A thermosensitive hydrogel achieves sustained co-delivery of two therapeutic agents with distinct properties for preventing aseptic loosening
Abstract
-glycolic acid) triblock copolymers and water. The aqueous system undergoes a sol-to-gel phase transition upon heating with the transition temperature between room temperature and body temperature. Highly hydrophobic Emo is efficiently solubilized into micelles formed by the amphiphilic carrier polymers, while hydrophilic sCT is encapsulated within bovine serum albumin (BSA)-derived nanoparticles to suppress its initial burst release and prolong its release duration from the hydrogel matrix. This dual-delivery platform achieves simultaneous and continuous liberation of both therapeutic agents with distinct properties. In a mouse bone-implanted air pouch model, a single administration of the hydrogel formulation plus the sustained release of active Emo and sCT efficiently suppresses titanium particle-induced aseptic inflammation and osteolysis. Therefore, this local and long-acting co-delivery system holds great promise for preventing wear particle-induced aseptic loosening.
Fields of Study & Subjects
Orthopedic Infections and Treatments
Hydrogels: synthesis
properties
applications
Total Knee Arthroplasty Outcomes
Publication details
- Journal / source
- Biomaterials Science
- Publisher
- Royal Society of Chemistry (RSC)
- Volume
- 14
- Issue
- 8
- Pages
- 2039–2056
- Publication date
- 1 January 2026
- Language
- EN