Letter

A method for detection and quantification of hydroxyethyl starch in plasma

Gordon P Otto1,2*, Bianka Wissuwa1,3, Anne Mehnert1, Sascha Marx1, Michael Raessler4, Wolfgang Lösche1,3, Ralf A Claus1,3 and Maik Sossdorf1,3

Author Affiliations

1 Clinic for Anesthesiology and Intensive Care, Jena University Hospital, Erlanger Allee 101, 07747 Jena, Germany

2 Clinic for Internal Medicine (KIM III) - Nephrology, 07747 Jena University Hospital, Jena, Germany

3 Center for Sepsis Control and Care (CSCC), Jena University Hospital, 07747 Jena, Germany

4 Max-Planck-Institut fuer Biogeochemie, Hans-Knöll-Str. 10, 07745 Jena, Germany

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Critical Care 2012, 16:426 doi:10.1186/cc11302

Published: 8 May 2012

First paragraph (this article has no abstract)

The use of hydroxyethylstarch (HES) is a controversial issue due to increasing evidence that HES accumulates in plasma and various tissues and therefore leads to unfavourable outcome in critically ill patients [1,2]. No simple methods are available for monitoring HES plasma levels; present technologies to measure HES are based on gas chromatography-mass spectrometry, which are time-consuming and need advanced equipment [3]. Here, we applied Lugol's iodine solution (LUGOL; Sigma-Aldrich, Steinheim, Germany) to determinate HES concentrations in plasma and compare the results with those obtained by high-performance liquid chromatography (HPLC).