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Chip-Based Spectrofluorimetric Determination of Iodine in a Multi-Syringe Flow Platform with and without In-Line Digestion—Application to Salt,Pharmaceuticals, and Algae Samples
Authors:Joana L. A. Miranda,Raquel B. R. Mesquita,Edwin Palacio,José   M. Estela,Ví  ctor Cerdà  ,Antó  nio O. S. S. Rangel
Affiliation:1.CBQF—Centro de Biotecnologia e Química Fina—Laboratório Associado, Escola Superior de Biotecnologia, Universidade Católica Portuguesa, Rua Diogo Botelho 1327, 4169-005 Porto, Portugal; (J.L.A.M.); (R.B.R.M.);2.Department of Chemistry, University of the Balearic Islands, 07122 Palma de Mallorca, Spain; (E.P.); (J.M.E.);3.Sciware Systems S.L., 07193 Bunyola, Spain;
Abstract:In this work, a flow-based spectrofluorimetric method for iodine determination was developed. The system consisted of a miniaturized chip-based flow manifold for solutions handling and with integrated spectrofluorimetric detection. A multi-syringe module was used as a liquid driver. Iodide was quantified from its catalytic effect on the redox reaction between Ce(IV) and As(III), based on the Sandell–Kolthoff reaction. The method was applied for the determination of iodine in salt, pharmaceuticals, supplement pills, and seaweed samples without off-line pre-treatment. An in-line oxidation process, aided by UV radiation, was implemented to analyse some samples (supplement pills and seaweed samples) to eliminate interferences and release iodine from organo-iodine compounds. This feature, combined with the fluorometric reaction, makes this method simpler, faster, and more sensitive than the classic approach of the Sandell–Kolthoff reaction. The method allowed iodine to be determined within a range of 0.20–4.0 µmol L−1, with or without the in-line UV digestion, with a limit of detection of 0.028 µmol L−1 and 0.025 µmol L−1, respectively.
Keywords:iodine, spectrofluorimetry, chip-based manifold, multi-syringe flow system, in-line UV digestion, photooxidation, Sandell–  Kolthoff reaction
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