Preclinical and clinical evaluation of a novel synthetic bioresorbable, on-demand, light-activated sealant in vascular reconstruction.


Journal

The Journal of cardiovascular surgery
ISSN: 1827-191X
Titre abrégé: J Cardiovasc Surg (Torino)
Pays: Italy
ID NLM: 0066127

Informations de publication

Date de publication:
Oct 2019
Historique:
pubmed: 16 5 2019
medline: 18 12 2019
entrez: 16 5 2019
Statut: ppublish

Résumé

Synthetic vascular material use, particularly polytetrafluoroethylene- (PTFE) -based, can be associated with bleeding, which may increase operative time and blood loss. None of the commercially available sealants designed to ensure hemostasis combine bioresorption, high viscosity, hydrophobicity, and compliance with the underlying tissue and on-demand activation. A study was designed to assess the biocompatibility and in-vivo performance and bioresorption of a new synthetic on-demand light-activated poly(glycerol-sebacate) acrylate- (PGSA) -based SETALIUM™ Vascular Sealant (TISSIUM, Paris, France) in three large animal studies of open vascular carotid and aortic surgery. The pre-clinical results were then translated into a clinical setting in a prospective, single-arm multicenter study in patients requiring carotid endarterectomy using an ePTFE patch. The biocompatibility testing showed that the PGSA-based SETALIUM™ Vascular Sealant did not induce any significant toxic reaction at a standard clinical dose nor at doses up to 40 times the equivalent intended clinical dose. The PGSA-based sealant was shown to be non-pyrogenic, non-sensitizing, non-irritant, non-clastogenic, and non-mutagenic. The animal studies showed excellent performance and safety results, with clinically significant hemostasis achieved in 100% of the animals in both carotid and aorta studies and excellent local tolerance. Histopathology and morphometric analyses showed surface-based gradual and sustained bioresorption of the PGSA-based sealant up to 86% at 12 months. In the clinical study, the application of the PGSA-based sealant resulted in good performance and safety, with immediate hemostasis achieved in 84% of the cases and no adverse event related to the sealant reported through the one-year follow-up. The new synthetic on-demand light activated PGSA-based SETALIUM™ Vascular Sealant investigated in our studies demonstrated good biocompatibility, sustained and gradual surface based bioresorption, and acceptable safety profile in animal studies. In addition, the first in-human use showed that the sealant is a safe and effective alternative to achieve fast and controlled hemostasis in vascular carotid reconstructions. A larger randomized controlled study will allow further validation of these encouraging preliminary results.

Sections du résumé

BACKGROUND BACKGROUND
Synthetic vascular material use, particularly polytetrafluoroethylene- (PTFE) -based, can be associated with bleeding, which may increase operative time and blood loss. None of the commercially available sealants designed to ensure hemostasis combine bioresorption, high viscosity, hydrophobicity, and compliance with the underlying tissue and on-demand activation.
METHODS METHODS
A study was designed to assess the biocompatibility and in-vivo performance and bioresorption of a new synthetic on-demand light-activated poly(glycerol-sebacate) acrylate- (PGSA) -based SETALIUM™ Vascular Sealant (TISSIUM, Paris, France) in three large animal studies of open vascular carotid and aortic surgery. The pre-clinical results were then translated into a clinical setting in a prospective, single-arm multicenter study in patients requiring carotid endarterectomy using an ePTFE patch.
RESULTS RESULTS
The biocompatibility testing showed that the PGSA-based SETALIUM™ Vascular Sealant did not induce any significant toxic reaction at a standard clinical dose nor at doses up to 40 times the equivalent intended clinical dose. The PGSA-based sealant was shown to be non-pyrogenic, non-sensitizing, non-irritant, non-clastogenic, and non-mutagenic. The animal studies showed excellent performance and safety results, with clinically significant hemostasis achieved in 100% of the animals in both carotid and aorta studies and excellent local tolerance. Histopathology and morphometric analyses showed surface-based gradual and sustained bioresorption of the PGSA-based sealant up to 86% at 12 months. In the clinical study, the application of the PGSA-based sealant resulted in good performance and safety, with immediate hemostasis achieved in 84% of the cases and no adverse event related to the sealant reported through the one-year follow-up.
CONCLUSIONS CONCLUSIONS
The new synthetic on-demand light activated PGSA-based SETALIUM™ Vascular Sealant investigated in our studies demonstrated good biocompatibility, sustained and gradual surface based bioresorption, and acceptable safety profile in animal studies. In addition, the first in-human use showed that the sealant is a safe and effective alternative to achieve fast and controlled hemostasis in vascular carotid reconstructions. A larger randomized controlled study will allow further validation of these encouraging preliminary results.

Identifiants

pubmed: 31089086
pii: S0021-9509.19.10783-5
doi: 10.23736/S0021-9509.19.10783-5
doi:

Substances chimiques

Acrylates 0
Decanoates 0
Polymers 0
Tissue Adhesives 0
poly(glycerol-sebacate) 0
Glycerol PDC6A3C0OX

Types de publication

Clinical Trial Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

599-611

Auteurs

Quentin Pellenc (Q)

Department of Vascular and Thoracic Surgery, Bichat University Hospital, AP-HP, Paris, France - quentin.pellenc@aphp.fr.
Paris-Diderot Paris VII University, Paris, France - quentin.pellenc@aphp.fr.

Joseph Touma (J)

Department of Vascular Surgery, Henri Mondor University Hospital, AP-HP, Créteil, France.

Raphael Coscas (R)

Department of Vascular Surgery, Ambroise Paré University Hospital, AP-HP, Boulogne-Billancourt, France.
Inserm U1018, Epidemiology and Population Health Research Center (CESP), Versailles Saint-Quentin-en-Yvelines University, Federal University of Paris-Saclay, Villejuif, France.

Grégoire Edorh (G)

TISSIUM Biomorphic Programmable Polymers, Paris, France.

Maria Pereira (M)

TISSIUM Biomorphic Programmable Polymers, Paris, France.

Jeffrey Karp (J)

Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Yves Castier (Y)

Department of Vascular and Thoracic Surgery, Bichat University Hospital, AP-HP, Paris, France.
Paris-Diderot Paris VII University, Paris, France.

Pascal Desgranges (P)

Department of Vascular Surgery, Henri Mondor University Hospital, AP-HP, Créteil, France.

Jean Marc Alsac (JM)

Department of Vascular Surgery, Georges Pompidou European University Hospital, AP-HP, Paris, France.
Paris-Descartes Paris V University, Paris, France.
Inserm UMR 970, Paris Cardiovascular Research Center (PARCC), Paris, France.

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Classifications MeSH