matrix-matching Calibration by Standard Addition-Isotope Dilution-Liquid Chromatography/Mass Spectrometry for the Accurate Determination of Chloramphenicol in Infant Formula

机译:通过标准添加 - 同位素稀释 - 液相色谱/质谱法的精确矩阵匹配校准,用于精确测定婴儿配方中氯霉素

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摘要

We consistently observed a bias in the results for determination of chloramphenicol (CAP) in infant formula by isotope dilution-liquid chromatography/mass spectrometry (ID-LC/MS). Various matrix interferences from infant formula eventually can result in bias during the ID-LC/MS analysis. We tried to optimize LC conditions to minimize matrix effects by separating significant matrix interferences from the analyte and the internal standard, but some level of bias remained. To eliminate the bias due to the matrix effects, we used a standard addition-isotope dilution-liquid chromatography/mass spectrometry (SA-ID-LC/MS) method for CAP analysis. In the SA-ID-LC/MS method, standard addition techniques were combined with IDMS for exact matrix matching while keeping the isotope dilution techniques as a tool for accurate correction of recovery in sample preparation processes. The method provided accurate analytical results for target analyte in the range of 1 mu g/kg with a relative expanded uncertainty of 3%.
机译:我们在同位素稀释 - 液相色谱/质谱(ID-LC / MS)中始终如一地观察到婴儿配方幼儿配方丙氨酸(帽)的结果。来自婴儿公式的各种基质干扰最终可能导致ID-LC / MS分析期间偏置。我们试图通过分析物和内标分离显着的矩阵干扰来优化LC条件以最小化矩阵效应,但仍然存在一定程度的偏差。为了消除由于基质效应引起的偏差,我们使用了标准添加同位素稀释 - 液相色谱/质谱法用于帽分析。在SA-ID-LC / MS方法中,将标准添加技术与IDMS结合以进行精确的矩阵匹配,同时将同位素稀释技术保持为用于精确校正样品制备方法中的恢复的工具。该方法为靶分析物提供了准确的分析结果,其范围为1μg/ kg,具有3%的相对膨胀不确定度。

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