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
8期
2462-2469
,共8页
静平%张金斗%朱文彬%鲍蕾%于冰%吴振兴%梁成珠
靜平%張金鬥%硃文彬%鮑蕾%于冰%吳振興%樑成珠
정평%장금두%주문빈%포뢰%우빙%오진흥%량성주
邻苯二甲酸酯%双酚A%高效液相色谱-串联质谱
鄰苯二甲痠酯%雙酚A%高效液相色譜-串聯質譜
린분이갑산지%쌍분A%고효액상색보-천련질보
phthalate esters%bisphenol A%high performance liquid chromatography-tandem mass spectrometry
目的:建立了饮料、牛奶和奶粉中双酚A及15种邻苯二甲酸酯的高效液相色谱-串联质谱分析方法。方法样品经甲醇提取, C18色谱柱分离后,采用串联四极杆质谱电喷雾电离源正负离子切换多反应离子监测模式检测。结果双酚A及15种邻苯二甲酸酯在各自的线性范围内线性关系良好,相关系数均不低于0.9900,定量下限为10μg/kg,低、中、高3个加标水平下平均回收率为61.1%~129.5%,相对标准偏差为1.13%~22.12%。结论该方法具有前处理简单、灵敏度高的优点,适用于饮料、牛奶及奶粉中双酚A及15种邻苯二甲酸酯残留的确证和定量检测。
目的:建立瞭飲料、牛奶和奶粉中雙酚A及15種鄰苯二甲痠酯的高效液相色譜-串聯質譜分析方法。方法樣品經甲醇提取, C18色譜柱分離後,採用串聯四極桿質譜電噴霧電離源正負離子切換多反應離子鑑測模式檢測。結果雙酚A及15種鄰苯二甲痠酯在各自的線性範圍內線性關繫良好,相關繫數均不低于0.9900,定量下限為10μg/kg,低、中、高3箇加標水平下平均迴收率為61.1%~129.5%,相對標準偏差為1.13%~22.12%。結論該方法具有前處理簡單、靈敏度高的優點,適用于飲料、牛奶及奶粉中雙酚A及15種鄰苯二甲痠酯殘留的確證和定量檢測。
목적:건립료음료、우내화내분중쌍분A급15충린분이갑산지적고효액상색보-천련질보분석방법。방법양품경갑순제취, C18색보주분리후,채용천련사겁간질보전분무전리원정부리자절환다반응리자감측모식검측。결과쌍분A급15충린분이갑산지재각자적선성범위내선성관계량호,상관계수균불저우0.9900,정량하한위10μg/kg,저、중、고3개가표수평하평균회수솔위61.1%~129.5%,상대표준편차위1.13%~22.12%。결론해방법구유전처리간단、령민도고적우점,괄용우음료、우내급내분중쌍분A급15충린분이갑산지잔류적학증화정량검측。
Objective A method for the simultaneous determination of bisphenol A (BPA) and fifteen phthalate esters (PAEs) by high performance liquid chromatography-tandem mass spectrometry was established. Methods The samples were extracted by methanol. The target compounds were separated by C18 column and detected by MS/MS system with eletrospray ionization (ESI) positive and negative ion mode under multiple reaction monitoring (MRM) mode. Results High correlation coefficients (r≥0.9900) of sixteen compounds were obtained within their respective linear ranges. The LOQ of BPA and 15 PAEs was 10 μg/kg. The recoveries ranged from 61.1%~129.5%, with the relative standard deviations of 1.13%~22.12%. Conclusion This method is suitable for the identification and quantification of PAEs and BPA in beverage, milk and milk powder with advantages of simple pretreatment, good purification and high sensitivity.