Rational design of FAP-targeted sEVs delivered by microneedles for precision treatment of hypertrophic scars via ferroptosis in hypertrophic scar fibroblasts
Abstract
rescue experiments using the ferroptosis inhibitor Ferrostatin-1 confirmed that these effects were specifically mediated by ferroptosis. Collectively, these results support FAP as an actionable targeting handle for preferential delivery to scar fibroblasts and suggest that ferroptosis-associated inactivation of HSFs can be leveraged through a microneedle-enabled, locally retained sEV formulation.
Fields of Study & Subjects
Proteoglycans and glycosaminoglycans research
Advancements in Transdermal Drug Delivery
Extracellular vesicles in disease
Publication details
- Journal / source
- Materials Today Bio
- Volume
- 38
- Pages
- 103117–103117
- Publication date
- 13 April 2026
- Language
- EN