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February 2, 2026Bioengineering1 citationsOpen Access

Chronic In Vivo Biostability and Biocompatibility Evaluation of Polyether-Urethane-Based Balloon Implants for Cardiac Application in a Porcine Model

MKMin-Gi KimPusan National UniversityJSJae-Young SeoPusan National UniversityJKJune H. KimCity University of New York

Key Result

A polyether-urethane-based balloon implant deployed in 7 pigs demonstrated structural stability and biocompatibility over 24 weeks, with no evidence of degradation or significant inflammation.

Key Points

  • The aim is to evaluate the long-term biostability and biocompatibility of polyurethane-based implants in dynamic cardiac environments.
  • Evaluated balloon-shaped implants in seven pigs over 24 weeks.
  • Conducted material characterization using SEM, GPC, FT-IR, and 1H-NMR.
  • Performed histological analysis for tissue response and thrombosis.
  • Assessed biocompatibility via ISO 10993 standards.
  • Preserved surface morphology and chemical bonds observed via SEM and FT-IR.
  • Stable molecular weight indicated by GPC with no signs of degradation.
  • Minimal thrombosis and inflammatory response noted in histological evaluations.
  • Biocompatibility confirmed with no toxicologically significant findings under ISO standards.

Structured PICO

Does a polyether-urethane-based balloon implant demonstrate long-term biostability and biocompatibility when deployed adjacent to the tricuspid valve annulus in a porcine model?

P
Population
7 pigs implanted with a polyether-urethane-based balloon device adjacent to the tricuspid valve annulus, followed for 24 weeks.
I
Intervention
Polyether-based polyurethane balloon-shaped implant (designed as a three-dimensional intracardiac spacer), deployed via percutaneous femoral vein access and positioned adjacent to the tricuspid valve annulus for 24 weeks
O
Outcome
Biostability and biological safety evaluated through material characterization (SEM, GPC, FT-IR, and 1H-NMR) and histological analysis at 24 weekssafety

Polyether-urethane-based balloon implants demonstrate long-term biostability and biological safety in a dynamic porcine cardiac environment, supporting their potential use in catheter-delivered structural heart interventions.

Abstract

Polyurethane-based implantable devices (PUIDs) delivered via catheter are increasingly used in structural heart interventions; however, limited in vivo data exist regarding their long-term biostability and biological safety. This study evaluated a balloon-shaped implant made of Pellethane®, a polyether-based polyurethane, designed as a three-dimensional intracardiac spacer and deployed via percutaneous femoral vein access. The device was chronically positioned adjacent to the tricuspid valve annulus in seven pigs for 24 weeks. Explanted devices and surrounding tissues were evaluated through material characterization (SEM, GPC, FT-IR, and 1H-NMR) and histological analysis. SEM and FT-IR confirmed preserved surface morphology and chemical bonds, GPC showed stable molecular weight, and 1H-NMR revealed intact urethane and ether linkages. Materials characterization revealed no evidence of hydrolytic or oxidative degradation, indicating structural stability of the devices. Histological analysis showed stable device positioning with minimal thrombosis or inflammatory response. Biocompatibility was confirmed via ISO 10993-1:2018 Standard (International Organization for Standardization (ISO): Geneva, Switzerland, 2018), and extractable substances were evaluated under exhaustive extraction conditions specified by ISO 10993-18:2020 (International Organization for Standardization (ISO): Geneva, Switzerland, 2020), with no toxicologically significant findings. These findings support the long-term biostability and biological safety of the PUIDs in dynamic cardiac environments, informing future design criteria for catheter-delivered cardiovascular devices.

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Cite This Study

Kim et al. (2026) studied this question. Polyether-urethane-based balloon implant (Pellethane®) was evaluated on Long-term biostability and biological safety. A polyether-urethane-based balloon implant deployed in 7 pigs demonstrated structural stability and biocompatibility over 24 weeks, with no evidence of degradation or significant inflammation.

synapsesocial.com/papers/6980fc37c1c9540dea80df60https://doi.org/10.3390/bioengineering13020168
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