Evidence map›Paper›PMID 38927049›Full record

ArticleBiomolecules2024

Generation of Rapid and High-Quality Serum by Recombinant Prothrombin Activator Ecarin (RAPClot™).

Kong-Nan Zhao, Goce Dimeski, Paul Masci, Lambro Johnson, Jingjing Wang, John de Jersey, Michael Grant, Martin F Lavin

Abstract read
In one paragraph

Article in Biomolecules, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Kong-Nan ZhaoAustralian Institute of Biotechnology and Nanotechnology, The University of Queensland, Brisbane, QLD 4072, Australia.
Goce DimeskiChemical Pathology, Princess Alexandra Hospital, Woolloongabba, Brisbane, QLD 4102, Australia.ORCID 0000-0002-0228-0742
Paul MasciAustralian Institute of Biotechnology and Nanotechnology, The University of Queensland, Brisbane, QLD 4072, Australia.
Lambro JohnsonAustralian Institute of Biotechnology and Nanotechnology, The University of Queensland, Brisbane, QLD 4072, Australia.ORCID 0000-0001-9746-7771
Jingjing WangAustralian Institute of Biotechnology and Nanotechnology, The University of Queensland, Brisbane, QLD 4072, Australia.
John de JerseySchool of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD 4072, Australia.
Michael GrantQ-Sera Pty Ltd., Level 9, 31 Queen St, Melbourne, VIC 3000, Australia.
Martin F LavinAustralian Institute of Biotechnology and Nanotechnology, The University of Queensland, Brisbane, QLD 4072, Australia.

Funding

SOCIAL AND PSYCHOLOGICAL BENEFITS OF EXPERIENCE CORPS PARTICIPATIONP01AG027735 · NIA · JOHNS HOPKINS UNIVERSITY · PI REBOK, GEORGE W. · 2006 to 2013
$10.9M
NIA NIH HHS P01 AG027735
6 · The paper itself

Abstract

We recently reported the potential application of recombinant prothrombin activator ecarin (RAPClot™) in blood diagnostics. In a new study, we describe RAPClot™ as an additive to develop a novel blood collection prototype tube that produces the highest quality serum for accurate biochemical analyte determination. The drying process of the RAPClot™ tube generated minimal effect on the enzymatic activity of the prothrombin activator. According to the bioassays of thrombin activity and plasma clotting, γ-radiation (>25 kGy) resulted in a 30-40% loss of the enzymatic activity of the RAPClot™ tubes. However, a visual blood clotting assay revealed that the γ-radiation-sterilized RAPClot™ tubes showed a high capacity for clotting high-dose heparinized blood (8 U/mL) within 5 min. This was confirmed using Thrombelastography (TEG), indicating full clotting efficiency under anticoagulant conditions. The storage of the RAPClot™ tubes at room temperature (RT) for greater than 12 months resulted in the retention of efficient and effective clotting activity for heparinized blood in 342 s. Furthermore, the enzymatic activity of the RAPClot™ tubes sterilized with an electron-beam (EB) was significantly greater than that with γ-radiation. The EB-sterilized RAPClot™ tubes stored at RT for 251 days retained over 70% enzyme activity and clotted the heparinized blood in 340 s after 682 days. Preliminary clinical studies revealed in the two trials that 5 common analytes (K, Glu, lactate dehydrogenase (LD), Fe, and Phos) or 33 analytes determined in the second study in the γ-sterilized RAPClot™ tubes were similar to those in commercial tubes. In conclusion, the findings indicate that the novel RAPClot™ blood collection prototype tube has a significant advantage over current serum or lithium heparin plasma tubes for routine use in measuring biochemical analytes, confirming a promising application of RAPClot™ in clinical medicine.

Indexed as

Recombinant ProteinsAnticoagulantsBlood CoagulationBlood Specimen CollectionGamma RaysHumansSerumThrombelastographyThromboplastinAnticoagulantsRecombinant ProteinsThromboplastinbiochemical analytesblood clottingenzymatic activityprothrombin activatorRAPClot™ prototype tubeserumγ-radiation

Identifiers

PMID38927049
PMCPMC11201583

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.