Preclinical in vitro and in vivo results of the new silk vista flow diverter with P8RI coating.

Aneurysm Flow Diverter Platelets

Journal

Journal of neurointerventional surgery
ISSN: 1759-8486
Titre abrégé: J Neurointerv Surg
Pays: England
ID NLM: 101517079

Informations de publication

Date de publication:
24 Jun 2024
Historique:
received: 08 03 2024
accepted: 07 06 2024
medline: 25 6 2024
pubmed: 25 6 2024
entrez: 24 6 2024
Statut: aheadofprint

Résumé

Flow diverting stents (FDS) have transformed the treatment of intracranial aneurysms; however, their metallic structure associated with their intra-luminal positioning hamper angiographic and clinical outcomes. Therefore, there is a need to develop FDS with optimized surfaces that reduce thrombogenicity while promoting the healing process and endothelialization. P8RI, a peptide mimicking the CD31 protein, was previously developed and grafted onto Silk Vista (SV) FDS. P8RI-SV and bare-SV were used in vitro in a blood loop model to test their hemocompatibility using human whole blood and in vivo using the rabbit elastase model for optical coherence tomography (OCT) comparisons of neointimal formation at day 5 and day 28. After blood loop incubation, P8RI-SV showed significant reduction in fibrin binding (p=0.004) and platelet adhesion (p=0.041) compared with bare-SV. Similarly, derivative markers measured in blood, thromboxane B2 (platelet activation) and Thrombin-Antithrombin III complexes (coagulation activation), were also significantly reduced in the P8RI-SV group (both p=0.002). In vivo, complete or near-complete occlusion was reached in all aneurysms (n=6) at day 28. Excellent rate of stent-coverage ratio was obtained at day 5 (89.3% (79.1%-98.7%)) comparable to the observation at day 28 (91.8% (79.1%-100%); p=0.44). These rates were significantly higher compared with bare-SV at day 5 (77.8% (58.3%-86.8%); p<0.001) and at day 28 (67.7% (52.6%-88.9%); p<0.0001). In vitro results confirm enhanced hemocompatibility with a significant anti-thrombotic effect of the P8RI-SV. In vivo results provide evidence of rapid neo-intimal growth reaching near-complete tissue healing as early as day 5 in a rabbit model.

Sections du résumé

BACKGROUND BACKGROUND
Flow diverting stents (FDS) have transformed the treatment of intracranial aneurysms; however, their metallic structure associated with their intra-luminal positioning hamper angiographic and clinical outcomes. Therefore, there is a need to develop FDS with optimized surfaces that reduce thrombogenicity while promoting the healing process and endothelialization.
METHODS METHODS
P8RI, a peptide mimicking the CD31 protein, was previously developed and grafted onto Silk Vista (SV) FDS. P8RI-SV and bare-SV were used in vitro in a blood loop model to test their hemocompatibility using human whole blood and in vivo using the rabbit elastase model for optical coherence tomography (OCT) comparisons of neointimal formation at day 5 and day 28.
RESULTS RESULTS
After blood loop incubation, P8RI-SV showed significant reduction in fibrin binding (p=0.004) and platelet adhesion (p=0.041) compared with bare-SV. Similarly, derivative markers measured in blood, thromboxane B2 (platelet activation) and Thrombin-Antithrombin III complexes (coagulation activation), were also significantly reduced in the P8RI-SV group (both p=0.002). In vivo, complete or near-complete occlusion was reached in all aneurysms (n=6) at day 28. Excellent rate of stent-coverage ratio was obtained at day 5 (89.3% (79.1%-98.7%)) comparable to the observation at day 28 (91.8% (79.1%-100%); p=0.44). These rates were significantly higher compared with bare-SV at day 5 (77.8% (58.3%-86.8%); p<0.001) and at day 28 (67.7% (52.6%-88.9%); p<0.0001).
CONCLUSION CONCLUSIONS
In vitro results confirm enhanced hemocompatibility with a significant anti-thrombotic effect of the P8RI-SV. In vivo results provide evidence of rapid neo-intimal growth reaching near-complete tissue healing as early as day 5 in a rabbit model.

Identifiants

pubmed: 38914459
pii: jnis-2024-021694
doi: 10.1136/jnis-2024-021694
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: JC received an educational grant from Medtronic, Phenox and Microvention; and received honoraria for lectures from Balt. LS is a consultant for Microvention, Balt, Phenox, Stryker, Medtronic. AR received honoraria for lectures from Balt. CM received honoraria for lectures from Balt.

Auteurs

Jonathan Cortese (J)

NEURI -Brain vascular center- Interventional Neuroradiology, Bicetre University-Hospital, Le Kremlin-Bicetre, France jonathan.cortese@aphp.fr.
INSERM U1195, Paris-Saclay University, Le Kremlin-Bicêtre, France.
XLIM UMR CNRS, University of Limoges, Limoges, France.

Géraud Forestier (G)

XLIM UMR CNRS, University of Limoges, Limoges, France.
Neuroradiology department, University Hospital of Limoges, Limoges, Limousin, France.

Sylvia M Bardet (SM)

XLIM UMR CNRS, University of Limoges, Limoges, France.
UMR CNRS no 7252, XLIM, Limoges, Aquitaine, France.

Marie-Laure Perrin (ML)

XLIM UMR CNRS, University of Limoges, Limoges, France.

Maxime Baudouin (M)

XLIM UMR CNRS, University of Limoges, Limoges, France.
Neuroradiology department, University Hospital of Limoges, Limoges, Limousin, France.

Alexis Belgacem (A)

XLIM UMR CNRS, University of Limoges, Limoges, France.

Romain Chauvet (R)

XLIM UMR CNRS, University of Limoges, Limoges, France.
Vascular Surgery, Limoges University-Hospital, Limoges, Nouvelle-Aquitaine, France.

Voahirana Ratsimbazafy (V)

Pharmacy department, Limoges University-Hospital, Limoges, France.
IFR 145 GEIST, Institut d'Epidemiologie Neurologique et de Neurologie Tropicale, INSERM, UMR, University of Limoges, Limoges, France.

Gregory Sasselina (G)

XLIM UMR CNRS, University of Limoges, Limoges, France.

Daphnée Chandellier (D)

XLIM UMR CNRS, University of Limoges, Limoges, France.

Jérémy Mounier (J)

XLIM UMR CNRS, University of Limoges, Limoges, France.

Claude Couquet (C)

XLIM UMR CNRS, University of Limoges, Limoges, France.

Florence Bosselut (F)

XLIM UMR CNRS, University of Limoges, Limoges, France.

Laurent Spelle (L)

NEURI -Brain vascular center- Interventional Neuroradiology, Bicetre University-Hospital, Le Kremlin-Bicetre, France.
INSERM U1195, Paris-Saclay University, Le Kremlin-Bicêtre, France.

Charbel Mounayer (C)

XLIM UMR CNRS, University of Limoges, Limoges, France.
Neuroradiology department, University Hospital of Limoges, Limoges, Limousin, France.

Faraj Terro (F)

XLIM UMR CNRS, University of Limoges, Limoges, France.
Cell Biology, Limoges University, Limoges, Nouvelle-Aquitaine, France.

Aymeric Rouchaud (A)

XLIM UMR CNRS, University of Limoges, Limoges, France.
Neuroradiology department, University Hospital of Limoges, Limoges, Limousin, France.

Classifications MeSH