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A robust method for testing urinary iodine using a microtitre robotic system.

Ashraf Mina1, Emmanuel J Favaloro, Jerry Koutts

  • 1Department of Endocrinology, Institute of Clinical Pathology and Medical Research (ICPMR), Westmead Hospital, Westmead, New Souh Wales, Australia. ashraf.mina@swahs.health.nsw.gov.au

Journal of Trace Elements in Medicine and Biology : Organ of the Society for Minerals and Trace Elements (GMS)
|October 11, 2011
PubMed
Summary

A new automated method for urinary iodine (UI) testing offers a cheaper, faster, and robust way to screen large populations for iodine deficiency disorders. This advancement improves thyroid hormone production monitoring globally.

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Published on: July 13, 2018

Area of Science:

  • Clinical Chemistry
  • Endocrinology
  • Public Health

Background:

  • Iodine deficiency disorders stem from inadequate thyroid hormone production, affecting an estimated 2 billion people worldwide.
  • Current laboratory assessments include urinary iodine (UI) concentration and various blood markers (FT3, FT4, TSH, Thyroglobulin).

Purpose of the Study:

  • To develop and validate a robust, automated method for urinary iodine concentration testing using a microtitre robotic system.
  • To improve the efficiency and cost-effectiveness of large-scale iodine status assessment.

Main Methods:

  • Automation of the Sandell-Kolthoff reaction, a standard method for iodine measurement, on a microtitre robotic platform.
  • Validation of the automated method against the established manual Sandell-Kolthoff assay through correlation analysis.

Main Results:

  • The automated UI method demonstrated excellent correlation with the manual reference method (r=0.994).
  • Interassay and intraassay variations were comparable to the manual method.
  • Significant cost reductions were achieved due to increased throughput and decreased labor and consumable use.

Conclusions:

  • The automated urinary iodine testing method is a successful adaptation, enabling cheaper, faster, and robust screening for large patient cohorts and populations.
  • The protocol is adaptable to various microtitre robotic systems, capable of processing up to 372 samples per run.