In 2025, Science Advances published a groundbreaking study revealing that PEGylated liposomes modified with RGD peptides significantly enhanced penetration and cellular uptake in tumor tissues. This system leverages pH-responsive mechanisms to enable highly precise, controlled drug release within the acidic tumor microenvironment—dramatically improving local drug retention and bioavailability.
This breakthrough marks a shift in liposomal drug delivery from passive accumulation to controllable, trigger-based precision delivery. Litchlab stands at the forefront of this transformation.
As an innovation-driven company specializing in nanocarrier systems, Litchlab offers an end-to-end development solution for liposomal drugs—from formulation design → drug encapsulation → surface targeting → responsive mechanism engineering → IND translation → cGMP production.
A diverse range of ligands: antibody fragments, aptamers, RGD peptides, tumor-homing peptides, glycan ligands
Targeting key tumor biomarkers: PD-L1, HER2, αvβ3, EGFR, etc.
Enhances tumor accumulation by 5–10× on average
Utilizes efficient conjugation strategies: EDC/NHS, Click Chemistry, Maleimide-Thiol coupling
pH-sensitive: triggers drug release in acidic tumor environments (pH 5.5–6.5)
GSH-responsive: leverages elevated intracellular glutathione levels for intracellular release
Enzyme-responsive: MMP-2/9-mediated degradation of the liposomal matrix
Enables spatial and temporal control for maximizing therapeutic impact
Compatible with multiple production techniques: REV, thin-film dispersion, microfluidics
High encapsulation efficiency (>85%), particle sizes 80–150 nm, PDI < 0.2
Supports various payload types:
Small molecules: Paclitaxel, Doxorubicin, Cisplatin
Biologics: Interferons, monoclonal antibodies, proteases
Nucleic acids: siRNA, mRNA, CRISPR components
Radiopharmaceuticals: Lu-177, Zr-89, etc.
QbD-based process development and stability profiling
Fully compliant with FDA/EMA/NMPA regulations (ICH Q8/Q11)
Supports pilot to commercial-scale cGMP manufacturing, covering early clinical stages and tech transfer
Indication | Drug Type | Target Marker | Delivery System |
---|---|---|---|
Breast/Ovarian Cancer | Paclitaxel/Doxorubicin | HER2 / EGFR | Targeted Liposomes |
Liver/Pancreatic Cancer | Radiopharmaceuticals | αvβ3 / PD-L1 | RDC-Liposomes |
Respiratory Vaccines | mRNA / Adhesion Proteins | TLR Agonists | LNP Systems |
Gene Silencing Therapy | siRNA (e.g., PCSK9, KRAS) | ASGPR, Integrin | siRNA-Liposomes |
Precision drug delivery is no longer a distant vision—it’s happening now. By advancing its core technology framework in targeting ligands, microenvironmental responsiveness, and multimodal payload integration, Litchlab is empowering global pharma and biotech partners to translate liposomal drugs into tangible breakthroughs in oncology, immunotherapy, gene modulation, and beyond.
For more information, please feel free to contact us at:
E-Mail:RD2@Litchlab.com