Bioinspired lipid droplets nanoplatform for periodontitis therapy: Integrated antibacterial, mitochondrial repair, and immunomodulatory functions

Periodontitis, a multifactorial inflammatory disease driven by microbial dysbiosis, dysregulated immunity, and oxidative stress, demands therapeutic strategies that concurrently address interconnected pathological pathways. Here, a biomimetic lipid droplet-based nanoplatform (GA@LDs-CRAMP) is engineered to achieve spatiotemporal coordination of Antibacterial, antioxidant, and immunomodulatory functions for the treatment of periodontitis. Constructed using RAW264.7 macrophage-derived lipid droplets (LDs), the GA@LDs-CRAMP system anchors cathelicidin-related antimicrobial peptide (CRAMP) onto LDs surfaces via lipopolysaccharide (LPS)-stimulated recruitment, while encapsulating gambogic acid (GA) within its hydrophobic core for mitochondria-targeted delivery. The nanoplatform demonstrates comprehensive therapeutic efficacy against periodontitis by suppressing periodontopathogen proliferation, restoring oxidative stress-damaged mitochondria through Reactive Oxygen Species (ROS) scavenging, inhibiting inflammatory cascades via nuclear factor erythroid 2-related factor 2 (Nrf2)/nuclear factor-kappa B (NF-κB)-mediated antioxidant signaling activation, and reprogramming macrophage polarization from pro-inflammatory M1 to tissue-reparative M2 phenotypes. In preclinical periodontitis models, localized delivery of GA@LDs-CRAMP effectively mitigates inflammatory cytokine storms and attenuates alveolar bone resorption. Collectively, this study demonstrates the potential of leveraging lipid droplets organelles to engineer precision-targeted, multifunctional drug delivery systems for periodontitis therapy.

Antimicrobial peptide; Gambogic acid; Lipid droplets; Macrophage polarization; Periodontitis; Targeted mitochondrial therapy.