食品研究与开发
食品研究與開髮
식품연구여개발
FOOD RESEARCH AND CEVELOPMENT
2013年
23期
37-40
,共4页
李彦%关丽丽%牟妍%孙磊丽%梁君妮%沙美兰%邹文晓%孙爱丽%曹鹏
李彥%關麗麗%牟妍%孫磊麗%樑君妮%沙美蘭%鄒文曉%孫愛麗%曹鵬
리언%관려려%모연%손뢰려%량군니%사미란%추문효%손애려%조붕
Quick,Easy,Cheap,Rugged,Safe(QuEChERS)%超高效液相色谱串联质谱%金刚烷胺%畜禽组织
Quick,Easy,Cheap,Rugged,Safe(QuEChERS)%超高效液相色譜串聯質譜%金剛烷胺%畜禽組織
Quick,Easy,Cheap,Rugged,Safe(QuEChERS)%초고효액상색보천련질보%금강완알%축금조직
Quick,Easy,Cheap,Rugged,Safe (QuEChERS)%ultra high performance liquid chromatography-tandem mass spectrometry%amantadine%livestock and poultry tissues
建立一种QuEChERS-超高效液相色谱-串联质谱(QuEChERS-UPLC-MS/MS)检测畜禽组织中金刚烷胺残留的方法。样品用1%乙酸乙腈溶液超声提取,提取液加入C18和PSA填料进行基质分散固相净化,浓缩后经Proshell 120 EC-C18柱分离,用电喷雾离子源正离子多反应监测(MRM)模式进行检测。在0.2μg/L~100.0μg/L线性范围内具有较好的线性关系,相关系数大于0.997。该方法检出限(LOD)为0.6μg/kg,定量限(LOQ)为2.0μg/kg,回收率为70.5%~100.1%,相对标准偏差(RSD)小于10%。该方法简便快速、准确度好,适用于畜禽组织中金刚烷胺药物残留的检测。
建立一種QuEChERS-超高效液相色譜-串聯質譜(QuEChERS-UPLC-MS/MS)檢測畜禽組織中金剛烷胺殘留的方法。樣品用1%乙痠乙腈溶液超聲提取,提取液加入C18和PSA填料進行基質分散固相淨化,濃縮後經Proshell 120 EC-C18柱分離,用電噴霧離子源正離子多反應鑑測(MRM)模式進行檢測。在0.2μg/L~100.0μg/L線性範圍內具有較好的線性關繫,相關繫數大于0.997。該方法檢齣限(LOD)為0.6μg/kg,定量限(LOQ)為2.0μg/kg,迴收率為70.5%~100.1%,相對標準偏差(RSD)小于10%。該方法簡便快速、準確度好,適用于畜禽組織中金剛烷胺藥物殘留的檢測。
건립일충QuEChERS-초고효액상색보-천련질보(QuEChERS-UPLC-MS/MS)검측축금조직중금강완알잔류적방법。양품용1%을산을정용액초성제취,제취액가입C18화PSA전료진행기질분산고상정화,농축후경Proshell 120 EC-C18주분리,용전분무리자원정리자다반응감측(MRM)모식진행검측。재0.2μg/L~100.0μg/L선성범위내구유교호적선성관계,상관계수대우0.997。해방법검출한(LOD)위0.6μg/kg,정량한(LOQ)위2.0μg/kg,회수솔위70.5%~100.1%,상대표준편차(RSD)소우10%。해방법간편쾌속、준학도호,괄용우축금조직중금강완알약물잔류적검측。
A method for the determination of the residues of amantadine in livestock and poultry tissues by QuEChERS extraction and ultra high performance liquid chromatograph-tandem mass spectrometric method (UPLC-MS/MS) was established. The sample was extracted with acetonitrile (containing 1%acetic acid) and followed by ultrasound. Cleanup of the extracts was processed by C18 and PSA , a modified dispersive solid phase extraction (QuEChERS). The analysts were then separated by Poroshell 120 EC-C18 column, and finally detected by tandem mass spectrometry in positive ESI mode. The linearity of amantadine in the range from 0.2 μg/kg to 100.0μg/kg had correlation coefficient greater than 0.997. The limits of detection (LOD) of the method were 0.6μg/kg and the limits of quantification (LOQ) were 2.0μg/kg. The average recoveries of amantadine were in the range from 70.5%to 100.1%, with relative standard deviations were less than 10%.The established method is sensitive and of good recoveries. It applies to the determination of the residues of amantadine in poultry tissues and meat.