“…8 Damaged columnar epithelial cells, persistent inflammatory responses, and severe bacterial infections result in fibroblast transition from the resting state to an active state; the fibroblasts continuously proliferate, migrate, and secrete various extracellular matrix proteins, leading to a high re-obstruction rate of approximately 70-80% after nasolacrimal duct stent implantation. [9][10][11][12][13][14] After a postoperative blockage occurs, another surgery is the only recourse, thus burdening the patients' physical and mental well-being and their financial resources. 7 However, the nasolacrimal ducts in current clinical practice primarily include bare stents composed of silicone, without anti-inflammatory, antibacterial, or anti-fibroblast proliferative properties.…”