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Heterologous fibrin sealant derived from snake venom: from bench to bedside – an overview

Hemostatic and adhesive agents date back to World War II, when homologous fibrin sealant came onto scene. Considering that infectious diseases can be transmitted via human blood, a new heterologous fibrin sealant was standardized in the 1990s. Its components were a serine protease (a thrombin-like e...

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Detalles Bibliográficos
Autores principales: Ferreira, Rui Seabra, de Barros, Luciana Curtolo, Abbade, Luciana Patrícia Fernandes, Barraviera, Silvia Regina Catharino Sartori, Silvares, Maria Regina Cavariani, de Pontes, Leticia Gomes, dos Santos, Lucilene Delazari, Barraviera, Benedito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379742/
https://www.ncbi.nlm.nih.gov/pubmed/28396682
http://dx.doi.org/10.1186/s40409-017-0109-8
Descripción
Sumario:Hemostatic and adhesive agents date back to World War II, when homologous fibrin sealant came onto scene. Considering that infectious diseases can be transmitted via human blood, a new heterologous fibrin sealant was standardized in the 1990s. Its components were a serine protease (a thrombin-like enzyme) extracted from the venom of Crotalus durissus terrificus snakes and a fibrinogen-rich cryoprecipitate extracted from the blood of Bubalus bubalis buffaloes. This new bioproduct has been used as a coagulant, sealant, adhesive and recently as a candidate scaffold for mesenchymal stem cells and bone and cartilage repair. This review discusses the composition of a new heterologous fibrin sealant, and cites published articles related to its preclinical applications aiming at repairing nervous system traumas and regenerating bone marrow. Finally, we present an innovative safety trial I/II that found the product to be a safe and clinically promising candidate for treating chronic venous ulcers. A multicenter clinical trial, phase II/III, with a larger number of participants will be performed to prove the efficacy of an innovative biopharmaceutical product derived from animal venom. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40409-017-0109-8) contains supplementary material, which is available to authorized users.