Yang Ming, Tian Shili, Liu Qingyang, Yang Zheng, Yang Yifan, Shao Peng, Liu Yanju
Institute of Analysis and Testing, Beijing Academy of Science and Technology (Beijing Center for Physical and Chemical Analysis), Beijing 100089, China.
College of Biology and the Environment, Nanjing Forestry University, Nanjing 210037, China.
Toxics. 2022 Oct 22;10(11):634. doi: 10.3390/toxics10110634.
The method for the determination of 16 priority polycyclic aromatic hydrocarbons (PAHs) in plant leaves has been studied extensively, yet the quantitativemethod for measuring non-priority PAHs in plant leaves is limited. A method for the simultaneous determination of 31 polycyclic aromatic hydrocarbons (PAHs) in plant leaves was established using an ultrasonic extraction-gas chromatography-mass spectrometry-internal standard method. The samples of plant leaves were extracted with ultrasonic extraction and purified with solid-phase extraction columns. The PAHs were separated by using gas chromatography-mass spectrometry equipped with a DB-EUPAH capillary column (20 m × 0.18 mm × 0.14 μm) with a selective ion monitoring (SIM) detection mode, and quantified with an internal standard. The method had good linearity in the range of 0.0051.0 μg/mL with correlation coefficients greater than 0.99, and the method detection limit and maximum quantitative detection limit were in the ranges of 0.20.7 μg/kg and 0.8~2.8 μg/kg, respectively. The method was verified with spiked recovery experiments. The average spiked recovery ranged from 71.0% to 97.6% and relative standard deviations ( = 6) were less than 14%. Herein, we established a quantitativemethod for the simultaneous determination of priority and non-priority PAHs in plant leaves using GC-MS. The method is highly sensitive and qualitatively accurate, and it is suitable for the determination of PAHs in plant leaves.
植物叶片中16种优先多环芳烃(PAHs)的测定方法已得到广泛研究,但植物叶片中非优先PAHs的定量测定方法有限。采用超声萃取-气相色谱-质谱-内标法建立了同时测定植物叶片中31种多环芳烃(PAHs)的方法。植物叶片样品经超声萃取后,用固相萃取柱净化。PAHs采用配备DB-EUPAH毛细管柱(20 m×0.18 mm×0.14μm)的气相色谱-质谱仪,在选择离子监测(SIM)检测模式下进行分离,并用内标法定量。该方法在0.0051.0μg/mL范围内具有良好的线性,相关系数大于0.99,方法检出限和最大定量检出限分别在0.20.7μg/kg和0.82.8μg/kg范围内。通过加标回收实验对该方法进行了验证。平均加标回收率在71.0%97.6%之间,相对标准偏差(n = 6)小于14%。在此,我们建立了一种使用气相色谱-质谱同时测定植物叶片中优先和非优先PAHs的定量方法。该方法灵敏度高、定性准确,适用于植物叶片中PAHs的测定。