Key Laboratory of Food Nutrition and Safety, Ministry of Education, Tianjin University of Science and Technology, Tianjin, Tianjin 300457, China.
Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2009 Jun;26(6):839-46. doi: 10.1080/02652030902774631.
A method was developed for the determination of total arsenic in foods using flow injection on-line sorption coupled with hydride generation atomic fluorescence spectrometry (HG-AFS) using a cigarette filter as the sorbent material. After reducing As(V) to As(III) by using L-cysteine, the determination of total arsenic was achieved through on-line formation and retention of the pyrrolidine dithiocarbamate arsenic complex (As(III)-PDC) on the cigarette filter, which was packed in the pre-concentration column and total arsenic was determined by HG-AFS. The analytes were eluted with 1.68 mol l(-1) HCl from the sorbent material. With consumption of 22 ml of the sample solution, an enrichment factor of 25.6 was obtained at a sample throughput of 11.6 h(-1). The detection limits (3 standard deviations) and the precision (relative standard deviation) in foods ranged from 2.5 to 9.9 ng g(-1) and from 1.1 to 2.2%, respectively. The method was used to determine arsenic in carrot, mushroom, chicken tissue, cod fish, rice, common carp and shrimp.
建立了流动注射在线吸附-氢化物发生原子荧光光谱法测定食品中总砷的方法,采用香烟过滤嘴作为吸附材料。用 L-半胱氨酸将 As(V)还原为 As(III)后,通过在线形成和保留在香烟过滤嘴上的吡咯烷二硫代氨基甲酸砷配合物(As(III)-PDC),实现了总砷的测定,该配合物被填充在预浓缩柱中,通过氢化物发生原子荧光光谱法测定总砷。用 1.68 mol/L HCl 从吸附材料中洗脱分析物。在样品溶液消耗 22 ml 的情况下,在 11.6 h-1 的样品通量下获得 25.6 的富集因子。在食品中的检测限(3 倍标准偏差)和精密度(相对标准偏差)范围分别为 2.5 至 9.9 ng/g 和 1.1 至 2.2%。该方法用于测定胡萝卜、蘑菇、鸡肉组织、鳕鱼、大米、鲤鱼和虾中的砷。