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采用固体进样热分解/汞齐化原子吸收光谱法测定鲜鱼和鲜虾样品中汞含量的方法验证

Method validation for control determination of mercury in fresh fish and shrimp samples by solid sampling thermal decomposition/amalgamation atomic absorption spectrometry.

作者信息

Torres Daiane Placido, Martins-Teixeira Maristela Braga, Cadore Solange, Queiroz Helena Müller

机构信息

a Brazilian Agricultural Research Corporation , Embrapa Temperate Agriculture , Pelotas , Rio Grande do Sul , Brazil.

出版信息

J Environ Sci Health B. 2015;50(7):514-22. doi: 10.1080/03601234.2015.1018764.

Abstract

A method for the determination of total mercury in fresh fish and shrimp samples by solid sampling thermal decomposition/amalgamation atomic absorption spectrometry (TDA AAS) has been validated following international foodstuff protocols in order to fulfill the Brazilian National Residue Control Plan. The experimental parameters have been previously studied and optimized according to specific legislation on validation and inorganic contaminants in foodstuff. Linearity, sensitivity, specificity, detection and quantification limits, precision (repeatability and within-laboratory reproducibility), robustness as well as accuracy of the method have been evaluated. Linearity of response was satisfactory for the two range concentrations available on the TDA AAS equipment, between approximately 25.0 and 200.0 μg kg(-1) (square regression) and 250.0 and 2000.0 μg kg(-1) (linear regression) of mercury. The residues for both ranges were homoscedastic and independent, with normal distribution. Correlation coefficients obtained for these ranges were higher than 0.995. Limits of quantification (LOQ) and of detection of the method (LDM), based on signal standard deviation (SD) for a low-in-mercury sample, were 3.0 and 1.0 μg kg(-1), respectively. Repeatability of the method was better than 4%. Within-laboratory reproducibility achieved a relative SD better than 6%. Robustness of the current method was evaluated and pointed sample mass as a significant factor. Accuracy (assessed as the analyte recovery) was calculated on basis of the repeatability, and ranged from 89% to 99%. The obtained results showed the suitability of the present method for direct mercury measurement in fresh fish and shrimp samples and the importance of monitoring the analysis conditions for food control purposes. Additionally, the competence of this method was recognized by accreditation under the standard ISO/IEC 17025.

摘要

为了符合巴西国家残留控制计划,已按照国际食品协议对采用固体进样热分解/汞齐化原子吸收光谱法(TDA AAS)测定鲜鱼和鲜虾样品中总汞的方法进行了验证。根据有关食品验证和无机污染物的具体法规,先前已对实验参数进行了研究和优化。评估了该方法的线性、灵敏度、特异性、检测限和定量限、精密度(重复性和实验室内部再现性)、稳健性以及准确性。对于TDA AAS设备上可用的两个浓度范围,汞含量在约25.0至200.0 μg kg⁻¹(平方回归)和250.0至2000.0 μg kg⁻¹(线性回归)之间时,响应线性令人满意。两个范围的残留均为同方差且独立,呈正态分布。这些范围获得的相关系数均高于0.995。基于低汞样品的信号标准偏差(SD),该方法的定量限(LOQ)和检测限(LDM)分别为3.0和1.0 μg kg⁻¹。该方法的重复性优于4%。实验室内部再现性的相对标准偏差优于6%。评估了当前方法的稳健性,指出样品质量是一个重要因素。基于重复性计算了准确性(以分析物回收率评估),范围为89%至99%。所得结果表明本方法适用于直接测定鲜鱼和鲜虾样品中的汞,以及监测食品控制目的分析条件的重要性。此外,该方法的能力已通过ISO/IEC 17025标准的认可。

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