Natural Products Chemistry Laboratory, Biotechnology Research Institute, Chonnam National University, 77 Yongbong-ro, Buk-gu, Gwangju 500-757, Republic of Korea.
Food Chem. 2013 Jun 15;138(4):2306-11. doi: 10.1016/j.foodchem.2012.12.029. Epub 2013 Jan 7.
This paper describes a comparison of the properties of the three versions of the QuEChERS method (quick, easy, cheap, effective, rugged and safe) - the original (unbuffered), acetate-buffered, and citrate-buffered methods - for the determination of fenobucarb residues in beef muscles via liquid chromatography-electrospray ionisation tandem mass spectrometry (LC-ESI(+)-MS/MS). The recovery results were good for all the versions; however, the acetate-buffered version gave higher and more consistent recoveries for fenobucarb than the other versions. Performance characteristics, such as linearity, accuracy, and precision were determined. Matrix-matched standard calibration was used for quantification, obtaining recoveries in the range of 83.7-93.4% with relative standard deviations of <5%, at two spiking levels: 10 and 40 μg/kg. The limits of detection (LOD) and quantification (LOQ) were estimated to be 1.5 and 5 μg/kg, respectively. Finally, the method was applied to the analysis of 15 market samples, and no residues were found over the limit of quantification. The method developed was found able to determine the analyte with satisfactory intensity and accuracy.
本文描述了三种 QuEChERS 方法(快速、简单、廉价、有效、耐用和安全)——原始(非缓冲)、乙酸盐缓冲和柠檬酸盐缓冲方法——在通过液相色谱-电喷雾离子化串联质谱(LC-ESI(+)-MS/MS)测定牛肉肌肉中 Fenobucarb 残留量方面的性能比较。所有版本的回收率结果都很好;然而,与其他版本相比,乙酸盐缓冲版本对 Fenobucarb 的回收率更高且更一致。测定了性能特征,如线性、准确性和精密度。采用基质匹配标准校准进行定量,在两个加标水平(10 和 40 μg/kg)下,回收率在 83.7-93.4%范围内,相对标准偏差<5%。检测限(LOD)和定量限(LOQ)分别估计为 1.5 和 5 μg/kg。最后,该方法应用于 15 个市场样品的分析,未发现超过定量限的残留。所开发的方法能够以令人满意的强度和准确性来测定分析物。