分析化学
分析化學
분석화학
CHINESE JOURNAL OF ANALYTICAL CHEMISTRY
2015年
2期
271-276
,共6页
诸力%陈红平%周苏娟%王川丕%刘新
諸力%陳紅平%週囌娟%王川丕%劉新
제력%진홍평%주소연%왕천비%류신
茶叶%草甘膦%氨甲基膦酸%草铵膦%超高效液相色谱-串联质谱
茶葉%草甘膦%氨甲基膦痠%草銨膦%超高效液相色譜-串聯質譜
다협%초감련%안갑기련산%초안련%초고효액상색보-천련질보
Tea%Glyphosate%Aminomethyl phosphonic acid%Glufosinate%Ultra performance liquid chromatography-tandem mass spectrometry
建立了超高效液相色谱-串联质谱同时快速测定不同茶叶中草甘膦、氨甲基膦酸及草铵膦的方法。样品用0.05 mol/L NaOH提取,并以HCl调节pH值, Oasis HLB小柱净化除杂,氯甲酸-9-芴基甲酯( FMOC-Cl)柱前衍生反应后,超高效液相色谱-串联质谱法测定。本方法在5~1000μg/L浓度范围内,不同茶叶基质中草甘膦、氨甲基膦酸、草铵膦线性关系良好(R2>0.99)。在0.1,0.4和4 mg/kg添加水平下,不同茶叶(绿茶、红茶、乌龙茶、普洱茶)中3种化合物回收率均介于72.1%~109.9%之间,相对标准偏差RSD在0.5%~9.8%之间(n=6),方法定量限(LOQ)在0.03~0.08 mg/kg之间(S/N=10)。本方法稳定,简便,灵敏,能够满足检测需求。
建立瞭超高效液相色譜-串聯質譜同時快速測定不同茶葉中草甘膦、氨甲基膦痠及草銨膦的方法。樣品用0.05 mol/L NaOH提取,併以HCl調節pH值, Oasis HLB小柱淨化除雜,氯甲痠-9-芴基甲酯( FMOC-Cl)柱前衍生反應後,超高效液相色譜-串聯質譜法測定。本方法在5~1000μg/L濃度範圍內,不同茶葉基質中草甘膦、氨甲基膦痠、草銨膦線性關繫良好(R2>0.99)。在0.1,0.4和4 mg/kg添加水平下,不同茶葉(綠茶、紅茶、烏龍茶、普洱茶)中3種化閤物迴收率均介于72.1%~109.9%之間,相對標準偏差RSD在0.5%~9.8%之間(n=6),方法定量限(LOQ)在0.03~0.08 mg/kg之間(S/N=10)。本方法穩定,簡便,靈敏,能夠滿足檢測需求。
건립료초고효액상색보-천련질보동시쾌속측정불동다협중초감련、안갑기련산급초안련적방법。양품용0.05 mol/L NaOH제취,병이HCl조절pH치, Oasis HLB소주정화제잡,록갑산-9-물기갑지( FMOC-Cl)주전연생반응후,초고효액상색보-천련질보법측정。본방법재5~1000μg/L농도범위내,불동다협기질중초감련、안갑기련산、초안련선성관계량호(R2>0.99)。재0.1,0.4화4 mg/kg첨가수평하,불동다협(록다、홍다、오룡다、보이다)중3충화합물회수솔균개우72.1%~109.9%지간,상대표준편차RSD재0.5%~9.8%지간(n=6),방법정량한(LOQ)재0.03~0.08 mg/kg지간(S/N=10)。본방법은정,간편,령민,능구만족검측수구。
An efficient technique for the determination of multiclass pesticide residues ( glyphosate, aminomethyl phosphonic acid ( AMPA) and glufosinate) in four kinds of tea ( green tea, black tea, Oolong tea and Puer tea) was developed based on ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). Samples were extracted with 0. 05 mol/L NaOH solution, regulated pH value with HCl, followed by purification by Oasis HLB column, and then precolumn-derived with 9-fluorenylmethyl chloroformate ( FMOC-CL ) in borate buffer. All pesticide residues studied showed good linearity with correlation coefficient ( R2 ) greater than 0. 99 in the concentration range of 5-1000 μg/L. Limits of quantitation (LOQs) of three pesticide compounds ranged from 0. 03 to 0. 08 mg/kg (S/N=10). Tea samples spiked with 0 . 1 , 0 . 4 and 4 mg/kg showed the recovery ranging from 72 . 1% to 109 . 9%, and RSDs from 0. 5% to 9. 8% (n=6). In addition, the validated method was applied to commercial samples, and all the detections were confirmed by acquiring transitions for each pesticide in samples.