Departamento de Química Analítica y Alimentaria, Área de Química Analítica, Facultad de Química, Universidad de Vigo, As Lagoas-Marcosende s/n, 36310 Vigo, Spain.
Anal Chim Acta. 2010 Oct 29;679(1-2):49-55. doi: 10.1016/j.aca.2010.09.004. Epub 2010 Sep 15.
In this work, the determination of rare earth elements (REEs), i.e. Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu in marine biological tissues by inductively coupled-mass spectrometry (ICP-MS) after a sample preparation method based on ultrasound-assisted extraction (UAE) is described. The suitability of the extracts for ICP-MS measurements was evaluated. For that, studies were focused on the following issues: (i) use of clean up of extracts with a C18 cartridge for non-polar solid phase extraction; (ii) use of different internal standards; (iii) signal drift caused by changes in the nebulization efficiency and salt deposition on the cones during the analysis. The signal drift produced by direct introduction of biological extracts in the instrument was evaluated using a calibration verification standard for bracketing (standard-sample bracketing, SSB) and cumulative sum (CUSUM) control charts. Parameters influencing extraction such as extractant composition, mass-to-volume ratio, particle size, sonication time and sonication amplitude were optimized. Diluted single acids (HNO(3) and HCl) and mixtures (HNO(3)+HCl) were evaluated for improving the extraction efficiency. Quantitative recoveries for REEs were achieved using 5 mL of 3% (v/v) HNO(3)+2% (v/v) HCl, particle size <200 μm, 3 min of sonication time and 50% of sonication amplitude. Precision, expressed as relative standard deviation from three independent extractions, ranged from 0.1 to 8%. In general, LODs were improved by a factor of 5 in comparison with those obtained after microwave-assisted digestion (MAD). The accuracy of the method was evaluated using the CRM BCR-668 (mussel tissue). Different seafood samples of common consumption were analyzed by ICP-MS after UAE and MAD.
在这项工作中,描述了一种基于超声辅助提取(UAE)的样品制备方法,通过电感耦合质谱(ICP-MS)测定海洋生物组织中的稀土元素(REEs),即 Y、La、Ce、Pr、Nd、Sm、Eu、Gd、Tb、Dy、Ho、Er、Tm、Yb 和 Lu。评估了提取物用于 ICP-MS 测量的适用性。为此,研究集中在以下几个问题上:(i)使用 C18 柱对提取物进行非极性固相萃取的净化;(ii)使用不同的内标;(iii)分析过程中雾化效率变化和锥体盐沉积引起的信号漂移。通过使用标准-样品内标(SSB)和累积和(CUSUM)控制图对仪器中直接引入生物提取物引起的信号漂移进行了评估。优化了萃取参数,如萃取剂组成、质量与体积比、粒径、超声时间和超声幅度。评估了稀释的单酸(HNO3 和 HCl)和混合物(HNO3+HCl)以提高萃取效率。使用 5 mL 3%(v/v)HNO3+2%(v/v)HCl、粒径<200 μm、超声时间 3 min 和超声幅度 50%,实现了 REEs 的定量回收。精密度以三个独立萃取的相对标准偏差表示,范围为 0.1 至 8%。与微波辅助消解(MAD)后获得的结果相比,一般情况下,LOD 提高了 5 倍。使用 CRM BCR-668(贻贝类组织)评估了该方法的准确性。通过 ICP-MS 分析了不同的常见消费海鲜样品,分别采用 UAE 和 MAD 两种方法。