日用化学工业
日用化學工業
일용화학공업
CHINA SURFACTANT DETERGENT & CONSMETICS
2010年
2期
153-156
,共4页
武中平%卢剑%高巍%俞幼芬
武中平%盧劍%高巍%俞幼芬
무중평%로검%고외%유유분
化妆品%激素%测定%液相色谱-串联质谱法
化妝品%激素%測定%液相色譜-串聯質譜法
화장품%격소%측정%액상색보-천련질보법
cosmetics%hormones%determination%liquid chromatography together with mass spectrometry
采用液相色谱-串联质谱法测定化妆品中糖皮质激素、雌激素、雄激素、孕激素等激素的含量.不同形态的化妆品样品以甲醇为提取剂进行超声提取,样品提取液离心后得到上清液经HLB固相萃取小柱净化,用Agilent ZORBAX Eclipse XDB-C18柱(1.8 μm,2.1 mm ×50 mm),乙腈-水作为流动相,梯度洗脱,流速0.3 mL/min,柱温25 ℃,进样量2.0 μL,糖皮质激素、雄激素、孕激素采用正离子扫描模式,雌激素采用负离子扫描模式,多反应监测测定.化妆品样品平均加标回收率为72.31%~97.89%,相对标准偏差为2.24%~11.34%,方法检出限为0.002 mg/kg~0.8 mg/kg.
採用液相色譜-串聯質譜法測定化妝品中糖皮質激素、雌激素、雄激素、孕激素等激素的含量.不同形態的化妝品樣品以甲醇為提取劑進行超聲提取,樣品提取液離心後得到上清液經HLB固相萃取小柱淨化,用Agilent ZORBAX Eclipse XDB-C18柱(1.8 μm,2.1 mm ×50 mm),乙腈-水作為流動相,梯度洗脫,流速0.3 mL/min,柱溫25 ℃,進樣量2.0 μL,糖皮質激素、雄激素、孕激素採用正離子掃描模式,雌激素採用負離子掃描模式,多反應鑑測測定.化妝品樣品平均加標迴收率為72.31%~97.89%,相對標準偏差為2.24%~11.34%,方法檢齣限為0.002 mg/kg~0.8 mg/kg.
채용액상색보-천련질보법측정화장품중당피질격소、자격소、웅격소、잉격소등격소적함량.불동형태적화장품양품이갑순위제취제진행초성제취,양품제취액리심후득도상청액경HLB고상췌취소주정화,용Agilent ZORBAX Eclipse XDB-C18주(1.8 μm,2.1 mm ×50 mm),을정-수작위류동상,제도세탈,류속0.3 mL/min,주온25 ℃,진양량2.0 μL,당피질격소、웅격소、잉격소채용정리자소묘모식,자격소채용부리자소묘모식,다반응감측측정.화장품양품평균가표회수솔위72.31%~97.89%,상대표준편차위2.24%~11.34%,방법검출한위0.002 mg/kg~0.8 mg/kg.
Content of various kinds of hormones,including glucocorticoids,oestrogens,androgens and progestogen in cosmetics were determined by liquid chromatography together with mass spectrometry.Various cosmetics samples were extracted by methyl alcohol under help of ultrasonic wave.The extracts were centrifuged, and the upper clear solutions were purified by HLB SPE columns and separated with Agilent ZORBAX Eclipse XDB-C18 column (1.8 μm,2.1 mm ×50 mm),using a mobile phase consist of acetonitrile-water and gradient eluted at a flow rate of 0.3 mL/min.The column temperature was 25 ℃ and the injection volume was 2.0 μL.Glucocorticoids,androgens and progestogen were analyzed in the positive ion scanning mode,while oestrogens were analyzed in the negative ion scanning mode.The detections were made with MRM mode.The average recoveries achieve between 72.31% and 97.89%,and the relative standard deviations(RSD) achieve between 2.24% and 11.34%.The detection limits of this method achieves 0.002 mg/kg~0.8 mg/kg.