Related Experiment Video
Updated: Jun 16, 2026

Synthesis and Purification of Iodoaziridines Involving Quantitative Selection of the Optimal Stationary Phase for Chromatography
Published on: May 16, 2014
Urinary Iodine Quantification in Epidemiological Studies: Optimization in Sample Preparation of the Sandell-Kolthoff
Daniel Rosenkranz1, David Vennen1, Antje Kneuer2
1University Institute for Clinical Chemistry and Laboratory Medicine, Oldenburg 26133, Germany.
None:
We present an optimized Sandell-Kolthoff (SK) spectrophotometric method for urinary iodine quantification, developed to enhance analytical accuracy, robustness, and suitability for high-throughput applications while minimizing reagent consumption. A stepwise refinement of an established protocol (Mod 1-4) was performed by adjusting reagent volumes, digestion temperature, and reaction conditions. The final optimized method (Mod 4) demonstrated excellent calibration linearity (r 2 = 0.99964) with a limit of quantification of 10.32 μg/L. Recovery rates for quality controls and certified reference materials ranged from 90 to 105%, with total imprecision (CVtotal) < 3% and analytical bias < 5%. Method comparison with inductively coupled plasma mass spectrometry (ICP-MS) and the Robert Koch Institute (RKI) reference method using Passing-Bablok regression and Bland-Altman analysis confirmed high concordance. Stability testing indicated that iodine concentrations remained unchanged during short-term storage at 4 °C, whereas repeated freeze-thaw cycles caused an average 16% decrease in measured concentrations. Surface contact with urine dipsticks introduced substantial exogenous iodine contamination, resulting in measurement overestimations of up to 45-fold. The optimized SK method provides a validated, precise, and resource-efficient approach for large-scale urinary iodine monitoring, aligning with World Health Organization (WHO) recommendations and addressing key limitations of existing colorimetric protocols.
