色谱
色譜
색보
CHINESE JOURNAL OF CHROMATOGRAPHY
2010年
3期
301-304
,共4页
李立%付建%高洪良%任海涛%娄喜山%管立辉
李立%付建%高洪良%任海濤%婁喜山%管立輝
리립%부건%고홍량%임해도%루희산%관립휘
高效液相色谱-串联质谱法%固相萃取%杀草强%农产品
高效液相色譜-串聯質譜法%固相萃取%殺草彊%農產品
고효액상색보-천련질보법%고상췌취%살초강%농산품
high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS)%solid-phase extraction (SPE)%amitrole%agricultural products
建立了采用高效液相色谱-串联质谱法(HPLC-MS/MS)检测多种农产品中杀草强残留量的方法.根据样品基质不同,分别采用25%丙酮水溶液(针对小麦、鱼、肉和肝脏样品)、1%乙酸酸化的25%丙酮水溶液(针对玉米和花生样品)、1%乙酸水溶液(针对金银花、姜粉、花椒粉和茶叶样品)及1%乙酸水溶液和二氯甲烷(针对苹果、菠萝、菠菜、胡萝卜和紫苏叶)进行提取,然后依次采用二氯甲烷萃取、PCX或ENVI-Carb固相萃取柱净化后,进行HPLC-MS/MS测定,外标法定量.在0.005~0.1 mg/kg范围内,杀草强的峰面积与其质量浓度有良好的线性关系,相关系数为 0.999 7.对上述15种不同种类的农产品进行添加回收,回收率为67.5% ~98.1% ,相对标准偏差为1.0% ~9.8% .苹果、菠菜、紫苏叶、玉米、姜、鱼和肉等样品的定量限为0.01 mg/kg,茶叶、金银花、花椒粉的定量限为0.02 mg/kg.该方法的灵敏度、准确度和精密度均符合农药残留测定的技术要求.
建立瞭採用高效液相色譜-串聯質譜法(HPLC-MS/MS)檢測多種農產品中殺草彊殘留量的方法.根據樣品基質不同,分彆採用25%丙酮水溶液(針對小麥、魚、肉和肝髒樣品)、1%乙痠痠化的25%丙酮水溶液(針對玉米和花生樣品)、1%乙痠水溶液(針對金銀花、薑粉、花椒粉和茶葉樣品)及1%乙痠水溶液和二氯甲烷(針對蘋果、菠蘿、菠菜、鬍蘿蔔和紫囌葉)進行提取,然後依次採用二氯甲烷萃取、PCX或ENVI-Carb固相萃取柱淨化後,進行HPLC-MS/MS測定,外標法定量.在0.005~0.1 mg/kg範圍內,殺草彊的峰麵積與其質量濃度有良好的線性關繫,相關繫數為 0.999 7.對上述15種不同種類的農產品進行添加迴收,迴收率為67.5% ~98.1% ,相對標準偏差為1.0% ~9.8% .蘋果、菠菜、紫囌葉、玉米、薑、魚和肉等樣品的定量限為0.01 mg/kg,茶葉、金銀花、花椒粉的定量限為0.02 mg/kg.該方法的靈敏度、準確度和精密度均符閤農藥殘留測定的技術要求.
건립료채용고효액상색보-천련질보법(HPLC-MS/MS)검측다충농산품중살초강잔류량적방법.근거양품기질불동,분별채용25%병동수용액(침대소맥、어、육화간장양품)、1%을산산화적25%병동수용액(침대옥미화화생양품)、1%을산수용액(침대금은화、강분、화초분화다협양품)급1%을산수용액화이록갑완(침대평과、파라、파채、호라복화자소협)진행제취,연후의차채용이록갑완췌취、PCX혹ENVI-Carb고상췌취주정화후,진행HPLC-MS/MS측정,외표법정량.재0.005~0.1 mg/kg범위내,살초강적봉면적여기질량농도유량호적선성관계,상관계수위 0.999 7.대상술15충불동충류적농산품진행첨가회수,회수솔위67.5% ~98.1% ,상대표준편차위1.0% ~9.8% .평과、파채、자소협、옥미、강、어화육등양품적정량한위0.01 mg/kg,다협、금은화、화초분적정량한위0.02 mg/kg.해방법적령민도、준학도화정밀도균부합농약잔류측정적기술요구.
A high performance liquid chromatography-tandem mass spectrometry method (HPLC-MS/MS) was developed for the analysis of amitrole residues in agricultural products.The samples were extracted by 25% acetone for wheat,fish,pork and liver samples,1% acetic acid-25% acetone for maize and peanut samples,1% acetic acid solution for honeysuckle,the powder of ginger,the powder of bunge prickly ash and tea leaves samples,1% acetic acid solution-dichloromethane for apple,pineapple,spinach,carrot,perilla leaves samples,respectively,followed by liquid-liquid extraction with dichloromethane.The samples were then cleaned up by PCX or Envi-Carb solid-phase extraction cartridge.The amitrole was determined and confirmed by HPLC-MS/MS.The results showed a linear relationship in the range of 0.005-0.1 mg/kg for amitrole.The correlation coefficient was 0.999 7.The average recoveries of amitrole in wheat,maize,peanut,pineapple,apple,carrot,spinach,pork,the powder of ginger,the powder of bunge prickly ash,perilla,liver,fish,honeysuckle and tea were 67.5% -98.1% .The relative standard deviations (RSDs) were 1.0% -9.8% .The limits of quantitation were 10μg/kg for wheat,maize,peanut,pineapple,apple,carrot,spinach,pork,perilla,liver,fish,honeysuckle and 20μg/kg for the powder of bunge prickly ash,the powder of ginger and tea,respectively.The method is simple,sensitive and accurate.