食品安全质量检测学报
食品安全質量檢測學報
식품안전질량검측학보
FOOD SAFETY AND QUALITY DETECTION TECHNOLOGY
2014年
12期
3769-3777
,共9页
王培锋%王凤美%张鸿伟%徐彪%邱芳%何京澄%周维政
王培鋒%王鳳美%張鴻偉%徐彪%邱芳%何京澄%週維政
왕배봉%왕봉미%장홍위%서표%구방%하경징%주유정
抗生素%动物源食品%Q-Exative高分辨质谱
抗生素%動物源食品%Q-Exative高分辨質譜
항생소%동물원식품%Q-Exative고분변질보
antibiotics%food of animal origin%Q-exactive high resolution mass spectrometry
目的:建立动物源食品中抗生素快速筛查的 Q-Exactive 方法。方法采用酸性乙腈提取动物源食品中的抗生素类化合物, QuEChERS净化,乙腈水定容, ACQUITY BEH C18色谱柱分离,以0.1%甲酸-乙腈为流动相,梯度洗脱分离。Q-Exactive 一级全扫描得到的准分子离子的精确质量数用于快速筛选分析,保留时间和离子阱的二级质谱数据用于进一步定性确证。结果31种抗生素的精确质量相对偏差小于5×10―6,线性相关系数均大于0.99,最低检出限(limit of detection, LOD)均≤10μg/kg。结论应用该方法对鱼、牛奶、蜂蜜等实际样品筛查的分析结果良好,说明该方法是动物源食品中抗生素类成分快速筛选和确证的有效方法。
目的:建立動物源食品中抗生素快速篩查的 Q-Exactive 方法。方法採用痠性乙腈提取動物源食品中的抗生素類化閤物, QuEChERS淨化,乙腈水定容, ACQUITY BEH C18色譜柱分離,以0.1%甲痠-乙腈為流動相,梯度洗脫分離。Q-Exactive 一級全掃描得到的準分子離子的精確質量數用于快速篩選分析,保留時間和離子阱的二級質譜數據用于進一步定性確證。結果31種抗生素的精確質量相對偏差小于5×10―6,線性相關繫數均大于0.99,最低檢齣限(limit of detection, LOD)均≤10μg/kg。結論應用該方法對魚、牛奶、蜂蜜等實際樣品篩查的分析結果良好,說明該方法是動物源食品中抗生素類成分快速篩選和確證的有效方法。
목적:건립동물원식품중항생소쾌속사사적 Q-Exactive 방법。방법채용산성을정제취동물원식품중적항생소류화합물, QuEChERS정화,을정수정용, ACQUITY BEH C18색보주분리,이0.1%갑산-을정위류동상,제도세탈분리。Q-Exactive 일급전소묘득도적준분자리자적정학질량수용우쾌속사선분석,보류시간화리자정적이급질보수거용우진일보정성학증。결과31충항생소적정학질량상대편차소우5×10―6,선성상관계수균대우0.99,최저검출한(limit of detection, LOD)균≤10μg/kg。결론응용해방법대어、우내、봉밀등실제양품사사적분석결과량호,설명해방법시동물원식품중항생소류성분쾌속사선화학증적유효방법。
Objective Todevelop a method of high performance liquid chromatography (HPLC) coupled with linear ion trap/Orbitrap high resolution mass spectrometry (QuEChERS) to detect antibiotics quickly in food of animal origin.Methods Antibiotics in samples were extracted using a solvent of acidic acetonitrile, following by purification with QuEChERS, dilution with acetonitrile and H2O. The separation was performed on an ACQUITY BEH C18column using gradient elution with aqueous solution (containing 0.1% formic acid)/acetonitrile as a mobile phase. The accurate mass of quasi-molecular ion were acquired by full scanning of electrostatic field orbitrap and applied for rapid screening and analysis, further confirmation was accomplished according to the retention time and qualitative fragments obtained by data dependent scan mode. ResultsUnder the optimal conditions, 31 antibiotics were routinely detected with mass accuracy error below 5×10―6, and good linearity were provided in their respective linear ranges with correlation coefficients all higher than 0.99, the limit of detection (LOD) for all the 31 antibiotics were≤10μg/kg. ConclusionThe method was applied to fish, milk, and honey and satisfying screening results proved that it is an efficient path for rapid analysis of antibiotics in food of animal origin.