现代农药
現代農藥
현대농약
MODERN AGROCHEMICALS
2013年
4期
36-39
,共4页
占绣萍%马青%余淑红%马琳
佔繡萍%馬青%餘淑紅%馬琳
점수평%마청%여숙홍%마림
蔬菜%杀虫剂%液相色谱%残留
蔬菜%殺蟲劑%液相色譜%殘留
소채%살충제%액상색보%잔류
vegetable%insecticide%HPLC%residue
建立了大白菜、豇豆、花菜、番茄等蔬菜中氟啶虫酰胺、氯虫苯甲酰胺、甲氧虫酰肼、氟苯虫酰胺、虫螨腈和虱螨脲等6种杀虫剂残留的液相色谱检测方法。蔬菜经乙腈高速匀浆提取,过NH 2-SPE小柱净化,再用甲醇定容。以甲醇+乙腈+水为流动相,利用C 18柱和紫外检测器(检测波长:265,254,230 nm)对待测组分进行分离和测定。结果表明:添加浓度在0.1,0.5,1.0 mg/kg时,蔬菜中氟啶虫酰胺、氯虫苯甲酰胺、甲氧虫酰肼、氟苯虫酰胺、虫螨腈和虱螨脲的平均添加回收率在88.9%~119.2%之间,相对标准偏差(RSD)为0.26%~11.56%,仪器的最小检出量为1 ng,这6种农药在样品中的最低检测浓度为0.05 mg/kg。
建立瞭大白菜、豇豆、花菜、番茄等蔬菜中氟啶蟲酰胺、氯蟲苯甲酰胺、甲氧蟲酰肼、氟苯蟲酰胺、蟲螨腈和虱螨脲等6種殺蟲劑殘留的液相色譜檢測方法。蔬菜經乙腈高速勻漿提取,過NH 2-SPE小柱淨化,再用甲醇定容。以甲醇+乙腈+水為流動相,利用C 18柱和紫外檢測器(檢測波長:265,254,230 nm)對待測組分進行分離和測定。結果錶明:添加濃度在0.1,0.5,1.0 mg/kg時,蔬菜中氟啶蟲酰胺、氯蟲苯甲酰胺、甲氧蟲酰肼、氟苯蟲酰胺、蟲螨腈和虱螨脲的平均添加迴收率在88.9%~119.2%之間,相對標準偏差(RSD)為0.26%~11.56%,儀器的最小檢齣量為1 ng,這6種農藥在樣品中的最低檢測濃度為0.05 mg/kg。
건립료대백채、강두、화채、번가등소채중불정충선알、록충분갑선알、갑양충선정、불분충선알、충만정화슬만뇨등6충살충제잔류적액상색보검측방법。소채경을정고속균장제취,과NH 2-SPE소주정화,재용갑순정용。이갑순+을정+수위류동상,이용C 18주화자외검측기(검측파장:265,254,230 nm)대대측조분진행분리화측정。결과표명:첨가농도재0.1,0.5,1.0 mg/kg시,소채중불정충선알、록충분갑선알、갑양충선정、불분충선알、충만정화슬만뇨적평균첨가회수솔재88.9%~119.2%지간,상대표준편차(RSD)위0.26%~11.56%,의기적최소검출량위1 ng,저6충농약재양품중적최저검측농도위0.05 mg/kg。
A high-performance liquid chromatography (HPLC) method was developed for the determination of flonicamid, chlorantraniliprole, methoxyfenozide, flubendiamide, chlorfenapyr and lufenuron residues in vegetables such as Chinese cabbage, cowpea, cauliflower and tomato. The vegetable samples were extracted with acetonitrile, cleaned up with NH 2-SPE columns, and condensed to dry. Determinations of the analytes were completed by HPLC with DAD at 265, 254 and 230 nm. The results showed that the fortified recoveries of these six insecticides in vegetable samples were in the range of 88.9%-119.2%, with the relative standard deviations of 0.26%-11.56%. The limit of detection was 1 ng, and the limits of quantification of the six insecticides were 0.05 mg/kg in these vegetable samples.