茶叶科学
茶葉科學
다협과학
2014年
3期
271-278
,共8页
刘妍慧%于常红%刘岩%刘健%张婷
劉妍慧%于常紅%劉巖%劉健%張婷
류연혜%우상홍%류암%류건%장정
茶叶%基质固相分散萃取%高效液相色谱串联质谱%农药残留
茶葉%基質固相分散萃取%高效液相色譜串聯質譜%農藥殘留
다협%기질고상분산췌취%고효액상색보천련질보%농약잔류
tea%matrix solid-phase disperse extraction%HPLC-MS-MS%pesticide residues
建立了茶叶中3类11种农药的分散固相萃取-高效液相色谱串联质谱(HPLC-MS-MS)的检测方法。茶叶样品以乙腈-乙酸(体积比99∶1)提取,以PSA为净化剂基质固相分散萃取,然后通过C18色谱柱,以甲醇/水(含甲酸铵)溶液进行梯度洗脱,采用电离喷雾电离方式(ESI+),通过多反应监测(MRM)定量。结果表明:11种农药的分析时间约为20 min,在0~500 ng·mL-1范围内线性相关,相关系数大于0.9995,方法检测限为0.1~1.7μg·kg-1。测定了茶叶样品中11种农药的残留量,加标回收率为62.4%~114.8%(添加水平分别为10~400μg·kg-1),相对标准偏差(RSD)为3.28%~19.34%。选取了5个不同类型的茶叶样品,检测其中11种农药的残留量,检出结果差异较大。其中绿茶中11种农药的检出量为1.7~339.4μg·kg-1,加标回收率为86.1%~104.1%,相对标准偏差(RSD)均小于20%(n=6)。本方法准确、灵敏、简单、快速、安全,能满足茶叶样品中多种农药残留分析的要求。
建立瞭茶葉中3類11種農藥的分散固相萃取-高效液相色譜串聯質譜(HPLC-MS-MS)的檢測方法。茶葉樣品以乙腈-乙痠(體積比99∶1)提取,以PSA為淨化劑基質固相分散萃取,然後通過C18色譜柱,以甲醇/水(含甲痠銨)溶液進行梯度洗脫,採用電離噴霧電離方式(ESI+),通過多反應鑑測(MRM)定量。結果錶明:11種農藥的分析時間約為20 min,在0~500 ng·mL-1範圍內線性相關,相關繫數大于0.9995,方法檢測限為0.1~1.7μg·kg-1。測定瞭茶葉樣品中11種農藥的殘留量,加標迴收率為62.4%~114.8%(添加水平分彆為10~400μg·kg-1),相對標準偏差(RSD)為3.28%~19.34%。選取瞭5箇不同類型的茶葉樣品,檢測其中11種農藥的殘留量,檢齣結果差異較大。其中綠茶中11種農藥的檢齣量為1.7~339.4μg·kg-1,加標迴收率為86.1%~104.1%,相對標準偏差(RSD)均小于20%(n=6)。本方法準確、靈敏、簡單、快速、安全,能滿足茶葉樣品中多種農藥殘留分析的要求。
건립료다협중3류11충농약적분산고상췌취-고효액상색보천련질보(HPLC-MS-MS)적검측방법。다협양품이을정-을산(체적비99∶1)제취,이PSA위정화제기질고상분산췌취,연후통과C18색보주,이갑순/수(함갑산안)용액진행제도세탈,채용전리분무전리방식(ESI+),통과다반응감측(MRM)정량。결과표명:11충농약적분석시간약위20 min,재0~500 ng·mL-1범위내선성상관,상관계수대우0.9995,방법검측한위0.1~1.7μg·kg-1。측정료다협양품중11충농약적잔류량,가표회수솔위62.4%~114.8%(첨가수평분별위10~400μg·kg-1),상대표준편차(RSD)위3.28%~19.34%。선취료5개불동류형적다협양품,검측기중11충농약적잔류량,검출결과차이교대。기중록다중11충농약적검출량위1.7~339.4μg·kg-1,가표회수솔위86.1%~104.1%,상대표준편차(RSD)균소우20%(n=6)。본방법준학、령민、간단、쾌속、안전,능만족다협양품중다충농약잔류분석적요구。
A method for rapid determination of 11 kinds of pesticide residues in tea samples by matrix solid-phase disperse extraction and high performance liquid chromatography and tandem mass spectrometry was proposed. The pesticide residues in tea sample were firstly extracted by a mixture of V(acetonitrile)∶V(acetic acid)=99∶1, and the extract was solid-phase disperse purified by PSA and then separated on a Waters Xterra MS C18 column with a gradient system of a mixture of methanol and water with ammonium formate. Multi-reaction monitoring (MRM) was employed for quantitative determination. Eleven pesticide residues could be detected within 20 min. The linear range of 11 pesticide residue was 0-500 ng·mL-1 and the limits of detection were between 0.1-1.7μg·kg-1. The correlation rate was more than 0.9995. The average recoveries (spiked at the levels of 10-400μg·kg-1) ranged from 62.4% to 114.8% with relative standard deviation between 3.28% and 19.34%. After extraction and purification, 11 pesticide residues in 5 samples of different kinds of tea with significant variation in content were analyzed. And the residue content of 11 pesticides in green tea sample was 1.7-339.4μg·kg-1. Recoveries in this sample were ranged from 86.1%to 104.1%with relative standard deviations less than 20%. This method is accurate, sensitive, simple, rapid, safe and suitable for identification and quantification of multiple pesticide residues in tea.