Skin and Mucosal Delivery (Focus Group – SMD)
Maria Samara, MEng
PhD student
Stockholm University, Stockholms Lan, Sweden
Chronic wounds, particularly in diabetic patients, represent a major clinical burden due to impaired healing and prolonged inflammation. MicroRNAs regulate multiple stages of tissue repair by coordinating inflammatory and regenerative pathways.1 miR-132 is strongly induced during normal wound healing and promotes fibroblast migration and tissue regeneration, yet is significantly reduced in diabetic wounds.2,3 Nanomedicine-based delivery strategies offer a promising approach to protect and restore therapeutic microRNA signaling locally, enabling pathway-level modulation of chronic wound healing.