Page 71 - 理化检验-化学分册2025年第三期
P. 71
王 璐,等:QuEChERS结合超高压液相色谱-三重四极杆串联质谱法测定化妆品中5种禁用组分的含量
961-964. 来酸氯苯那敏的溶出度[J]. 中南药学,2016,14(6):
XU Q Q,DU L M,CAO X M. Simultaneous 655-658.
determination of 8 kinds of components in cannabis, DENG Q J,LIU Y,SHI X Y,et al. HPLC determination
opium and heroine by gas chromatography[J]. Chinese of the dissolution of methoxyphenamine hydrochloride,
Journal of Analytical Chemistry,2003,31(8): aminophylline,narcotin,chlorprophenpyridamine maleate
961-964. in compound methoxyphenamine capsules[J]. Central
[9] 邓晓云,刘志斌. 高效液相色谱法测定复方感冒片 South Pharmacy,2016,14(6):655-658.
中那可丁的含量[J]. 广东药学院学报,2001,17(2): [11] 曾广丰,谢建军,王志元,等. 气相色谱-四极杆/飞行
115-116. 时间质谱法非靶向快速筛查凉茶中的农药残留[J]. 中
DENG X Y,LIU Z B. Determination of narcotine in 国食品学报,2022,22(5):338-347.
compound Ganmao Tablets by HPLC[J]. Academic ZENG G F,XIE J J,WANG Z Y,et al. Non-
Journal of Guangdong College of Pharmacy,2001,17(2): target screening of pesticide residues in herbal tea by
115-116. gas chromatography-quadrupole-time of flight mass
[10] 邓巧君,刘轶,石笑弋,等. 高效液相色谱法测定复方 spectrometry[J]. Journal of Chinese Institute of Food
甲氧那明胶囊中盐酸甲氧那明、氨茶碱、那可丁和马 Science and Technology,2022,22(5):338-347.
Determination of 5 Prohibited Components in Cosmetics by Ultra-High Pressure
Liquid Chromatography-Triple Quadrupole Tandem Mass Spectrometry
Combined with QuEChERS
WANG Lu, CAI Cuiling, DONG Jie, HOU Yingye, ZENG Guangfeng, XIE Jianjun *
(1. Guangzhou Customs Technical Center, Guangzhou 510623,China; 2. National Import and Export Food Quality Safety Risk
Verification and Evaluation Laboratory (Cosmetics), Guangzhou 510623, China)
Abstract: The method mentioned by the title was proposed for simultaneous determination of 5 prohibited components
including cyclophosphamide, azacyclonol, aminopentamide, narcotine and metyrapene in different cosmetic matrices. The samples
of water emulsion and essential oil cosmetics were extracted with methanol, and the samples of cream cosmetics were dispersed
with saturated sodium chloride solution and extracted with anhydrous ethanol. Then both were purified with octadecyl silane boned
silica gel (C 18 ). The targets were separated on Waters BEH C 18 column using a mixed solution of 0. 1% (volume fraction) formic
acid solution and acetonitrile at different volume ratios as the mobile phase for gradient elution. Multiple reaction monitoring (MRM)
mode in mass spectrometry analysis was carried out under positive ion mode of electrospray ion source, and matrix matching
method was used for quantitative analysis. As shown by the results, linear relationships between the corresponding peak areas
− 1
and mass concentrations of 5 prohibited components were found in the range of 5-200 μg · L , with detection limits (3S/N)
in the range of 5-100 μg · kg −1 . Test for recovery at 3 concentration levels was conducted in different blank matrices, and the
recoveries of 5 prohibited components ranged from 90. 1% to 115%, with RSDs (n=6) of the determined values in the range of
2. 0%-14%.
Keywords: QuEChERS; ultra-high pressure liquid chromatography-triple quadrupole tandem mass spectrometry ; cosmetic;
prohibited component
• 305 •

