Sulfur dioxide (SO 2 ) based gas therapy has received great attention recently. Nevertheless, it is still a challenge to fabricate a SO 2 delivery system to achieve effective delivery and on-demand stimuli triggered release at tumor sites. Herein, a chain-shattering polymeric SO 2 prodrug micelle system was fabricated for effective SO 2 based gas therapy. First, an amphiphilic polymer (mPEG-P(HDI-DN)) was prepared by polycondensation of poly(ethylene glycol) methyl ether, hexamethylene diisocyanate and monomer containing SO 2 . mPEG-P(HDI-DN) can self-assemble into spherical micelles with a diameter of around 50-90 nm. Triggered release of SO 2 from micelles can be achieved in the presence of GSH with the degradation of mPEG-P(HDI-DN) into small molecules. The in vitro experiment proved that mPEG-P(HDI-DN) micelles can enter into osteosarcoma cells and inhibit the growth of osteosarcoma cells by increasing the ROS level in cells. The in vivo experiments demonstrate that mPEG-P(HDI-DN) micelles can inhibit the growth of osteosarcoma effectively without obvious tissue toxicity. These results indicate that this chain-shattering polymeric SO 2 prodrug micelle system is a promising candidate for effective SO 2 based gas therapy.
Keyphrases
- drug release
- cancer therapy
- drug delivery
- induced apoptosis
- cell cycle arrest
- room temperature
- endoplasmic reticulum stress
- oxidative stress
- stem cells
- signaling pathway
- dna damage
- cell proliferation
- pi k akt
- cell therapy
- carbon dioxide
- mesenchymal stem cells
- optical coherence tomography
- solid phase extraction
- bone marrow
- replacement therapy