Quantification of heparin in complex matrices (including urine) using a mix-and-read fluorescence assay

Heparin is an important anticoagulant drug, about one billion doses are produced annually. It is a polydisperse sulfated polysaccharide, and the inherent heterogeneity makes the analysis of heparin difficult. The global crisis resulting from adulterated heparin in 2008 has drawn renewed attention to the challenges that are associated with the quality control and characterization of this complex biological medicine from natural sources. The present study addresses the need for simple and user-friendly analytical methods for the fast and accurate quantification of heparin in complex matrices. Direct quantification of heparin in the low microgram per mL range was accomplished using a specific commercially available assay based on the fluorescent molecular probe Heparin Red, simply by mixing the heparin containing sample and a reagent solution in a 96-well microplate followed by fluorescence readout. A screening of typical impurities in raw heparin (selected other glycosaminoglycans, residual nucleic acids and proteins), related to the extraction from animal tissues, as well as of components of the urine matrix (inorganic salts, amino acids, trace proteins) revealed that these compounds even in large excess have no or very little effect on the accuracy of heparin determination. Heparin spike detection in urine, a biological multicomponent matrix, also showed good accuracy. We envision applications of this mix-and-read assay in the process and quality control in heparin manufacturing, but also in pharmacokinetic studies as a convenient tool for measuring of the urinary excretion of heparins.
Comment: Article, 16 pages, 7 figures