Cryopreserved nanostructured fibrin‑agarose hydrogels are efficient and safe hemostatic agents
Metadatos
Mostrar el registro completo del ítemAutor
Casado, Carlos; Cepeda Franco, Carmen; Pereira Arenas, Sheila; Suárez, María Dolores; Gómez Bravo, Miguel Ángel; Alaminos Mingorance, Miguel; Chato Astrain, Jesús; Fernandez-Muñoz, Beatriz; Campos Cuerva, RafaelEditorial
Springer Nature
Materia
Cryopreservation Hemostatic patch Fibrin hydrogel
Fecha
2024-08-21Referencia bibliográfica
Casado, C., Cepeda-Franco, C., Pereira Arenas, S. et al. Cryopreserved nanostructured fibrin-agarose hydrogels are efficient and safe hemostatic agents. Sci Rep 14, 19411 (2024). https://doi.org/10.1038/s41598-024-70456-w
Patrocinador
Instituto de Salud Carlos III through the project “DTS19/00089” (Co-funded by European Regional Development Fund/European Social Fund “A way to make Europe”); Foundation for Innovation and Prospective in Health in Spain (FIPSE) N° Exp. 3728-20; Plan Propio I + D + I of the University of Seville (VIIPPIT-2022-II.4)Resumen
Uncontrolled bleeding during surgery is associated with high mortality and prolonged hospital
stay, necessitating the use of hemostatic agents. Fibrin sealant patches offer an efficient solution
to achieve hemostasis and improve patient outcomes in liver resection surgery. We have previously
demonstrated the efficacy of a nanostructured fibrin-agarose hydrogel (NFAH). However, for the
widespread distribution and commercialization of the product, it is necessary to develop an optimal
preservation method that allows for prolonged stability and facilitates storage and distribution. We
investigated cryopreservation as a potential method for preserving NFAH using trehalose. Structural
changes in cryopreserved NFAH (Cryo-NFAH) were investigated and comparative in vitro and in vivo
efficacy and safety studies were performed with freshly prepared NFAH. We also examined the
long-term safety of Cryo-NFAH versus TachoSil in a rat partial hepatectomy model, including time to
hemostasis, intra-abdominal adhesion, hepatic hematoma, inflammatory factors, histopathological
variables, temperature and body weight, hemocompatibility and cytotoxicity. Structural analyses
demonstrated that Cryo-NFAH retained most of its macro- and microscopic properties after
cryopreservation. Likewise, hemostatic efficacy assays showed no significant differences with fresh
NFAH. Safety evaluations indicated that Cryo-NFAH had a similar overall profile to TachoSil up to
40 days post-surgery in rats. In addition, Cryo-NFAH demonstrated superior hemostatic efficacy
compared with TachoSil while also demonstrating lower levels of erythrolysis and cytotoxicity than
both TachoSil and other commercially available hemostatic agents. These results indicate that Cryo-NFAH is highly effective hemostatic patch with a favorable safety and tolerability profile, supporting
its potential for clinical use.