LusoNano · Technology & research pipeline

Engineering delivery.
Investigating immune response.

A preclinical research framework for functionalized lipid nanocarriers, cell-selective oncology delivery and rational combination therapeutics.

Technology platform

Surface chemistry meets tumor biology.

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.

01 / CARRIER

Nanostructured lipid carriers

Exploration of solid/liquid lipid matrices for small-molecule payloads, with attention to solubility, crystallization, loading and controlled release.

02 / SURFACE

Functionalized interfaces

Investigation of polysarcosine-based surface coatings and ligand-conjugated lipids for selective biological recognition.

03 / TARGET

Cell-specific delivery

Receptor and microenvironment targeting concepts across tumor cells, myeloid populations, stromal fibroblasts and mineralized bone.

Exploratory research pipeline

Programs organized by biological compartment.

The following are research directions and hypotheses, not claims of validated products, completed studies or clinical-stage assets.

Discovery concept
Tumor cells

Tumor-selective pathway modulation

Explore ligand-directed delivery to malignant cells and effects on hypoxia adaptation, inflammatory signaling, resistance pathways and immunotherapy response.

Candidate modalities: functionalized lipid nanoparticles · small-molecule combinations
Discovery concept
Myeloid cells

TAM and myeloid microenvironment modulation

Evaluate selective delivery to immunosuppressive macrophage subsets, including CD206-associated recognition, and assess effects on macrophage survival and T-cell suppression.

Key questions: specificity versus healthy macrophages · receptor engagement · functional selectivity
Discovery concept
Fibroblasts

CAF phenotype and immune exclusion

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.

Readouts: active TGF-β · ECM architecture · CAF phenotypes · CD8+ infiltration
Discovery concept
Bone niche

Bone-localized oncology delivery

Explore mineral-affinity ligands as a means of enriching drug carriers at bone surfaces, with special attention to release into adjacent metastatic marrow tissue.

Key questions: bone versus lesion localization · local exposure · systemic off-target distribution
Research framework
Combinations

Nanomedicine-enabled immunotherapy combinations

Study whether selective pathway modulation can complement checkpoint blockade or cellular immunotherapy while preserving beneficial immune-cell function.

Evidence strategy: single-agent controls · combination comparisons · toxicity and immune-function endpoints
Preclinical validation

Mechanism before claims.

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.

FormulationParticle size, dispersity, lipid compatibility, loading and release
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TargetingReceptor-dependent uptake and off-target comparison
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Biological activityTarget engagement, phenotype and T-cell function
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TranslationExposure, safety, manufacturability and model limitations

Research concepts only. No human therapeutic claims, investigational products for sale, or clinical services are represented on this page.

Research environment

Precision science, from concept to preclinical evaluation.

Illustrative imagery; not photographs of LusoNano facilities or personnel.