Nanostructured lipid carriers
Exploration of solid/liquid lipid matrices for small-molecule payloads, with attention to solubility, crystallization, loading and controlled release.
A preclinical research framework for functionalized lipid nanocarriers, cell-selective oncology delivery and rational combination therapeutics.
Our research concepts examine how lipid matrix composition, stealth coatings, and receptor-directed surface ligands may influence payload retention, biodistribution and cellular exposure. Specific performance characteristics remain to be established experimentally.
Exploration of solid/liquid lipid matrices for small-molecule payloads, with attention to solubility, crystallization, loading and controlled release.
Investigation of polysarcosine-based surface coatings and ligand-conjugated lipids for selective biological recognition.
Receptor and microenvironment targeting concepts across tumor cells, myeloid populations, stromal fibroblasts and mineralized bone.
The following are research directions and hypotheses, not claims of validated products, completed studies or clinical-stage assets.
Explore ligand-directed delivery to malignant cells and effects on hypoxia adaptation, inflammatory signaling, resistance pathways and immunotherapy response.
Evaluate selective delivery to immunosuppressive macrophage subsets, including CD206-associated recognition, and assess effects on macrophage survival and T-cell suppression.
Investigate FAP-associated delivery and complementary modulation of TGF-β signaling, oxidative pathways and fibroblast differentiation to assess whether immune-excluding stroma can be normalized.
Explore mineral-affinity ligands as a means of enriching drug carriers at bone surfaces, with special attention to release into adjacent metastatic marrow tissue.
Study whether selective pathway modulation can complement checkpoint blockade or cellular immunotherapy while preserving beneficial immune-cell function.
Each research concept calls for analytical characterization and biologically relevant comparison against free drug and nonfunctionalized carriers.
Priority measurements include drug loading and stability, receptor specificity, cellular uptake versus intracellular drug exposure, tissue distribution, target engagement and immune functional outcomes.
Research concepts only. No human therapeutic claims, investigational products for sale, or clinical services are represented on this page.
Illustrative imagery; not photographs of LusoNano facilities or personnel.