李鹏,刘凯丽,杨欣,赵云峰,吴永宁.高压液相色谱-线性离子阱串联质谱法测定红葡萄酒中多菌灵和甲基硫菌灵[J].食品安全质量检测学报,2013,4(1):89-93
高压液相色谱-线性离子阱串联质谱法测定红葡萄酒中多菌灵和甲基硫菌灵
Determination of carbendazim and thiophanate-methyl in red wine by high pressure liquid chromatography-linear ion trap mass spectrometry
投稿时间:2012-11-08  修订日期:2012-12-27
DOI:
中文关键词:  高压液相色谱-线性离子阱质谱法(HPLC-LIT-MS)  红葡萄酒  多菌灵  甲基硫菌灵
英文关键词:high pressure liquid chromatography-linear ion trap mass spectrometry (HPLC-LIT-MS)  red wine  carbendazim  thiophanate-methyl
基金项目:十二五国家科技支撑计划(2011BAK10B06)
作者单位
李鹏 国家食品安全风险评估中心 
刘凯丽 北京市丰台区动物卫生监督所 
杨欣 国家食品安全风险评估中心 
赵云峰 国家食品安全风险评估中心; 卫生部食品安全风险评估重点实验室 
吴永宁 国家食品安全风险评估中心; 卫生部食品安全风险评估重点实验室 
AuthorInstitution
LI Peng China National Center for Food Safety Risk Assessment 
LIU Kai-Li Beijing Fengtai District Animal Health Inspection 
YANG Xin China National Center for Food Safety Risk Assessment 
ZHAO Yun-Feng China National Center for Food Safety Risk Assessment; Key Lab of Food Safety Risk Assessment, Ministry of Health 
WU Yong-Ning China National Center for Food Safety Risk Assessment; Key Lab of Food Safety Risk Assessment, Ministry of Health 
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中文摘要:
      目的 建立红葡萄酒中多菌灵和甲基硫菌灵残留的高压液相色谱-串联线性离子阱质谱(HPLC-LIT-MS/MS)检测方法。方法 样品经过乙腈提取, 在梯度洗脱程序下经CAPCELL PAK CR 1:20色谱柱分离后, 采用HPLC-LIT-MS/MS, 在二级质谱选择反应监测(SRM)模式进行测定。结果 红葡萄酒中多菌灵和甲基硫菌灵添加水平为10、20、50 μg/L时, 平均回收率分别为82.5%~103.1%和93.7%~115.2%。检出限(LODs)分别为0.063 μg/L和0.019 μg/L, 定量限(LOQs)分别为0.125 μg/L和0.075 μg/L。结论 该方法快速简便, 灵敏度高, 准确度和精密度均满足痕量分析要求。
英文摘要:
      Objective To develop a method of high pressure liquid chromatography-linear ion trap mass spectrometry (HPLC-LIT-MS) for the determination of carbendazim and thiophanate-methyl in red wine. Methods Samples were ultrasonically extracted with acetonitrile, separated on a CAPCELL PAK CR 1:20 column with gradient elution and the mass spectrometric acquisition was carried out under the mode of selected reaction monitoring (SRM). Results The average recoveries of carbendazim and thiophanate-methyl in red wine at 10, 20 μg/L and 50 μg/L were 82.5%~103.1% and 93.7%~115.2%, respectively. The limits of detection (LODs) were 0.063 μg/L and 0.019 μg/L, and the limits of quantification (LOQs) were 0.125 μg/L and 0.075 μg/L. Conclusion The established method is fast, simple, selective, precise and accurate, and it is suitable for quantitative and qualitative detection of carbendazim and thiophanate-methyl in red wine.
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