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液相色谱-串联质谱法检测调味品中碱性橙2的残留量 被引量:4

Determination of basic orange Ⅱ residues in condiment by liquid chromatography-tandem mass spectrometry
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摘要 目的建立液相色谱-电喷雾质谱法(liquid chromatography-tandem mass spectrometry, UPLC–MS/MS)检测调味品中碱性橙2的分析方法。方法样品经酸化乙腈提取,正己烷去脂后,经固相萃取小柱净化,氮气吹干进行富集后,用乙腈溶解,再采用液相色谱-电喷雾质谱进行检测,以正离子多反应监测模式测定,外标法定量。结果碱性橙2的线性范围为0.2~20 ng/mL,线性方程为Y=0.0993X-0.0106 (r=0.9999),加标回收率为90.0%~110.0%,相对标准偏差小于10.0%(n=6);方法检出限为1μg/kg,定量限为3μg/kg。结论该方法快速、准确、灵敏,适合用于食品中碱性橙2的确证检测。 Objective To establish a method for the deternamiton of basic orange Ⅱ residues in condiment by liquid chromatography-tandem mass spectrometry. Methods The sample was extracted by acidizing acetonitrile, deacidized by n-hexane, and purified by solid-phase extraction and enriched by nitrogen blow-dry. Then it was dissolved by acetonitrile and detected by liquid chromatography-mass spectrometry(electronic spray ion) with the cationic multiple reaction monitoring model, and quantified by external standard method. Results Basic orange Ⅱhad good linear relationships in the range of 0.2-20 ng/mL, and the linear equation was Y=0.0993 X-0.0106(r=0.9999). The average recoveries at 3 concentration levels were between 90% and 110%, and the relative standard deviations(RSDs) were less than 10.0%(n=6). The limits of detection(LODs) were 1 μg/kg and the limits of quantitation were 3 μg/kg. Conclusion This method is rapid, accurate and sensitive, which is suitable for detecting basic orange Ⅱ in condiment samples.
作者 李彦博 孙晓娟 高广慧 LI Yan-Bo;SUN Xiao-Juan;GAO Guang-Hui(Liaoning Institute for Food Control,Shenyang 110015,China)
出处 《食品安全质量检测学报》 CAS 2018年第19期5119-5122,共4页 Journal of Food Safety and Quality
关键词 碱性橙2 液相色谱串联质谱法 固相萃取 调味品 残留量 basic orange Ⅱ liquid chromatography-tandem mass spectrometry solid phase extraction condiment residues
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