Furusawa Naoto
Graduate School of Human Life Science, Osaka City University, Osaka 558-8585, Japan.
J Chromatogr A. 2007 Nov 16;1172(1):92-5. doi: 10.1016/j.chroma.2007.08.040. Epub 2007 Aug 21.
A quick and cost-effective technique of sample preparation followed by a reversed-phase high performance liquid chromatography under "organic solvent-free" (=100% aqueous) conditions for the simultaneous quantifying of sulfadimethoxine (SDM) and its metabolites, 6-hydroxy SDM (6-OH) and N(4)-acetyl SDM (N(4)-Ac), in chicken muscle is presented. Analysis by HPLC with photo-diode array detector was performed using a short C1 column with an isocratic 0.04 mol/l citric acid mobile phase. The method was validated by the analyses of spiked chicken muscle samples, resulting recoveries (> or =84%; relative standard deviations < or =6%), analytical total time (<1/2 h/sample, where a batch of 12 samples in 4 h), and limits of quantitation (< or =0.1 microg/g). The decision limits and detection capability were 0.019-0.106 and 0.054-0.112 microg/g, respectively. No organic solvents were used at all.
本文介绍了一种快速且经济高效的样品制备技术,随后在“无有机溶剂”(即100%水性)条件下采用反相高效液相色谱法,用于同时定量测定鸡肉中磺胺二甲氧嘧啶(SDM)及其代谢产物6-羟基磺胺二甲氧嘧啶(6-OH)和N(4)-乙酰磺胺二甲氧嘧啶(N(4)-Ac)。使用配备光电二极管阵列检测器的高效液相色谱仪,采用短C1柱和0.04 mol/l柠檬酸等度流动相进行分析。通过对加标鸡肉样品的分析验证了该方法,回收率(≥84%)、相对标准偏差(≤6%)、分析总时间(<1/2小时/样品,4小时可分析一批12个样品)和定量限(≤0.1 μg/g)均符合要求。决策限和检测能力分别为0.019 - 0.106和0.054 - 0.112 μg/g。整个过程完全未使用有机溶剂。