色谱
色譜
색보
CHINESE JOURNAL OF CHROMATOGRAPHY
2009年
6期
856-859
,共4页
马强%王超%白桦%王星%张庆%肖海清%闫研%董益阳%王宝麟
馬彊%王超%白樺%王星%張慶%肖海清%閆研%董益暘%王寶麟
마강%왕초%백화%왕성%장경%초해청%염연%동익양%왕보린
同位素稀释%液相色谱-串联质谱%丙烯酰胺%化妆品
同位素稀釋%液相色譜-串聯質譜%丙烯酰胺%化妝品
동위소희석%액상색보-천련질보%병희선알%화장품
isotope dilution%liquid chromatography-tandem mass spectrometry (LC-MS/MS)%acrylamide%cosmetics
建立了化妆品中丙烯酰胺残留的同位素稀释液相色谱-串联质谱的分析方法.水溶性化妆品样品以水为提取溶剂进行提取,提取液经高速离心处理后,上清液用Oasis HLB固相萃取柱净化;脂溶性化妆品样品以正己烷和水混合溶剂液-液分配萃取.经Waters Atlantis T3色谱柱(150 mm×2.1 mm,3 μm)分离后在多反应监测模式下进行串联质谱定性及定量分析,以~(13)C_3-丙烯酰胺为内标定量.方法的定量限为0.1 mg/kg,在0.1~1.0 mg/kg 3个添加水平范围内的平均回收率为87.7% ~95.8%,日内测定精密度均小于10%,日间测定精密度均小于12% .该方法能够满足化妆品中丙烯酰胺残留的检测要求.
建立瞭化妝品中丙烯酰胺殘留的同位素稀釋液相色譜-串聯質譜的分析方法.水溶性化妝品樣品以水為提取溶劑進行提取,提取液經高速離心處理後,上清液用Oasis HLB固相萃取柱淨化;脂溶性化妝品樣品以正己烷和水混閤溶劑液-液分配萃取.經Waters Atlantis T3色譜柱(150 mm×2.1 mm,3 μm)分離後在多反應鑑測模式下進行串聯質譜定性及定量分析,以~(13)C_3-丙烯酰胺為內標定量.方法的定量限為0.1 mg/kg,在0.1~1.0 mg/kg 3箇添加水平範圍內的平均迴收率為87.7% ~95.8%,日內測定精密度均小于10%,日間測定精密度均小于12% .該方法能夠滿足化妝品中丙烯酰胺殘留的檢測要求.
건립료화장품중병희선알잔류적동위소희석액상색보-천련질보적분석방법.수용성화장품양품이수위제취용제진행제취,제취액경고속리심처리후,상청액용Oasis HLB고상췌취주정화;지용성화장품양품이정기완화수혼합용제액-액분배췌취.경Waters Atlantis T3색보주(150 mm×2.1 mm,3 μm)분리후재다반응감측모식하진행천련질보정성급정량분석,이~(13)C_3-병희선알위내표정량.방법적정량한위0.1 mg/kg,재0.1~1.0 mg/kg 3개첨가수평범위내적평균회수솔위87.7% ~95.8%,일내측정정밀도균소우10%,일간측정정밀도균소우12% .해방법능구만족화장품중병희선알잔류적검측요구.
A comprehensive analytical method based on isotope dilution-liquid chromatography-tandem mass spectrometry (LC-MS/MS) has been developed for the determination of acrylam-ide residue in cosmetics. Water-soluble cosmetic sample was extracted with water, and the ex-tract was centrifuged, then the upper solution was cleaned up by an Oasis HLB solid phase ex-traction cartridge. Oil-soluble cosmetic sample was extracted by liquid-liquid partition with n-hexane and water. The qualitative and quantitative analyses were carried out for the analyte in the multiple reaction monitoring (MRM) mode after the chromatographic separation on a Wa-ters Atlantis T3 column (150 mm × 2. 1 mm, 3 μm). The quantification was performed with ~(13)C_3-acrylamide as internal standard. The limit of quantification (LOQ) for acrylamide was 0. 1 mg/kg. The mean recoveries were 87. 7% -95. 8% at the spiked levels of 0.1-1.0 mg/kg with the intra-day precision less than 10% and the inter-day precision less than 12%. The method is suitable for the determination of acrylamide in cosmetics.