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Antithrombotic and Antimicrobial Potential of S-Nitroso-1-Adamantanethiol-Impregnated Extracorporeal Circuit.
Lautner-Csorba, Orsolya; Gorur, Roopa; Major, Terry; Wu, Jianfeng; Sheet, Partha; Hill, Joseph; Yu, Minzhi; Xi, Chuanwu; Bartlett, Robert H; Schwendeman, Steven P; Lautner, Gergely; Meyerhoff, Mark E.
Afiliação
  • Lautner-Csorba O; From the Department of Surgery, University of Michigan, Ann Arbor, Michigan.
  • Gorur R; Department of Chemistry, University of Michigan, Ann Arbor, Michigan.
  • Major T; From the Department of Surgery, University of Michigan, Ann Arbor, Michigan.
  • Wu J; Department of Environmental Health Sciences, University of Michigan, Ann Arbor, Michigan.
  • Sheet P; Department of Pharmaceutical Sciences, University of Michigan, Ann Arbor, Michigan.
  • Hill J; From the Department of Surgery, University of Michigan, Ann Arbor, Michigan.
  • Yu M; Department of Pharmaceutical Sciences, University of Michigan, Ann Arbor, Michigan.
  • Xi C; Department of Environmental Health Sciences, University of Michigan, Ann Arbor, Michigan.
  • Bartlett RH; From the Department of Surgery, University of Michigan, Ann Arbor, Michigan.
  • Schwendeman SP; Department of Pharmaceutical Sciences, University of Michigan, Ann Arbor, Michigan.
  • Lautner G; Department of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan.
  • Meyerhoff ME; Department of Pharmaceutical Sciences, University of Michigan, Ann Arbor, Michigan.
ASAIO J ; 2024 Jul 22.
Article em En | MEDLINE | ID: mdl-39037705
ABSTRACT
This study presents the utilization of a novel, highly lipophilic nitric oxide (NO) donor molecule, S-nitroso-1-adamantanethiol (SNAT), for developing an NO-emitting polymer surface aimed at preventing thrombus formation and bacterial infection in extracorporeal circuits (ECCs). S-nitroso-1-adamantanethiol, a tertiary nitrosothiol-bearing adamantane species, was synthesized, characterized, and used to impregnate polyvinyl chloride (PVC) tubing for subsequent in vivo evaluation. The impregnation process with SNAT preserved the original mechanical strength of the PVC. In vitro assessments revealed sustained NO release from the SNAT-impregnated PVC tubing (iSNAT), surpassing or matching endothelial NO release levels for up to 42 days. The initial NO release remained stable even after 1 year of storage at -20°C. The compatibility of iSNAT with various sterilization techniques (OPA Plus, hydrogen peroxide, EtO) was tested. Acute in vivo experiments in a rabbit model demonstrated significantly reduced thrombus formation in iSNAT ECCs compared with controls, indicating the feasibility of iSNAT to mitigate coagulation system activation and potentially eliminate the need for systemic anticoagulation. Moreover, iSNAT showed substantial inhibition of microbial biofilm formation, highlighting its dual functionality. These findings underscore the promising utility of iSNAT for long-term ECC applications, offering a multifaceted approach to enhancing biocompatibility and minimizing complications.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ASAIO J / ASAIO journal / ASAIO. j Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ASAIO J / ASAIO journal / ASAIO. j Ano de publicação: 2024 Tipo de documento: Article