Accelerated Wound Healing Sustained Release Nanoparticles

University of Pittsburgh researchers have developed a sustained-release wound healing therapy that can deliver TGF-β3 (Transforming Growth Factor) via nanoparticles at surgical sites, aiming to promote regenerative tissue repair, enhance tensile strength, and reduce post-operative scarring in soft tissues.

Description

Surgical wound healing in soft tissues (e.g. fascia or cartilage) is often compromised by fibrosis and inadequate regeneration. Adult wounds predominantly heal with TGF-β1/β2-driven fibrosis, leading to scar formation that weakens the repaired tissue. Examples include abdominal trauma, such as incisional hernias, which remains a serious complication due to insufficient healing strength and can lead to poorer outcomes for patients. Cartilage injuries also heal poorly, as cartilage has limited intrinsic regenerative capacity. There is an unmet need for therapies that enhance tissue regeneration and strength while minimizing scar tissue. Notably, TGF-β3 has been shown to attenuate collagen scarring and improve wound quality. Direct use of TGF-β3 is limited by its short half-life and instability (sensitive to temperature and pH), necessitating repeated dosing, which is costly, time consuming, and inefficient. A method to sustainably deliver TGF-β3 locally at the wound site could greatly improve healing outcomes.

Applications

- Post-operative wound repair
- Hernia Treatment
- Diabetic wound healing

Advantages

TGF-β3 delivery using biodegradable sustained-release nanoparticles, creates a localized reservoir of the regenerative growth factor. This approach maintains therapeutic TGF-β3 levels at the wound for several weeks, avoiding the burst-release and rapid clearance observed with standard gels or injections. By outperforming existing closure techniques and biologics, this platform can potentially reduce complications like wound dehiscence, anastomotic leakage, and excessive scarring. It requires only a single application at surgery, and the nanoparticle system releases TGF-β3 to guide the healing process.

Invention Readiness

The TGF-β3-loaded nanoparticles with a combination of matrices have been prototyped and tested in preclinical models. In tissue studies, a single application of TGF-β3 nanoparticles significantly increased wound tensile strength compared to blank nanoparticles and soluble TGF-β3 dose control. The sustained-release formulation has demonstrated stable TGF-β3 release over multiple weeks in vitro. Ongoing development includes optimizing dosage and nanoparticle configurations. Readiness level: preclinical proof-of-concept with in vitro and tissue testing data.

IP Status

Patent Pending