华南农业大学学报
華南農業大學學報
화남농업대학학보
JOURNAL OF SOUTH CHINA AGRICULTURAL UNIVERSITY
2014年
4期
16-21
,共6页
李帅鹏%黄显会%许颖%郭春娜%孔祥凯
李帥鵬%黃顯會%許穎%郭春娜%孔祥凱
리수붕%황현회%허영%곽춘나%공상개
高效液相色谱-串联质谱%阿莫西林%奶%残留检测
高效液相色譜-串聯質譜%阿莫西林%奶%殘留檢測
고효액상색보-천련질보%아막서림%내%잔류검측
high performance liquid chromatography-tandem mass spectrometry ( HPLC-MS/MS )%amoxicillin%milk%residue determination
【目的】建立奶中阿莫西林残留检测的高效液相色谱-串联质谱方法.【方法】2g样品经乙醇沉淀蛋白质后,转入梨形瓶中旋转蒸发浓缩至约0.5 mL左右,用pH 4.5乙酸铵溶液定容,净化后检测.流动相为乙腈和体积分数0.1%甲酸水溶液,梯度洗脱,经Luna 5μm C18色谱柱分离,采用电喷雾电离,多反应监测正离子模式对阿莫西林进行定量分析.【结果和结论】采用基质匹配法对奶中阿莫西林的含量进行标准校正,在阿莫西林质量浓度为1~400μg· L-1范围内呈现良好的线性关系,相关系数>0.999;奶中加标样品的检出限(按信噪比 S/N≥3计)为1μg· kg-1,定量限(按信噪比S/N≥10计)为2μg· kg-1.在定量限、1/2最高残留限量(5μg· kg -1)、最高残留限量(10μg· kg-1)、2倍最高残留限量(20μg· kg-1)添加水平下,奶中阿莫西林的平均回收率为75.6%~91.0%,相对标准偏差为1.6%~10.2%.
【目的】建立奶中阿莫西林殘留檢測的高效液相色譜-串聯質譜方法.【方法】2g樣品經乙醇沉澱蛋白質後,轉入梨形瓶中鏇轉蒸髮濃縮至約0.5 mL左右,用pH 4.5乙痠銨溶液定容,淨化後檢測.流動相為乙腈和體積分數0.1%甲痠水溶液,梯度洗脫,經Luna 5μm C18色譜柱分離,採用電噴霧電離,多反應鑑測正離子模式對阿莫西林進行定量分析.【結果和結論】採用基質匹配法對奶中阿莫西林的含量進行標準校正,在阿莫西林質量濃度為1~400μg· L-1範圍內呈現良好的線性關繫,相關繫數>0.999;奶中加標樣品的檢齣限(按信譟比 S/N≥3計)為1μg· kg-1,定量限(按信譟比S/N≥10計)為2μg· kg-1.在定量限、1/2最高殘留限量(5μg· kg -1)、最高殘留限量(10μg· kg-1)、2倍最高殘留限量(20μg· kg-1)添加水平下,奶中阿莫西林的平均迴收率為75.6%~91.0%,相對標準偏差為1.6%~10.2%.
【목적】건립내중아막서림잔류검측적고효액상색보-천련질보방법.【방법】2g양품경을순침정단백질후,전입리형병중선전증발농축지약0.5 mL좌우,용pH 4.5을산안용액정용,정화후검측.류동상위을정화체적분수0.1%갑산수용액,제도세탈,경Luna 5μm C18색보주분리,채용전분무전리,다반응감측정리자모식대아막서림진행정량분석.【결과화결론】채용기질필배법대내중아막서림적함량진행표준교정,재아막서림질량농도위1~400μg· L-1범위내정현량호적선성관계,상관계수>0.999;내중가표양품적검출한(안신조비 S/N≥3계)위1μg· kg-1,정량한(안신조비S/N≥10계)위2μg· kg-1.재정량한、1/2최고잔류한량(5μg· kg -1)、최고잔류한량(10μg· kg-1)、2배최고잔류한량(20μg· kg-1)첨가수평하,내중아막서림적평균회수솔위75.6%~91.0%,상대표준편차위1.6%~10.2%.
Objective] An analytical method was developed for the determination of amoxicillin residues in milk by high performance liquid chromatography-tandem mass spectrometry ( HPLC-MS/MS) .[Meth-od] A two-gram milk sample was deproteinized by ethanol .The supernatant was transferred into a pear-shaped bottle to be evaporated to about 0.5 mL,and the residue was dissolved with ammonium acetate so-lution.The sample was determined by HPLC-MS/MS after the purification.The chromatographic separa-tion was achieved on a Luna 5μm C18 column using 0.1%formic acid in water and acetonitrile as mobile phases with gradient elution .The identification of amoxicillin was carried out by MS/MS equipped with electrospray ionization in positive scanning and multiple reaction monitoring (MRM) modes.[Result and conclusion] Matrix-matched calibration standard was used for the quantification .The calibration curve showed perfect linearity in the range of 1-400μg· L-1 , with the correlation coefficient being more than 0.999.The limit of detection (LOD,S/N≥3) was 1 μg· kg-1 in milk,and the limit of quantification ( LOQ,S/N≥10) was 2μg· kg-1 .The mean recoveries varied from 75.6%to 91.0%at the four spiked levels of LOQ,1/2MRL (the maximum residue limit:5μg· kg-1 ), MRL(10 μg· kg -1 ),and 2MRL(20μg· kg-1 ) with the relative standard deviations of 1.6%-10.2%.