超高效液相色谱-四级杆/静电场轨道阱高分辨质谱法高通量筛查化妆品中157种非法添加化学药物

    High-throughput Screening of 157 Illegally Added Chemical Drugs in Cosmetic by UPLC-Q/Exactive Orbitrap HRMS

    • 摘要:
      目的 基于超高效液相色谱-四级杆/静电场轨道阱高分辨质谱法(UPLC-Q/Exactive Orbitrap HRMS),建立化妆品中157种非法添加化学药物的高通量筛查方法。
      方法 根据目标物性质差异采用不同的前处理,对于1~123#目标物,样品经乙腈超声提取后,分别进行衍生化(环比酮胺)、甲醇稀释(他克莫司和吡美莫司)或0.4%甲酸溶液稀释(其余成分)处理,采用ACQUITY UPLC BEH C18(2.1 mm×100 mm,1.7 μm) 色谱柱分离,分别以0.1%甲酸溶液-乙腈、0.1%乙酸-5 mmol乙酸铵溶液-甲醇、水-乙腈为流动相进行梯度洗脱。对于124~157#目标物,样品采用20%乙腈溶液超声提取并经正己烷萃取净化后,采用ACQUITY UPLC HSS T3(2.1 mm×100 mm,1.8 μm) 色谱柱分离,以0.1%甲酸溶液-乙腈为流动相进行梯度洗脱。流速为 0.3 mL·min–1,122~123#柱温为40 ℃,其余成分30 ℃。进样量为2 μL。采用加热电喷雾离子源(HESI),在正离子和负离子模式下,以全扫描/数据依赖二级质谱扫描(Full MS/dd-MS2)模式进行数据采集,获得各化合物的保留时间、一级母离子及二级特征碎片离子精确质量数,利用TraceFinder 软件构建157种非法添加化学药物的筛查数据库。
      结果 应用所建方法对107批市售化妆品进行筛查,其中1批儿童护肤产品检出特比萘芬,1批祛痘产品检出呋喃西林。
      结论 该方法灵敏度高,特异性好,检测效率高,实验成本低,适用于化妆品中非法添加药物的高通量筛查,为化妆品安全监管提供技术支撑。

       

      Abstract:
      OBJECTIVE To establish a method for the high-throughput screening of 157 illegal chemical drugs in cosmetics by ultra-performance liquid chromatography-quadrupole/electrostatic field orbitrap high resolution mass spectrometry(UPLC-Q/Exactive Orbitrap HRMS).
      METHODS Different pretreatment were applied according to the properties of the analytes: For components No.1–123, samples were ultrasonically extracted with acetonitrile, followed by derivatization(for cyclopirox olamine), dilution with methanol(for tacrolimus and pimecrolimus), or dilution with 0.4% formic acid solution(for other compounds). Separation was performed on an ACQUITY UPLC BEH C18 column(2.1 mm×100 mm,1.7 μm) with a gradient elution using the following mobile phases, respectively: 0.1% formic acid solution-acetonitrile, 0.1% acetic acid-5 mmol ammonium acetate solution-methanol, and water-acetonitrile. For compounds No.124–157, samples were ultrasonically extracted with 20% acetonitrile solution and purified by n-hexane extraction, followed by separation on an ACQUITY UPLC HSS T3 column(2.1 mm×100 mm, 1.8 μm) with the mobile phase consisting of 0.1% formic acid-acetonitrile in gradient elution . The flow rate was 0.3 mL·min–1, the column temperature was 40 ℃ for compounds No.122–123, and 30 ℃ for other analytes. The injection volume was 2 μL. The retention time, accurate masses of precursor ions, and characteristic fragment ions were obtained in both positive and negative ionization modes using a heated electrospray ionization(HESI) source with full-scan/data-dependent MS2(Full MS/dd-MS2) mode. The TraceFinder software was used to establish a screening database for the 157 illegally added chemical drugs.
      RESULTS Using this method, 107 batches of commercially available cosmetics were screened. Terbinafine was detected in one batch of children’s skincare products, and nitrofurazone was identified in one batch of acne treatment products.
      CONCLUSION The method has high sensitivity, excellent specificity, high detection efficiency, and low experimental cost. It is suitable for high-throughput screening of illegally added drugs in cosmetics and provides technical support for cosmetic safety regulation.

       

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