食品科学
食品科學
식품과학
FOOD SCIENCE
2010年
2期
120-123
,共4页
孙玉增%徐英江%刘慧慧%张世娟%秦华伟%高继庆
孫玉增%徐英江%劉慧慧%張世娟%秦華偉%高繼慶
손옥증%서영강%류혜혜%장세연%진화위%고계경
液相色谱-串联质谱(UPLC-MS/MS)%水产品%磺胺类药物
液相色譜-串聯質譜(UPLC-MS/MS)%水產品%磺胺類藥物
액상색보-천련질보(UPLC-MS/MS)%수산품%광알류약물
UPLC-MS/MS%aquatic products%sulfonamide residues
研究一种能够同时测定水产品中21种磺胺类药物残留量的检测方法--超高效液相色谱质谱法.样品经乙酸乙酯提取,经固相萃取小柱净化,氮气吹干后,用1mL流动相定容残余物.采用ACQUITY~(TM) BEH C_(18)色谱柱,用甲醇和5mmol/L乙酸铵溶液(含体积分数0.1%甲酸)作流动相,采用质谱技术分析.结果表明,检出限为0.01~0.20μg/kg,定量限为0.03~0.67μg/kg,平均回收率为68%~82%,相对标准偏差为4.1%~11.8%.该方法适合水产品中多种磺胺类药物的检测.
研究一種能夠同時測定水產品中21種磺胺類藥物殘留量的檢測方法--超高效液相色譜質譜法.樣品經乙痠乙酯提取,經固相萃取小柱淨化,氮氣吹榦後,用1mL流動相定容殘餘物.採用ACQUITY~(TM) BEH C_(18)色譜柱,用甲醇和5mmol/L乙痠銨溶液(含體積分數0.1%甲痠)作流動相,採用質譜技術分析.結果錶明,檢齣限為0.01~0.20μg/kg,定量限為0.03~0.67μg/kg,平均迴收率為68%~82%,相對標準偏差為4.1%~11.8%.該方法適閤水產品中多種磺胺類藥物的檢測.
연구일충능구동시측정수산품중21충광알류약물잔류량적검측방법--초고효액상색보질보법.양품경을산을지제취,경고상췌취소주정화,담기취간후,용1mL류동상정용잔여물.채용ACQUITY~(TM) BEH C_(18)색보주,용갑순화5mmol/L을산안용액(함체적분수0.1%갑산)작류동상,채용질보기술분석.결과표명,검출한위0.01~0.20μg/kg,정량한위0.03~0.67μg/kg,평균회수솔위68%~82%,상대표준편차위4.1%~11.8%.해방법괄합수산품중다충광알류약물적검측.
An ultra performance liquid chromatography-electrospray ionization tandem mass spectrometric (UPLC-MS/MS) method has been developed for the simultaneous determination of 21 sulfonamide residues in aquatic products.Samples were extracted with ethyl acetate,cleaned up using an HLB SPE cartridge and blown to dryness under nitrogen,and the residues were then dissolved in 1 mL of mobile phase.The 21 analytes were separated on ACQUITY~(TM) BEH C_(18) column with a mobile phase composed of methanol and 5 mmol/L aqueous ammonium acetate solution (containing 0.1% formic acid).The limits for qualitative detection and quantitative determination were 0.01- 0.20μg/kg and 0.03-0.67μg/kg,respectively.The average recoveries at three spike levels ranged 68%-82%,with RSDs ranging 4.1%-11.8%.All these figures of merit demonstrate a good suitability of this method for the simultaneous determination of sulfonamide residues in aquatic products.