A simple dilute-and-shoot approach for the determination of ultra-trace levels of arsenic in biological fluids via ICP-MS using CH3F/He as a reaction gas. Issue 1 (30th October 2015)

• Record Type: Journal Article
• Authors: Flórez, M. R.; García-Ruiz, E.; Bolea-Fernández, E.; Vanhaecke, F.; Resano, M.
• Is Part Of: Journal of analytical atomic spectrometry. Volume 31:Issue 1(2016:Jan.)
• Page Start: 245
• Page End: 251
• Publication Date: 2015-10-30
• Subjects: Atomic spectra -- Periodicals; Atomic absorption spectroscopy -- Periodicals; 543.0858
• DOI: 10.1039/c5ja00298b
• Languages: English
• ISSNs: 0267-9477

Abstract

Abstract : This article demonstrates the potential of CH3 F as a reaction gas for the interference-free monitoring of As by ICP-MS. Abstract : The performance of a mixture of CH3 F/He (1/9) as a reaction gas for the determination of As in biological fluids using a quadrupole ICP-MS instrument has been explored. A simple (dilute-and-shoot) interference-free method has been developed to quantify As concentrations at trace and ultra-trace levels in matrices with a high Cl content. As + reacts with CH3 F (through CH3 F addition, followed by HF elimination) with high efficiency forming AsCH2 + as the primary reaction product, which can be monitored at a mass-to-charge ratio of 89, free from the Cl-based interferents ( e.g., 40 Ar 35 Cl + and 40 Ca 35 Cl + ) that hamper the monitoring of 75 As + . Matrix effects are overcome by the use of Te as an internal standard and the addition of 3% v/v ethanol to all samples and calibration standard solutions. The method presented was validated by analysing a set of reference materials (blood, serum and urine) and by assessing As recovery from a set of real blood samples. With this method, the limit of detection was calculated to be 0.8 ng L −1 As, favourably comparable to the vast majority of values reported in the literature, even with those obtained using more sophisticated sector-field instrumentation.