Temoporfin-Conjugated PEGylated Poly( N , N -dimethylacrylamide)-Coated Upconversion Colloid for NIR-Induced Photodynamic Therapy of Pancreatic Cancer.
Oleksandr ShapovalVitalii PatsulaDavid VětvičkaHana EngstováViktoriia OleksaMartina KabešováTaras VasylyshynPavla PoučkováVitalii PatsulaPublished in: Biomacromolecules (2024)
Photodynamic therapy (PDT) has the potential to cure pancreatic cancer with minimal side effects. Visible wavelengths are primarily used to activate hydrophobic photosensitizers, but in clinical practice, these wavelengths do not sufficiently penetrate deeper localized tumor cells. In this work, NaYF 4 :Yb 3+ ,Er 3+ ,Fe 2+ upconversion nanoparticles (UCNPs) were coated with polymer and labeled with meta -tetra(hydroxyphenyl)chlorin (mTHPC; temoporfin) to enable near-infrared light (NIR)-triggered PDT of pancreatic cancer. The coating consisted of alendronate-terminated poly[ N , N -dimethylacrylamide- co -2-aminoethylacrylamide]- graft -poly(ethylene glycol) [P(DMA-AEM)-PEG-Ale] to ensure the chemical and colloidal stability of the particles in aqueous physiological fluids, thereby also improving the therapeutic efficacy. The designed particles were well tolerated by the human pancreatic adenocarcinoma cell lines CAPAN-2, PANC-1, and PA-TU-8902. After intratumoral injection of mTHPC-conjugated polymer-coated UCNPs and subsequent exposure to 980 nm NIR light, excellent PDT efficacy was achieved in tumor-bearing mice.
Keyphrases
- photodynamic therapy
- fluorescence imaging
- clinical practice
- endothelial cells
- high glucose
- ionic liquid
- high fat diet induced
- induced pluripotent stem cells
- type diabetes
- estrogen receptor
- pluripotent stem cells
- skeletal muscle
- climate change
- insulin resistance
- quantum dots
- fluorescent probe
- visible light
- walled carbon nanotubes