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Loboda, O.

Publications and source records attributed to Loboda, O..

2 recordsLinked to original sources

A Bioelectronic Scaffold for Label-Free, Real-Time Monitoring of Wound Healing

Chronic wounds and severe burns pose a major clinical challenge, as they often heal slowly or fail to respond to conventional treatments. In addition, there is a critical lack of tools for personalized, continuous monitoring of the healing process. Although progress has been made in both regenerative biomaterials and wearable biosensors, their integration into a unified platform that enables in situ, real-time monitoring of wound healing remains a major challenge. Here, we present a multifunctional bioelectronic scaffold that combines regenerative capability with real-time sensing of cellular activity. The scaffold was fabricated by electrospinning polycaprolactone (PCL) functionalized with the bioactive, self-assembling peptide fluorenylmethoxycarbonyl-phenylalanine-arginine-glycine-aspartic acid (Fmoc-FRGD) to promote cell adhesion and proliferation. For electrical sensing, biocompatible MXene (Ti3C2TX) electrodes were conformally deposited onto the nanofibrous matrix, preserving its biological functionality. This system enables label-free, real-time monitoring of cell viability and coverage using electrical impedance spectroscopy (EIS), offering continuous and quantitative insight into cellular adhesion and proliferation. Extracted impedance parameters at low frequencies exhibit a strong correlation with both cell viability and coverage, providing a non-destructive indicator of wound closure and healing dynamics. This platform offers a promising strategy for advanced wound care, integrating real-time monitoring with biologically supportive materials.

bioengineering↗

Stable, Easy-to-Handle, Fully Autologous Electrospun Polymer-Peptide Skin Equivalent for Severe Burn Injuries

Severe burn injuries represent a significant clinical challenge due to their complex healing process and the high risk of complications, including infection, scarring, and contracture formation. Current therapeutic approaches for burn wound treatment include autologous donor-site grafting and advanced cell therapy techniques like cultured epidermal autografts (CEA), which successfully facilitate wound closure through re-epithelialization. However, CEAs are limited by fragility, shrinkage, lack of a dermal layer, and risks of contamination. Here, aiming to overcome these limitations, we developed a personalized skin equivalent featuring an engineered scaffold composed of electrospun polycaprolactone (PCL) functionalized with the bioactive peptide fluorenylmethyloxycarbonyl-phenylalanine-arginine-glycine-aspartic acid (Fmoc-FRGD). This scaffold is designed to mimic the natural extracellular matrix (ECM), promoting cellular adhesion, integration, and proliferation while maintaining structural integrity. In-vitro analysis demonstrated the scaffolds ability to support multi-layered human skin cell growth, while in-vivo experiments confirmed its efficacy in facilitating wound closure and full-thickness skin regeneration in a murine model. This bioengineered skin equivalent is mechanically robust, easy to handle, fully autologous and exhibits no contraction, offering a transformative therapeutic alternative for the treatment of severe burn injuries.

bioengineering↗