Su Z J, Hu S G, Cai W H, Yang X F, Wang J, Fan J B, Huang H Y, Huang W X
Department of inspection, Centre for Disease Control and Prevention of Guangdong, Guangzhou 510300, China.
Zhonghua Yu Fang Yi Xue Za Zhi. 2018 Oct 6;52(10):994-1002. doi: 10.3760/cma.j.issn.0253-9624.2018.10.006.
A new ion exchange column technology was used to establish an efficient and sensitive method for the detection of inorganic arsenic. Based on the new As Specia Fast Column, the pretreatment methods, liquid phase separation and mass spectrometry determination conditions of inorganic arsenic in rice were optimized. Finally, arsenic compounds were separated by As Specia Fast Column and detected by liquid chromatography inductively coupled plasma mass spectrometry. The external standard method was used for quantitative analysis. The detection limit, precision and accuracy of the method were determined by measuring the content of arsenic compounds in rice samples and rice standard samples. At the same time, three Guangdong rice samples were selected as the experimental samples of this study, and 1 g of each sample was weighed and measured in parallel three times. The method was compared with the method of liquid chromatography-atomic fluorescence spectrometry (LC-AFS) and liquid chromatography-inductively coupled plasma mass spectrometry (LC-ICP-MS) in the national standard. The inorganic arsenic in rice was extracted with 0.5% nitric acid solution at 65 ℃ for 15 h, and the pH was adjusted to alkaline. The mobile phase A (8 mmol/L HNO(3), 50 mmol/L NH(3)·H(2)O) and mobile phase B (40 mmol/L HNO(3), 80 mmol/L NH(3)·H(2)O) were used as the mobile phase gradient elution (93%) . Five arsenic compounds can reach baseline separation under the conditions of RF power of 1 500 W and atomization gas flow of 0.97 L/min. The detection limits ranged from 0.114 to 0.331 μg/L, and the inorganic arsenic content in rice samples ranged from 0.063 to 0.232 mg/kg. The results of determination of arsenic compounds in rice flour reference materials were all within the uncertainty range indicated by the standard. The recoveries were 86.7%~106.7%, and the precision was 1.9%-12.5%. Compared with national standards, the results of determination of arsenate in rice were relatively close (using this method, LC-AFS, LC-ICP-MS to detect the content of arsenate in rice samples 1 was 0.231, 0.226, 0.236 mg/kg, respectively). However, due to insufficient sensitivity, the national standard method is difficult to detect low levels of arsenic compounds (Arsenobetaine was not detected in rice sample 1). The method can detect the content of arsenobetaine in rice sample 1 was 0.023 mg/kg. The established method can meet the requirements of inorganic arsenic determination in rice, and it is more rapid and accurate than the current national standard. It can better monitor and evaluate the content of i-As in rice, and provide accurate data for comprehensively grasping and evaluating the safety of rice consumption of residents.
采用一种新型离子交换柱技术建立了一种高效、灵敏的无机砷检测方法。基于新型As Specia Fast柱,对大米中无机砷的预处理方法、液相分离及质谱测定条件进行了优化。最终,通过As Specia Fast柱分离砷化合物,并采用液相色谱 - 电感耦合等离子体质谱法进行检测。采用外标法进行定量分析。通过测定大米样品和大米标准样品中砷化合物的含量,确定了该方法的检出限、精密度和准确度。同时,选取3个广东大米样品作为本研究的实验样品,每个样品称取1 g,平行测定3次。将该方法与国家标准中的液相色谱 - 原子荧光光谱法(LC - AFS)和液相色谱 - 电感耦合等离子体质谱法(LC - ICP - MS)进行比较。大米中的无机砷用0.5%硝酸溶液在65℃下提取15 h,并将pH值调至碱性。以流动相A(8 mmol/L HNO₃,50 mmol/L NH₃·H₂O)和流动相B(40 mmol/L HNO₃,80 mmol/L NH₃·H₂O)作为流动相进行梯度洗脱(93%)。在射频功率为1500 W、雾化气流速为0.97 L/min的条件下,5种砷化合物可实现基线分离。检出限为0.114~0.331 μg/L,大米样品中无机砷含量为0.063~0.232 mg/kg。米粉标准物质中砷化合物的测定结果均在标准规定的不确定度范围内。回收率为86.7%~106.7%,精密度为1.9% - 12.5%。与国家标准相比,大米中砷酸盐的测定结果较为接近(采用本方法、LC - AFS、LC - ICP - MS检测大米样品1中砷酸盐的含量分别为0.231、0.226、0.236 mg/kg)。然而,由于灵敏度不足,国家标准方法难以检测低含量的砷化合物(大米样品1中未检测到砷甜菜碱)。本方法可检测大米样品1中砷甜菜碱的含量为0.023 mg/kg。所建立的方法能够满足大米中无机砷测定的要求,比现行国家标准更快速、准确。能够更好地监测和评价大米中无机砷的含量,为全面掌握和评价居民大米消费安全性提供准确数据。