Related Experiment Video
Updated: Aug 1, 2025

09:17
Optimizing Extracellular Vesicle Delivery Using a Core-Sheath 3D-Bioprinted Scaffold for Chronic Wound Management
Published on: February 28, 2025
371
Electrosprayed Mesenchymal Stromal Cell Extracellular Matrix Nanoparticles Accelerate Cellular Wound Healing and
Emily N Wandling1, Keera Rhoads1, Dennis E Ohman2,3
1Department of Biomedical Engineering, Virginia Commonwealth University, Richmond, VA 23219, USA.
Pharmaceutics
|April 28, 2023
Summary
New nanoparticles derived from mouse mesenchymal stromal cells (MSCs) show promise for treating acute respiratory distress syndrome (ARDS). These MMSC ECM nanoparticles promote lung healing and combat bacterial infections, offering a potential new therapeutic avenue.
Area of Science:
- Biomedical Engineering
- Regenerative Medicine
- Nanotechnology
Background:
- Acute respiratory distress syndrome (ARDS) lacks effective treatments, with mechanical ventilation posing risks of lung damage and infection.
- The COVID-19 pandemic has highlighted the urgent need for novel ARDS therapies.
- Mesenchymal stromal cells (MSCs) exhibit anti-inflammatory and regenerative properties, making them a potential therapeutic candidate for ARDS.
Purpose of the Study:
- To develop and characterize novel nanoparticles using mouse MSC-derived extracellular matrix (ECM) for ARDS treatment.
- To evaluate the pro-regenerative and antimicrobial potential of these MMSC ECM nanoparticles.
- To assess the biocompatibility and efficacy of MMSC ECM nanoparticles in lung injury models.
Main Methods:
- Characterization of MMSC ECM nanoparticles using size, zeta potential, and mass spectrometry.
- Assessment of nanoparticle biocompatibility with mouse lung epithelial cells and MMSCs.
- Evaluation of MMSC ECM nanoparticles' effect on human lung fibroblast wound healing and inhibition of *Pseudomonas aeruginosa* growth.
Main Results:
- MMSC ECM nanoparticles exhibited an average size of 273.4 nm with a negative zeta potential, facilitating lung tissue penetration.
- Nanoparticles demonstrated biocompatibility with relevant lung cells.
- Significant increase in human lung fibroblast wound healing rate and inhibition of *Pseudomonas aeruginosa* growth were observed.
Conclusions:
- MMSC ECM nanoparticles possess both pro-regenerative and antimicrobial properties beneficial for ARDS.
- These nanoparticles show potential for accelerating lung injury recovery and preventing secondary bacterial infections.
- Further research into MMSC ECM nanoparticles could lead to innovative ARDS treatments.

