检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:郑佳 郗存显[3] 曹淑瑞[3] 王国民[3] 唐柏彬[3] 王智 母昭德[1,2] Zheng Jia;Xi Cunxian;Cao Shurui;Wang Guomin;Tang Bobin;Wang Zhi;Mu Zhaode(College of Pharmacy ,Chongqing Medical University , Chongqing 400016, China;Chongqing Entry -Exit Inspection and Quarantine Bureau Chongqing Engineering Technology Research Center of Import and Export Food Safety ,Chongqing 400020,China;Chongqing Key Laboratory of Biochemistry and Molecular Pharmacology, Chongqing 400016, China)
机构地区:[1]重庆医科大学药学院,重庆400016 [2]重庆市生物化学与分子药理学重点实验室,重庆400016 [3]重庆出入境检验检疫局重庆市进出口食品安全工程技术研究中心,重庆400020
出 处:《色谱》2017年第12期1257-1265,共9页Chinese Journal of Chromatography
基 金:国家质量监督检验检疫总局科技计划项目(2016IK296);重庆市科学技术委员会青年科学基金专项项目(cstc2014kjrc-qnrc00002)~~
摘 要:建立了QuEChERS-超高效液相色谱-串联质谱测定改善睡眠类和提高免疫力类保健食品中21种非法添加化学药物的分析方法。口服液、保健酒分别用乙腈和乙腈-水-甲酸(60∶39∶1,v/v/v)振荡提取,QuEChERS法净化;采用Acquity UPLCTMBEH C18色谱柱(50 mm×2.1 mm,1.7μm)分离,以乙腈和2 mmol/L乙酸铵溶液(含0.1%(v/v)甲酸)为流动相进行梯度洗脱;在电喷雾离子源正离子模式(ESI+)下电离,多反应监测(MRM)模式检测。结果表明,21种化学药物在1~100μg/L范围内线性关系良好,相关系数(R2)均≥0.992,检出限(LOD)为0.07~3.41μg/kg,定量限(LOQ)为0.22~11.36μg/kg。3种加标水平(10、20和100μg/kg)下,21种化学药物在口服液和保健酒中的平均加标回收率分别为61.4%~116.5%和67.4%~98.4%;相对标准偏差(RSD)分别为0.2%~13.4%和0.2%~11.8%。该法简便,灵敏性高,实用性强,可用于改善睡眠和提高免疫力类保健食品中21种非法添加化学药物的检测。A method for the simultaneous determination of21illegally added chemical drugs inimproving sleep and immunity health foods using ultra performance liquid chromatography tandem mass spectrometry(UPLC-MS/M S)was developed.Oral liquid and health wine samples were shaken with acetonitrile and acetonitrile-water-formic acid(60:39:1,v/v/v),respectively,then purified by QuEChERS method.The extracts were separated on an Acquity UPLCTM BEH C18column(50mmx2.1mm,1.7pm)with gradient elution of acetonitrile and2mmol/L ammonium acetate solution containing0.1%(v/v)formic acid as mobile phases.The electrospray ionization in positive ion mode was used for analysis in multiple reaction monitoring(MRM)mode.The results showed that the target drugs had a good linear relationship in the range of1-100pg/L with the correlation coefficients(R2)≥0.992.The limits of detection(LODs)and limits of quantification(LOQs)were0.07-3.41pg/kg and0.22-11.36pg/k g,respectively.The average recoveries of the21chemical drugs in oral liquid and health winewere in the range of61.4%-116.5%and67.4%-98.4%with the relative standard deviations(RSDs)of0.2%-13.4%and0.2%-11.8%,respectively.The developed method is sensitive andreliable.It has been successfully used for the detection of illegally added chemical drugs in real samples.
关 键 词:超高效液相色谱-串联质谱 QUECHERS 化学药物 保健食品
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.222