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作 者:陈燕秋 林浩 肖全伟 宋娟 刘川 戴琴 CHEN Yanqiu;LIN Hao;XIAO Quanwei;SONG Juan;LIU Chuan;DAI Qin(Chengdu Institute of Food Inspection,Chengdu 611130,China;Key Laboratory of Chemical Metrologyand Applications on Nutrition and Healthfor State Market Regulation,Beijing 100029,China;Irradiation Preservation Technology Key Laboratory of Sichuan Province,Sichuan Institute of Atomic Energy,Chengdu 610101,China)
机构地区:[1]成都市食品检验研究院,四川成都611130 [2]国家市场监管重点实验室(营养与健康化学计量及应用),北京100029 [3]四川省原子能研究院,辐照保藏四川省重点实验室,四川成都610101
出 处:《食品科学》2024年第12期285-291,共7页Food Science
基 金:“十四五”国家重点研发计划重点专项(2022YFF0710405)。
摘 要:建立同时快速测定牛乳中氟吡呋喃酮及其代谢物6-氯烟酸和二氟乙酸的超高效液相色谱-串联质谱分析方法。牛乳样品前处理采用简单高效的分散式固相萃取法(QuEChERS)净化,并对净化策略进行了评估,经改进的QuEChERS处理后,以乙腈-水(含0.1%甲酸)为流动相在Shim-pack-GIST C_(18)色谱柱上进行分离,多反应监测模式测定,基质标准曲线外标法定量。在优化的条件下,氟吡呋喃酮、6-氯烟酸、二氟乙酸分别在0.005~0.5、0.005~0.5、0.025~2.5 mg/L质量浓度范围内线性关系良好(R^(2)>0.996),在3个添加水平条件下的平均加标回收率为70.2%~97.6%,相对标准偏差为3.6%~5.3%,检出限为0.01~0.05 mg/kg。该方法操作简单、准确度和灵敏度高、重现性好,定量限远低于国家规定的最高限量,适用于大批量牛乳样品中氟吡呋喃酮及其代谢物残留的准确测定,实验结果为监管提供了可靠的技术支撑。A rapid method was developed for the simultaneous determination of flupyradifurone and its metabolites 6-chloronicotinic acid and difluoroacetic acid in milk using ultra-high performance liquid chromatography-tandem mass spectrometry(UPLC-MS/MS).A simple and efficient dispersive solid phase extraction method was used to purify milk samples,and the purification strategy was evaluated.After improved quick,easy,cheap,effective,rugged and safe(QuEChERS)treatment,0.1%formic acidin acetonitrilewas used as the mobile phase for chromatographicseparation on a Shim-pack-GIST C_(18) column(100mm×2.1mm,1.7μm),and the detection was performed in themultiple reaction monitoring(MRM)mode.Theexternal standard methodwith matrix standard curveswas used for quantification.The results showed that under the optimal conditions,good linearity(linear correlation coefficient greater than0.996)was observed for flurofuranone,6-chloronicotinic acid and difluoroacetic acid in the concentration ranges of 0.005–0.5,0.005–0.5 and 0.025–2.5mg/L,respectively.The average recoveries of flupyradifurone and its metabolitesat three spiked concentrations varied from 70.2%to 97.6%,with relative standard deviations(RSDs)between 3.6%and 5.3%,and the limits of detection(LODs)ranged from 0.01 to 0.05 mg/kg,much lower than the national maximum residue limits.This method was characterized by high accuracy,highsensitivity,and good reproducibility.It is,therefore,suitable for large batches of milk samples,and can provide reliable technical support for the management of the pesticide flupyradifurone.
关 键 词:超高效液相色谱-串联质谱 QUECHERS 氟吡呋喃酮 代谢物 牛乳
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