Vu Hai Anh, Nguyen Manh Ha, Vu-Thi Hong-An, Do-Hong Quan, Dang Xuan Hoang, Nguyen Thi Ngoc Bich, Trinh Hong Quan, Ly Bich Thuy, Nguyen Tien-Thanh, Le-Van Dung, Tu Minh Binh, Chu Dinh Binh
Faculty of Chemistry, VNU University of Science, Vietnam National University Hanoi, 19 Le Thanh Tong, Hoan Kiem, Hanoi 100000, Vietnam.
Department of Analytical Chemistry, School of Chemical Engineering, Hanoi University of Science and Technology, 1 Dai Co Viet, Hai Ba Trung, Hanoi 100000, Vietnam.
J Anal Methods Chem. 2019 Apr 28;2019:5924942. doi: 10.1155/2019/5924942. eCollection 2019.
In this work, high-performance liquid chromatography in combination with inductively coupled plasma dynamic reaction cell quadrupole mass spectrometry was introduced and optimized for speciation analysis of five major arsenic species including arsenobetain (AsB), arsenite (As(III)), monomethylarsonic (MMA), dimethylarsenonic acid (DMA), and arsenate (As(V)) in rice samples. Five arsenic compounds were separated on a Hamilton PRP X100 strong anion-exchange column employed with the mobile phase that is compatible with mass spectrometry, containing ammonium carbonate, methanol, and disodium ethylenediaminetetraacetic acid. Arsenic compounds were detected online by inductively coupled plasma dynamic reaction cell quadrupole mass spectrometry utilizing oxygen as the reaction gas at a flow rate of 0.7 mL·min. Five selected arsenic species were baseline separated at the optimum experimental conditions. The excellent LOD and LOQ values of the developed method were achieved in the range of 0.5 to 2.9 g·kg and 1.7 to 9.6 g·kg for all species of arsenic, respectively. The ionization effect in plasma during chromatographic gradient elution was systematically investigated by using postcolumn injector. Arsenic compounds in rice samples were extracted by diluted nitric acid at elevated temperature. The extraction efficiency and the interconversion of target compounds during sample preparation were also assessed. The full validation of the developed method was performed by using certified reference material, BRC 211, from European Institute of Reference and Standard for speciation analysis. The recovery of all selected arsenic species was in the range of 70 to 135.5%. The validated method was also applied to analyze rice samples collected from some contaminated rice fields. The results showed that As(III), DMA, and As(V) were found in all rice samples. Average concentration (range) of inorganic arsenic and DMA in all rice samples were 130.3 (65.5-228.1) and 32 (8.2-133.01) g·kg, respectively. However, total concentration of inorganic arsenic in most of investigated rice samples was below the maximum residual level according to US-FDA and European Union standards.
在本研究中,引入并优化了高效液相色谱与电感耦合等离子体动态反应池四极杆质谱联用技术,用于水稻样品中五种主要砷形态的形态分析,这五种砷形态包括砷甜菜碱(AsB)、亚砷酸盐(As(III))、一甲基砷酸(MMA)、二甲基砷酸(DMA)和砷酸盐(As(V))。五种砷化合物在Hamilton PRP X100强阴离子交换柱上分离,流动相为与质谱兼容的含碳酸铵、甲醇和乙二胺四乙酸二钠的溶液。砷化合物通过电感耦合等离子体动态反应池四极杆质谱在线检测,以氧气作为反应气,流速为0.7 mL·min⁻¹。在最佳实验条件下,五种选定的砷形态实现了基线分离。所建立方法的检出限(LOD)和定量限(LOQ)表现优异,所有砷形态的检出限在0.5至2.9 μg·kg⁻¹范围内,定量限在1.7至9.6 μg·kg⁻¹范围内。通过柱后进样器系统研究了色谱梯度洗脱过程中等离子体中的电离效应。水稻样品中的砷化合物在高温下用稀硝酸萃取。还评估了样品制备过程中的萃取效率和目标化合物的相互转化。使用欧洲参考与标准研究所的认证参考物质BRC 211对所建立的方法进行了全面验证。所有选定砷形态的回收率在70%至135.5%范围内。该经过验证的方法还应用于分析从一些受污染稻田采集的水稻样品。结果表明,所有水稻样品中均检测到As(III)、DMA和As(V)。所有水稻样品中无机砷和DMA的平均浓度(范围)分别为130.3(65.5 - 228.1)μg·kg⁻¹和32(8.2 - 133.01)μg·kg⁻¹。然而,根据美国食品药品监督管理局(US - FDA)和欧盟标准,大多数调查水稻样品中无机砷的总浓度低于最大残留限量。