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作 者:张利强[1] 邢淑莲[2] 林丽云 林玲[1] 叶剑芝[1] 杨春亮[1] ZHANG Li-qiang;XING Shu-lian;LIN Li-yun;LIN Ling;YE Jian-zhi;YANG Chun-liang(Agricultural Products Processing Quality and Safety Risk Assessment Laboratory,Ministry of Agriculture and Rural Affairs,Agricultural Products Processing Research Institute,Chinese Academy of Tropical Agricultural Sciences, Zhanjiang 524002,China;Zhanjiang Experimental Station,Chinese Academy of Tropical Agricultural Sciences,Zhanjiang 524002,China)
机构地区:[1]中国热带农业科学院农产品加工研究所,农业农村部农产品加工质量安全风险评估实验室(湛江),广东湛江524002 [2]中国热带农业科学院湛江实验站,广东湛江524002
出 处:《分析测试学报》2018年第8期945-949,共5页Journal of Instrumental Analysis
基 金:海南省自然科学基金资助项目(20162034);国家农产品质量安全风险评估重大专项(GJFP2017011)
摘 要:建立了固相萃取/高效液相色谱测定火龙果中手性苯醚甲环唑的方法。火龙果样品经乙腈提取,石墨化炭黑/氨基固相萃取柱净化后进行测定。实验考察了不同手性色谱柱、流动相组成、流速及进样体积对分离的影响,通过优化分离成功拆分了苯醚甲环唑对映体。优化的色谱条件为:Chrialcel IF-3手性柱为色谱柱,正己烷-乙醇(92∶8,体积比)为流动相,流速为1.0 m L/min,进样量为60μL。在上述条件下,4个对映体基本完全分离,分析时间不超过35 min。单个对映体在0.10~10 mg/L范围内呈良好的线性关系,检出限为0.025 mg/L。分别添加0.4、2.8 mg/kg两个水平的外消旋苯醚甲环唑,测得4个对映体的平均回收率分别为83.7%~99.3%和86.4%~91.6%,相对标准偏差分别为1.3%~7.2%和1.4%~3.1%。该方法的分离时间较短,分离效果好,灵敏度高,适用于火龙果等水果中手性农药苯醚甲环唑含量的测定。A method was established for the determination of chiral difenoconazole in dragon fruit by solid-phase extraction coupled with high performance liquid chromatography.The dragon fruit samples were extracted with acetonitrile,and purified with carbon black/amino solid phase extraction column.Effects of different chiral columns,mobile phase compositions,flow rates and injection volumes on chiral separation were investigated.The optimized chromatographic conditions were as follows:the chromatographic column:IF-3 chiral column,mobile phase:n-hexane-ethanol(92∶8 by volume),injection volume:60μL,flow rate:1.0 mL/min.Under the optimized conditions,the four difenoconazole enantiomers were basically achieved baseline separation,and the analysis time was less than 35 min.There existed a good linearity for each enantiomer in the range of 0.10-10 mg/L,with a detection limit of 0.025 mg/L.The average recoveries for the chiral difenoconazole in dragon fruit at two spiked levels of 0.4 mg/kg and 2.8 mg/kg were in the ranges of 83.7%-99.3%and 86.4%-91.6%,with their RSDs of 1.3%-7.2%and 1.4%-3.1%,respectively.The developed method is rapid,accurate and sensitive,and is applicable for the determination of chiral difenoconazole residues in dragon fruit,etc.
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