Direct Functionalization of Polysaccharide-Based Xylan Phenyl Carbonate Nanoparticles with Tumor Cell Specific Antibodies.
Vrouyr BilemjianYusheng LinWei WanGabriella EgriGerwin HulsThomas HeinzeEdwin BremerMartin GerickeLars DähnePublished in: Chembiochem : a European journal of chemical biology (2024)
An efficient and easy-to-use approach is presented for obtaining biocompatible polysaccharide-based nanoparticles (NP) that can act as tumor-specific drug delivery agents. Two antibodies are directly immobilized onto reactive xylan phenyl carbonate (XPC) NP; namely Cetuximab (CTX) that binds to human epidermal growth factor receptor (EGFR) and Atezolizumab (ATZ) that binds to programmed death-ligand 1 (PD-L1). High coupling efficiency (up to 100 %) are achieved without any pre-activation and no aggregation occurs during antibody immobilization. By quartz crystal microbalance experiments with dissipation monitoring (QCM-D), flow cytometry assays, and confocal laser scanning microscopy imaging it is demonstrated that the functionalized XPC-NP specifically bind to cells carrying the corresponding antigens. Moreover, the NP retain the antibody specific bioactivities (growth inhibition for CTX and induction of T-cell cytotoxicity for ATZ).
Keyphrases
- immune response
- epidermal growth factor receptor
- flow cytometry
- high resolution
- tyrosine kinase
- drug delivery
- advanced non small cell lung cancer
- small cell lung cancer
- endothelial cells
- high throughput
- induced apoptosis
- klebsiella pneumoniae
- single cell
- high speed
- ionic liquid
- cell cycle arrest
- escherichia coli
- squamous cell carcinoma
- drug release
- quantum dots
- cancer therapy
- induced pluripotent stem cells
- photodynamic therapy
- multidrug resistant
- room temperature
- water soluble
- mesenchymal stem cells
- metastatic colorectal cancer
- tandem mass spectrometry