Preparation of cationic liposomes loaded with Sirtuin 6 plasmid for the treatment of arthritis in rats.

Abstract

Arthritis, ormalizedn by chronic joint inflammation, is increasingly prevalent due to global ageing, placing significant pressure on healthcare systems. Recent studies have identified Sirtuin 6 (Sirt6) as a promising therapeutic target for alleviating arthritis symptoms. This study investigates the therapeutic potential of Sirt6-loaded cationic liposomes in a collagen-induced arthritis (CIA) rat model. Sirt6-loaded cationic liposomes were prepared and ormalizedn using transmission electron microscopy, particle size distribution, polydispersity index (PDI), zeta potential, encapsulation efficiency, in vitro release, and stability studies. The optimal Sirt6 plasmid-to-liposome ratio was established at 1:1000. Characterisation confirmed a spherical morphology, with a particle size of 177.65 ± 2.09 nm, a PDI of 0.216 ± 0.013, and zeta potential of 21.78 ± 1.76 Mv. The liposomes exhibited superior release profiles and storage stability, thus maintaining their integrity for up to 30 days and achieving 90.77 ± 3.35% release efficiency within 24 h. In vitro, the endocytosis of Sirt6-loaded liposomes significantly increased Sirt6 protein expression in chondrocytes (p < 0.01). In vivo, treatment reduced inflammation in liver and spleen tissues and lowered pro-inflammatory cytokines associated with CIA (p < 0.01). These findings support Sirt6-loaded liposomes as a potential novel therapeutic strategy for treatment of arthritis.