TY - JOUR
T1 - Development of a robust, fast screening method for the potentiometric determination of iodide in urine and salt samples
AU - Machado, Ana
AU - Mesquita, Raquel B. R.
AU - Oliveira, Sara
AU - Bordalo, Adriano A.
PY - 2017/5/15
Y1 - 2017/5/15
N2 - In this work, a potentiometric flow injection method is described for the fast bi-parametric determination of iodide and iodate in urine and salt samples. The developed methodology aimed for iodine speciation with a potentially portable system (running on batteries). The iodate reduction to iodide was effectively attained in line within the same manifold. The iodide determination was accomplished in the dynamic range of 2.50×10−6–1.00×10−3 M and the total iodine dynamic range, resulted from iodide plus iodate, was 3.50×10−6–2.00×10−3 M. The calculated limits of detection were 1.39×10−6 M and 1.77×10−6 M for iodide and iodate, respectively. A determination rate of 21 h−1 for the bi-parametric iodide and iodate determination was obtained for sample injection. The urine samples (RSD <5.8% for iodide and RSD <7.0% for iodate) results were in agreement with those obtained by the classic Sandell-Kolthoff reaction colorimetric reference procedure (RD <7.0%) and standard samples from Centers for Disease Control and Prevention, Atlanta, USA (CDC) international inter-laboratory EQUIP program. The developed flow method was also successfully applied to the iodide and iodate determination in salt samples (RSD <3.1% for iodate and iodide), with comparable results to conventional procedures. No significant interferences were observed interference percentage <9% for both determinations.
AB - In this work, a potentiometric flow injection method is described for the fast bi-parametric determination of iodide and iodate in urine and salt samples. The developed methodology aimed for iodine speciation with a potentially portable system (running on batteries). The iodate reduction to iodide was effectively attained in line within the same manifold. The iodide determination was accomplished in the dynamic range of 2.50×10−6–1.00×10−3 M and the total iodine dynamic range, resulted from iodide plus iodate, was 3.50×10−6–2.00×10−3 M. The calculated limits of detection were 1.39×10−6 M and 1.77×10−6 M for iodide and iodate, respectively. A determination rate of 21 h−1 for the bi-parametric iodide and iodate determination was obtained for sample injection. The urine samples (RSD <5.8% for iodide and RSD <7.0% for iodate) results were in agreement with those obtained by the classic Sandell-Kolthoff reaction colorimetric reference procedure (RD <7.0%) and standard samples from Centers for Disease Control and Prevention, Atlanta, USA (CDC) international inter-laboratory EQUIP program. The developed flow method was also successfully applied to the iodide and iodate determination in salt samples (RSD <3.1% for iodate and iodide), with comparable results to conventional procedures. No significant interferences were observed interference percentage <9% for both determinations.
KW - Iodide and iodate bi-parametric determination
KW - Potentiometric detection
KW - Salt samples
KW - Urine samples
UR - http://www.scopus.com/inward/record.url?scp=85014683227&partnerID=8YFLogxK
U2 - 10.1016/j.talanta.2017.03.017
DO - 10.1016/j.talanta.2017.03.017
M3 - Article
C2 - 28340780
AN - SCOPUS:85014683227
SN - 0039-9140
VL - 167
SP - 688
EP - 694
JO - Talanta
JF - Talanta
ER -