Abstract
In this paper, a novel synthesis of polyethylene glycol (PEG)-modified polypyrrole (PPy) nanomaterials is demonstrated by combining reversible addition-fragmentation chain transfer polymerization and oxidative polymerization. Dye molecules with a heat-labile linker are used as a model drug and covalently anchored onto the PEGlated PPy nanomaterials via "click chemistry." The strong absorption of such PPy nanomaterials in the near-infrared region endows the system excellent photothermal effect, which can be used not only as efficient photothermal agents for photothermal therapy but also good controllers of a drug-release system by retro D-A reaction. Polyethylene glycol (PEG) and pyrene-oxabicycloheptene-alkyne (POA)-modified PPy (PEG-POA PPy) nanomaterials are synthesized by combining reversible addition-fragmentation chain transfer polymerization and oxidative polymerization. Such nanomaterials can be used not only as efficient photothermal agents for photothermal therapy but also as a controller of a drug-release system by the retro D-A reaction under near-infrared irradiation.
| Original language | English |
|---|---|
| Pages (from-to) | 149-154 |
| Number of pages | 6 |
| Journal | Macromolecular Rapid Communications |
| Volume | 37 |
| Issue number | 2 |
| DOIs | |
| State | Published - 1 Jan 2016 |
Keywords
- NIR light
- PPy nanoparticles
- controlled-release
- photothermal effect
- retro D-A reaction