Meng Xianshuang, Bai Hua, Guo Teng, Niu Zengyuan, Ma Qiang
Chinese Academy of Inspection and Quarantine, Beijing 100176, China.
Thermo Fisher Scientific, Beijing 100102, China.
J Chromatogr A. 2017 Dec 15;1528:61-74. doi: 10.1016/j.chroma.2017.11.004. Epub 2017 Nov 6.
Comprehensive identification and quantitation of 100 multi-class regulated ingredients in cosmetics was achieved using ultra-high-performance liquid chromatography (UHPLC) coupled with hybrid quadrupole-Orbitrap high-resolution mass spectrometry (Q-Orbitrap HRMS). A simple, efficient, and inexpensive sample pretreatment protocol was developed using ultrasound-assisted extraction (UAE), followed by dispersive solid-phase extraction (dSPE). The cosmetic samples were analyzed by UHPLC-Q-Orbitrap HRMS under synchronous full-scan MS and data-dependent MS/MS (full-scan MS/dd-MS) acquisition mode. The mass resolution was set to 70,000 FWHM (full width at half maximum) for full-scan MS and 17,500 FWHM for dd-MS stage with the experimentally measured mass deviations of less than 2ppm (parts per million) for quasi-molecular ions and 5ppm for characteristic fragment ions for each individual analyte. An accurate-mass database and a mass spectral library were built in house for searching the 100 target compounds. Broad screening was conducted by comparing the experimentally measured exact mass of precursor and fragment ions, retention time, isotopic pattern, and ionic ratio with the accurate-mass database and by matching the acquired MS/MS spectra against the mass spectral library. The developed methodology was evaluated and validated in terms of limits of detection (LODs), limits of quantitation (LOQs), linearity, stability, accuracy, and matrix effect. The UHPLC-Q-Orbitrap HRMS approach was applied for the analysis of 100 target illicit ingredients in 123 genuine cosmetic samples, and exhibited great potential for high-throughput, sensitive, and reliable screening of multi-class illicit compounds in cosmetics.
使用超高效液相色谱(UHPLC)与混合四极杆-轨道阱高分辨率质谱(Q-Orbitrap HRMS)联用,实现了对化妆品中100种多类受监管成分的全面鉴定和定量分析。采用超声辅助萃取(UAE),随后进行分散固相萃取(dSPE),开发了一种简单、高效且廉价的样品预处理方案。化妆品样品通过UHPLC-Q-Orbitrap HRMS在同步全扫描质谱和数据依赖型二级质谱(全扫描MS/dd-MS)采集模式下进行分析。全扫描MS的质量分辨率设置为70,000半高宽(FWHM),dd-MS级的质量分辨率设置为17,500 FWHM,每个分析物的准分子离子的实验测量质量偏差小于2ppm(百万分之一),特征碎片离子的质量偏差小于5ppm。内部构建了精确质量数据库和质谱图库,用于搜索100种目标化合物。通过将前体离子和碎片离子的实验测量精确质量、保留时间、同位素模式和离子比率与精确质量数据库进行比较,并将采集的二级质谱图与质谱图库进行匹配,进行了广泛的筛选。根据检测限(LOD)、定量限(LOQ)、线性、稳定性、准确性和基质效应,对所开发的方法进行了评估和验证。UHPLC-Q-Orbitrap HRMS方法应用于123个正品化妆品样品中100种目标非法成分的分析,在高通量、灵敏且可靠地筛选化妆品中多类非法化合物方面显示出巨大潜力。