Next-generation rapid serum tube technology using prothrombin activator coagulant: fast, high-quality serum from normal samples

Author:

Zhao Kong-Nan12,Dimeski Goce34,de Jersey John4,Johnson Lambro A.1,Grant Michael5,Masci Paul P.12,Lavin Martin F.6

Affiliation:

1. Centre for Venomics Research, School of Medicine , The University of Queensland, Translational Research Institute , Woolloongabba, QLD , Australia

2. Centre for Clinical Research, The University of Queensland, Royal Brisbane and Women’s Hospital Campus , Herston, Brisbane, QLD , Australia

3. Chemical Pathology, Princess Alexandra Hospital , Woolloongabba, Brisbane, QLD , Australia

4. School of Chemistry and Molecular Biosciences , The University of Queensland, Brisbane , QLD , Australia

5. Q-Sera Pty Ltd , Melbourne, VIC , Australia

6. Centre for Clinical Research, The University of Queensland, Royal Brisbane and Women’s Hospital Campus , Herston, Brisbane, QLD 4029 , Australia , Phone: +61 07 3346 6045, Fax: +61 07 3346 5509

Abstract

Abstract Background Incomplete blood clotting or latent clotting in serum is a common laboratory problem, especially for patients on anticoagulant therapy or when serum tubes are centrifuged before clotting is completed. We describe a novel approach to producing high-quality serum using snake venom prothrombin activator complex (OsPA) as an additive in blood collection tubes for non-anticoagulated (normal) individuals. Methods Plasma clotting assays were performed using a Hyland-Clotek instrument. Blood clotting was visually observed, and thromboelastography was also performed to determine the important parameters of coagulation. Thrombin generation was assayed using the chromogenic substrate S-2238, and biochemical analytes in the serum were determined on chemistry and immunoassay analysers. Fibrinogen was determined by either ELISA or Clauss fibrinogen assay. Results We initially showed that OsPA had strong coagulation activity in clotting not only recalcified citrated plasma and recalcified citrated whole blood, but also fresh whole blood in a clinical setting. The use of TEG clearly showed improved speed of clotting and generation of a firmer clot. We also showed that the use of OsPA to produce serum did not interfere with the determination of commonly measured biochemical analytes. The underlying clotting mechanism involves a burst of thrombin production at the initial stages of the clotting process upon contact with prothrombin in blood. Conclusions These results demonstrate rapid generation of high-quality serum, contributing to faster turnaround times with standardised quality samples, for accurate analyte determinations in normal individuals.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry, medical,Clinical Biochemistry,General Medicine

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