Simultaneous Determination of 15 Prohibited Nitroimidazoles in 4 Matrixes of Cosmetics by High Performance Liquid Chromatography-Tandem Mass Spectrometry with QuEChERS Extraction
|更新时间:
|
Simultaneous Determination of 15 Prohibited Nitroimidazoles in 4 Matrixes of Cosmetics by High Performance Liquid Chromatography-Tandem Mass Spectrometry with QuEChERS Extraction
Vol. 38, Issue 11, Pages: 1285-1293(2019)
作者机构:
浙江省食品药品检验研究院
作者简介:
基金信息:
DOI:
CLC:
扫 描 看 全 文
Simultaneous Determination of 15 Prohibited Nitroimidazoles in 4 Matrixes of Cosmetics by High Performance Liquid Chromatography-Tandem Mass Spectrometry with QuEChERS Extraction. [J]. 38(11):1285-1293(2019)
DOI:
Simultaneous Determination of 15 Prohibited Nitroimidazoles in 4 Matrixes of Cosmetics by High Performance Liquid Chromatography-Tandem Mass Spectrometry with QuEChERS Extraction. [J]. 38(11):1285-1293(2019)DOI:
Simultaneous Determination of 15 Prohibited Nitroimidazoles in 4 Matrixes of Cosmetics by High Performance Liquid Chromatography-Tandem Mass Spectrometry with QuEChERS Extraction
A high performance liquid chromatography-tandem mass spectrometric(HPLC-MS/MS) method was developed for the simultaneous determination of 15 prohibited nitroimidazoles(NMZs) in 4 matrixes of cosmetics.Samples were ultrasonically extracted with solvent,and then purified by modified QuEChERS method,filtered through a 0.22 μm microporous membrane.The target compounds were separated on an XSelect CSH C18(2.1 mm×150 mm,3.5 μm) column by gradient elution using acetonitrile solution containing 0.1% formic acid-0.1%formic acid as mobile phase at a flow rate of 0.25 mL/min.The MS/MS analysis was performed with electrospray ion source in positive mode under multiple reaction monitoring(MRM) mode.The matrix matched calibration was used for the quantification.Results showed that there were good linear relationships for 15 nitroimidazoles in the concentration range of 5-500 μg/L with their correlation coefficients(r2) all above 0.99.The limits of detection(LOD) and limits of quantitation(LOQ) were in the ranges of 0.8-200 μg/kg and 4-400 μg/kg,respectively.The recoveries for 15 prohibited drugs at three spiked levels were in the range of 868%-115%with relative standard deviations(RSD) of 0.3%-84%.With simple pretreatment,high separation efficiency and high recovery,the method was suitable for the analysis of nitroimidazoles in cosmetics products.