Literature DB >> 16673270

Comparison of recombinant human thrombin and plasma-derived human alpha-thrombin.

Paul D Bishop1, Kenneth B Lewis, Jody Schultz, Kathleen M Walker.   

Abstract

Bleeding can be a serious complication of surgery, and topical thrombin is widely used as an adjunct to hemostasis in diverse surgical settings. The potent hemostatic properties of thrombin derive from its ability to activate platelets directly to aggregate and adhere to damaged vessels and to catalyze the formation simultaneously of a fibrin matrix. Application of exogenous thrombin bypasses the physiological process of generating a thrombin burst by directly initiating the terminal reactions of blood clot formation. Currently, thrombin used to control surgical bleeding is primarily from bovine plasma, with a small percentage from human plasma. Human thrombin isolated from pooled plasma carries the risk of transmitting plasma-borne pathogens or prion diseases. The bovine preparations have been associated with protein and preparative contaminants that pose potential risks of developing cross-reacting antibodies. There is a need for a pure therapeutic preparation of human thrombin. Recombinant human thrombin (rhThrombin) has been efficiently produced from a prethrombin-1 precursor obtained from Chinese hamster ovary cell culture. This rhThrombin is substantially free of process-derived contaminants and has been characterized extensively in terms of composition, primary, secondary, and tertiary structure, enzymatic activity; and in vivo pharmacology. In vivo studies of topically applied rhThrombin have shown it is effective in achieving hemostasis in a rabbit liver excisional wound model. Clinical studies are ongoing to evaluate the safety and efficacy of rhThrombin as an adjunct to hemostasis in patients undergoing surgery.

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Year:  2006        PMID: 16673270     DOI: 10.1055/s-2006-939558

Source DB:  PubMed          Journal:  Semin Thromb Hemost        ISSN: 0094-6176            Impact factor:   4.180


  7 in total

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Journal:  Appl Microbiol Biotechnol       Date:  2022-10-05       Impact factor: 5.560

2.  Managing gastric varices.

Authors:  Deema Sallout; Eric Tatro; Douglas G Adler
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Review 3.  An overview of enzymatic reagents for the removal of affinity tags.

Authors:  David S Waugh
Journal:  Protein Expr Purif       Date:  2011-08-19       Impact factor: 1.650

4.  Thrombin a-chain: activation remnant or allosteric effector?

Authors:  Isis S R Carter; Amanda L Vanden Hoek; Edward L G Pryzdial; Ross T A Macgillivray
Journal:  Thrombosis       Date:  2010-12-09

5.  Characterization of thrombin derived from human recombinant prothrombin.

Authors:  Ann Lövgren; Johanna Deinum; Steffen Rosén; Pia Bryngelhed; Per Rosén; Kenny M Hansson
Journal:  Blood Coagul Fibrinolysis       Date:  2015-07       Impact factor: 1.276

6.  Activated Serum Increases In Vitro Cellular Proliferation and Growth Factor Expression of Musculoskeletal Cells.

Authors:  Owen P Karsmarski; Benjamin C Hawthorne; Antonio Cusano; Matthew R LeVasseur; Ian J Wellington; Mary Beth McCarthy; Mark P Cote; Augustus D Mazzocca
Journal:  J Clin Med       Date:  2022-06-15       Impact factor: 4.964

7.  Topical recombinant thrombin at a concentration of 1000 IU/mL reliably shortens in vivo TTH and delivers durable hemostasis in the presence of heparin anticoagulation and clopidogrel platelet inhibition in a rabbit model of vascular bleeding.

Authors:  Steven D Hughes; Paul D Bishop; Richard Garcia; Tracy Zhang; W Allan Alexander
Journal:  Ann Surg Innov Res       Date:  2009-11-19
  7 in total

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