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作 者:莫瑾[1] 龚强[1] 周慧平[1] 白雪[1] 谭建锡[1] 彭梓[1] 黄迎波[1]
机构地区:[1]湖南出入境检验检疫局检验检疫技术中心,国家食品安全检测重点实验室,食品安全科学技术湖南省重点实验室,长沙410004
出 处:《食品安全质量检测学报》2016年第1期182-187,共6页Journal of Food Safety and Quality
基 金:国家质检总局项目(2010IK133)~~
摘 要:目的建立高效液相色谱-串联质谱联用技术检测茶叶中赭曲霉毒素A(OTA)的方法。方法用甲醇-2%Na HCO3溶液(60:40,V:V)提取样品中的赭曲霉毒素A,采用免疫亲和柱对茶叶中的赭曲霉毒素A净化,使用甲醇-5 mmol/L乙酸铵(含0.1%乙酸)为流动相,检测赭曲霉毒素A,采用正离子模式。结果本方法中赭曲霉毒素A在0.5~10 ng/m L质量浓度范围内具有良好的线性关系(r=0.996),回收率在83.6%~92.5%之间,相对标准偏差在6.5%~9.1%之间,检出限为0.1μg/kg。结论该方法准确性好、灵敏度高,适用于茶叶样品的检测。Objective To establish a method for the determination of ochratoxin A (OTA) in tea by high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). Methods Samples were extracted by methanol-2% sodium bicarbonate solution (60:40, V:V), followed by clean-up on OchraTest affinity cartridge using methanol-5 mmol/L ammonium acetate solution in the presence of 0.1% formic acid as the mobile phase. OTA was detected in positive ion mode. Results A good linearity (r=0.996) was achieved for the target compounds in the range of 0.5-10 ng/mL. The recoveries of ochratoxin A in 4 tea samples were varied from 83.6% to 92.5% (n = 5) with the relative standard deviations from 6.5% to 9.1%. The limit of detection was 0.1μg/kg. Conclusion The method is accurate and sensitive, and suitable for the determination of ochratoxin A in tea samples.
关 键 词:高效液相色谱-串联质谱法 赭曲霉毒素A 免疫亲和柱 茶叶
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