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A method to measure thrombin activity in a mixture of fibrinogen and thrombin powders

Thrombin and fibrinogen powders are the active components of advanced surgical hemostasis products including the EVARREST Fibrin Sealant Patch. Measuring the enzymatic activity of thrombin in the presence of fibrinogen is challenging, as hydration of the powders in a neutral aqueous environment will...

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Autores principales: DeAnglis, Ashley P., Nur, Israel, Gorman, Anne J., Meidler, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams And Wilkins 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312723/
https://www.ncbi.nlm.nih.gov/pubmed/26991860
http://dx.doi.org/10.1097/MBC.0000000000000560
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author DeAnglis, Ashley P.
Nur, Israel
Gorman, Anne J.
Meidler, Roberto
author_facet DeAnglis, Ashley P.
Nur, Israel
Gorman, Anne J.
Meidler, Roberto
author_sort DeAnglis, Ashley P.
collection PubMed
description Thrombin and fibrinogen powders are the active components of advanced surgical hemostasis products including the EVARREST Fibrin Sealant Patch. Measuring the enzymatic activity of thrombin in the presence of fibrinogen is challenging, as hydration of the powders in a neutral aqueous environment will cause the enzyme to rapidly react with the fibrinogen to form a fibrin clot, which in turn binds and entraps the enzyme thus preventing subsequent measurement of thrombin activity. A novel approach has been developed to overcome this challenge. After isolation of the mixture of powders, an alkaline carbonate solution is used to solubilize the proteins, while reversibly inhibiting the activity of thrombin and preventing clot formation. Once the powders have been fully solubilized, thrombin activity can be restored by neutralization in a buffered fibrinogen solution resulting in fibrin clot formulation. The rate of clot formation can be quantified in a coagulometer to determine the thrombin activity of the original powder. Samples coated with powders containing fibrinogen and varying amounts of thrombin were tested using the method described herein. The results demonstrated that the method could consistently measure the activity of (alpha) thrombin in the presence of fibrinogen over a broad range of thrombin activity levels. The test was successfully validated according to International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use Guidelines and thus is suitable for use as part of a commercial manufacturing process. A method has been developed that enables thrombin activity to be measured in a mixture of fibrinogen and thrombin powders.
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spelling pubmed-53127232017-03-02 A method to measure thrombin activity in a mixture of fibrinogen and thrombin powders DeAnglis, Ashley P. Nur, Israel Gorman, Anne J. Meidler, Roberto Blood Coagul Fibrinolysis Original Articles Thrombin and fibrinogen powders are the active components of advanced surgical hemostasis products including the EVARREST Fibrin Sealant Patch. Measuring the enzymatic activity of thrombin in the presence of fibrinogen is challenging, as hydration of the powders in a neutral aqueous environment will cause the enzyme to rapidly react with the fibrinogen to form a fibrin clot, which in turn binds and entraps the enzyme thus preventing subsequent measurement of thrombin activity. A novel approach has been developed to overcome this challenge. After isolation of the mixture of powders, an alkaline carbonate solution is used to solubilize the proteins, while reversibly inhibiting the activity of thrombin and preventing clot formation. Once the powders have been fully solubilized, thrombin activity can be restored by neutralization in a buffered fibrinogen solution resulting in fibrin clot formulation. The rate of clot formation can be quantified in a coagulometer to determine the thrombin activity of the original powder. Samples coated with powders containing fibrinogen and varying amounts of thrombin were tested using the method described herein. The results demonstrated that the method could consistently measure the activity of (alpha) thrombin in the presence of fibrinogen over a broad range of thrombin activity levels. The test was successfully validated according to International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use Guidelines and thus is suitable for use as part of a commercial manufacturing process. A method has been developed that enables thrombin activity to be measured in a mixture of fibrinogen and thrombin powders. Lippincott Williams And Wilkins 2017-03 2016-04-26 /pmc/articles/PMC5312723/ /pubmed/26991860 http://dx.doi.org/10.1097/MBC.0000000000000560 Text en Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Original Articles
DeAnglis, Ashley P.
Nur, Israel
Gorman, Anne J.
Meidler, Roberto
A method to measure thrombin activity in a mixture of fibrinogen and thrombin powders
title A method to measure thrombin activity in a mixture of fibrinogen and thrombin powders
title_full A method to measure thrombin activity in a mixture of fibrinogen and thrombin powders
title_fullStr A method to measure thrombin activity in a mixture of fibrinogen and thrombin powders
title_full_unstemmed A method to measure thrombin activity in a mixture of fibrinogen and thrombin powders
title_short A method to measure thrombin activity in a mixture of fibrinogen and thrombin powders
title_sort method to measure thrombin activity in a mixture of fibrinogen and thrombin powders
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312723/
https://www.ncbi.nlm.nih.gov/pubmed/26991860
http://dx.doi.org/10.1097/MBC.0000000000000560
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