分析化学
分析化學
분석화학
CHINESE JOURNAL OF ANALYTICAL CHEMISTRY
2014年
10期
1441-1446
,共6页
韩婉清%罗海英%陈立伟%吴玉銮%冼燕萍%王斌
韓婉清%囉海英%陳立偉%吳玉鑾%冼燕萍%王斌
한완청%라해영%진립위%오옥란%승연평%왕빈
磷酸三酯%稳定同位素内标%化妆品%气相色谱-质谱联用法
燐痠三酯%穩定同位素內標%化妝品%氣相色譜-質譜聯用法
린산삼지%은정동위소내표%화장품%기상색보-질보련용법
Organophosphate ester%Stable isotope-labeled internal standard%Cosmetic%Gas chromatography-mass spectrometry
根据不同化妆品的基质特性探讨优化不同的提取净化方法,建立了稳定同位素稀释气相色谱-质谱联用测定化妆品中5种磷酸三酯类化合物( OPEs)的方法。膏霜乳液类和蜡基类化妆品经溶剂提取后,采用ENVI-Carb固相萃取柱净化;粉剂类和水剂类化妆品经溶剂提取、浓缩后直接检测。样液经DB-5MS(30 m×0.25 mm×0.25μm)色谱柱分离,GC-MS的选择离子监测( SIM)模式检测,以保留时间和特征离子丰度比定性,稳定同位素稀释内标法定量。在优化的实验条件下,5种磷酸三酯类化合物在各自的线性范围内相关系数大于0.9995,方法检出限为1.0~30μg/kg,平均回收率为89.5%~105%,相对标准偏差(n=6)为2.9%~9.1%。本方法净化效果好,可有效消除基质效应,且有较好的回收率,可用于不同类型的化妆品基质中磷酸三酯类化合物的测定。
根據不同化妝品的基質特性探討優化不同的提取淨化方法,建立瞭穩定同位素稀釋氣相色譜-質譜聯用測定化妝品中5種燐痠三酯類化閤物( OPEs)的方法。膏霜乳液類和蠟基類化妝品經溶劑提取後,採用ENVI-Carb固相萃取柱淨化;粉劑類和水劑類化妝品經溶劑提取、濃縮後直接檢測。樣液經DB-5MS(30 m×0.25 mm×0.25μm)色譜柱分離,GC-MS的選擇離子鑑測( SIM)模式檢測,以保留時間和特徵離子豐度比定性,穩定同位素稀釋內標法定量。在優化的實驗條件下,5種燐痠三酯類化閤物在各自的線性範圍內相關繫數大于0.9995,方法檢齣限為1.0~30μg/kg,平均迴收率為89.5%~105%,相對標準偏差(n=6)為2.9%~9.1%。本方法淨化效果好,可有效消除基質效應,且有較好的迴收率,可用于不同類型的化妝品基質中燐痠三酯類化閤物的測定。
근거불동화장품적기질특성탐토우화불동적제취정화방법,건립료은정동위소희석기상색보-질보련용측정화장품중5충린산삼지류화합물( OPEs)적방법。고상유액류화사기류화장품경용제제취후,채용ENVI-Carb고상췌취주정화;분제류화수제류화장품경용제제취、농축후직접검측。양액경DB-5MS(30 m×0.25 mm×0.25μm)색보주분리,GC-MS적선택리자감측( SIM)모식검측,이보류시간화특정리자봉도비정성,은정동위소희석내표법정량。재우화적실험조건하,5충린산삼지류화합물재각자적선성범위내상관계수대우0.9995,방법검출한위1.0~30μg/kg,평균회수솔위89.5%~105%,상대표준편차(n=6)위2.9%~9.1%。본방법정화효과호,가유효소제기질효응,차유교호적회수솔,가용우불동류형적화장품기질중린산삼지류화합물적측정。
A method based on stable isotope dilution gas chromatography-mass spectrometry ( GC-MS ) was established to determine five kinds of organophosphate esters ( OPEs ) in different kinds of cosmetics. For cream and wax-based cosmetics, samples were extracted by appropriate solvent, and then purified by ENVI-Carb solid phase extracting column. For powder and aqueous samples, GC-MS test could be operated directly after solvent extraction and concentration. All of the samples were separated by DB-5MS (30 m×0. 25 mm× 0. 25 μm) chromatographic column, and detected by selected ion monitoring ( SIM ) mode. The target analytes were qualitatively confirmed by retention time and abundance ratio of characteristic ions, and quantified by stable isotope diluted internal standard method. Under the optimized conditions, the linear coefficients of the OPEs were larger than 0. 9995, the detection limits were 1. 0-30 μg/kg, the average recoveries ( n=6 ) ranged from 89 . 5% to 105%, and the RSDs were in the range of 2 . 9%-9 . 1%. The developed method, which was characteristic by satisfactory purification effect, favorable matrix effect elimination capacity, as well as high recovery, was suitable for the determination of OPEs in different kinds of cosmetic matrices.