色谱
色譜
색보
CHINESE JOURNAL OF CHROMATOGRAPHY
2015年
6期
590-596
,共7页
李欣%张瑶琴%艾连峰%王学生%王曼曼%徐厚君%郝玉兰
李訢%張瑤琴%艾連峰%王學生%王曼曼%徐厚君%郝玉蘭
리흔%장요금%애련봉%왕학생%왕만만%서후군%학옥란
疏水整体柱%在线固相萃取%高效液相色谱-串联质谱%阿维菌素类药物%牛肝
疏水整體柱%在線固相萃取%高效液相色譜-串聯質譜%阿維菌素類藥物%牛肝
소수정체주%재선고상췌취%고효액상색보-천련질보%아유균소류약물%우간
hydrophobic monolithic column%on-line solid-phase extraction%high performance liquid chromatography-tandem mass spectrometry(HPLC-MS/MS)%avermectins%bovine liver
建立了牛肝中5种阿维菌素类药物残留的疏水整体柱在线固相萃取结合高效液相色谱-串联质谱测定的方法。以疏水的聚(甲基丙烯酸丁酯-乙二醇二甲基丙烯酸酯)整体柱(10 mm×2.1 mm)作为固相萃取介质,考察了上样流动相和洗脱流速对阿维菌素类药物的萃取效果,优化了梯度洗脱流动相的种类及质谱条件。方法在1~100μg/L范围内线性关系良好( r﹥0.995),定量限为5μg/kg。在5、10、50、100μg/kg 添加水平的回收率为77.4%~98.4%,日内和日间相对标准偏差分别为4.46%~8.03%和4.79%~8.68%,并且该柱反复使用400次后未发现萃取效率降低。结果表明,该整体柱对牛肝中5种阿维菌素类药物能够有效萃取,并且可以重复使用。该方法简单,自动化程度高,可应用于常规阿维菌素类药物残留分析。
建立瞭牛肝中5種阿維菌素類藥物殘留的疏水整體柱在線固相萃取結閤高效液相色譜-串聯質譜測定的方法。以疏水的聚(甲基丙烯痠丁酯-乙二醇二甲基丙烯痠酯)整體柱(10 mm×2.1 mm)作為固相萃取介質,攷察瞭上樣流動相和洗脫流速對阿維菌素類藥物的萃取效果,優化瞭梯度洗脫流動相的種類及質譜條件。方法在1~100μg/L範圍內線性關繫良好( r﹥0.995),定量限為5μg/kg。在5、10、50、100μg/kg 添加水平的迴收率為77.4%~98.4%,日內和日間相對標準偏差分彆為4.46%~8.03%和4.79%~8.68%,併且該柱反複使用400次後未髮現萃取效率降低。結果錶明,該整體柱對牛肝中5種阿維菌素類藥物能夠有效萃取,併且可以重複使用。該方法簡單,自動化程度高,可應用于常規阿維菌素類藥物殘留分析。
건립료우간중5충아유균소류약물잔류적소수정체주재선고상췌취결합고효액상색보-천련질보측정적방법。이소수적취(갑기병희산정지-을이순이갑기병희산지)정체주(10 mm×2.1 mm)작위고상췌취개질,고찰료상양류동상화세탈류속대아유균소류약물적췌취효과,우화료제도세탈류동상적충류급질보조건。방법재1~100μg/L범위내선성관계량호( r﹥0.995),정량한위5μg/kg。재5、10、50、100μg/kg 첨가수평적회수솔위77.4%~98.4%,일내화일간상대표준편차분별위4.46%~8.03%화4.79%~8.68%,병차해주반복사용400차후미발현췌취효솔강저。결과표명,해정체주대우간중5충아유균소류약물능구유효췌취,병차가이중복사용。해방법간단,자동화정도고,가응용우상규아유균소류약물잔류분석。
A method based on on-line solid-phase extraction( SPE)with hydrophobic mono-lithic column coupled with high performance liquid chromatography-tandem mass spectrometry was developed for the simultaneous determination of five avermectins in bovine liver. A poly( butyl methacrylate-co-ethylene dimethacrylate)monolithic column was used as the sor-bent. The parameters influenced on on-line SPE and separation process such as the loading mobile phase,the eluting flow rate and the solvent for the separation were investigated in detail. Blank samples,spiked samples,matrix effect and recovery experiments were investiga-ted to evaluate the extraction efficiency and potential interfering compounds originating from the matrix. Under the optimized conditions,the method showed a linear range of 1-100 μg/L and the quantification limit of 5 μg/kg for each analyte. The presented method gave recoveries of 77. 4% -98. 4%. The relative standard deviations of intra-day and inter-day were 4. 46% -8. 03% and 4. 79%-8. 68%,respectively. Moreover,no significant changes were found in the extraction performance after more than 400 usages on one monolithic column,and even on the monoliths with various batches. The feasibility of the developed poly( butyl methacrylate-co-ethylene dimethacrylate)monolithic column based on the on-line SPE method for the determi-nation of avermectins was further demonstrated by the analysis of real samples.