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Multi-Scale Modification of Metallic Implants With Pore Gradients, Polyelectrolytes and Their Indirect Monitoring In vivo
Published on: July 1, 2013
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A multi-targeting bionanomatrix coating to reduce capsular contracture development on silicone implants.
Patrick Hwang1,2, Chung Min Shin3, Jennifer A Sherwood1
1Endomimetics, LLC, Birmingham, AL, 35242, USA.
Biomaterials Research
|April 22, 2023
Summary
A novel nitric oxide (NO)-releasing bionanomatrix coating effectively reduces capsular contracture around silicone implants. This innovative coating targets fibrosis and inflammation, promoting improved healing and reducing implant complications.
Area of Science:
- Biomaterials Science
- Regenerative Medicine
- Medical Device Coatings
Background:
- Capsular contracture is a major complication of silicone implants, driven by excessive foreign body responses and fibrotic tissue formation.
- Key mechanisms include myofibroblast differentiation via the transforming growth factor beta (TGF-β)/p-SMADs pathway and biofilm-induced chronic inflammation.
- Current treatments lack multi-targeted approaches for capsular contracture development.
Purpose of the Study:
- To develop and evaluate a multi-targeting nitric oxide (NO)-releasing bionanomatrix coating for silicone implants.
- The coating aims to mitigate capsular contracture by addressing myofibroblast differentiation, inflammation, and infection.
- To assess the efficacy of the bionanomatrix coating in reducing capsular contracture in a preclinical mouse model.
Main Methods:
- Characterization of the bionanomatrix coating using rheology, SEM, nanoindentation, and NO release kinetics.
- In vitro evaluation of monocyte adhesion and Staphylococcus epidermidis biofilm formation on coated silicone implants.
- Subcutaneous implantation in a mouse model to assess capsular contracture, fibrosis, capsule thickness, and inflammatory markers (TGF-β/SMADs, cytokines).
Main Results:
- The bionanomatrix coating demonstrated mechanical stability, sustained NO release for over a month, and reduced monocyte adhesion and biofilm formation in vitro.
- In vivo studies showed a significant reduction in capsule thickness around bionanomatrix-coated implants.
- Inhibition of TGF-β/p-SMADs signaling led to decreased myofibroblast differentiation and extracellular matrix production, with a shift from M1 to M2 macrophage markers indicating reduced inflammation and promoted healing.
Conclusions:
- The NO-releasing bionanomatrix coating effectively reduces capsular contracture and promotes healing on silicone implants.
- The coating's multi-targeting mechanism inhibits myofibroblast differentiation, fibrotic tissue formation, and inflammation.
- This innovative coating offers a promising strategy to improve outcomes for silicone implant procedures.

