Photodynamic therapy (PDT) can destroy tumor cells by generating singlet oxygen (O) under light irradiation, which is limited by the hypoxia of the neoplastic tissue. Chemodynamic therapy (CDT) can produce toxic hydroxyl radical (⋅OH) to eradicate tumor cells by catalytic decomposition of endogenous hydrogen peroxide (HO), the therapeutic effect of which is highly dependent on the concentration of HO. Herein, we propose a BODIPY-ferrocene conjugate with a balanced O and ⋅OH generation capacity, which can serve as a high-efficiency antitumor agent by combining PDT and CDT. The ferrocene moieties endow the as-prepared conjugates with the ability of chemodynamic killing of tumor cells. Moreover, combined PDT/CDT therapy with improved antitumor efficiency can be realized after exposure to light irradiation. Compared with the monotherapy by PDT or CDT, the BODIPY-ferrocene conjugates can significantly increase the intracellular ROS levels of the tumor cells after light irradiation, thereby inducing the tumor cell apoptosis at low drug doses. In this way, a synergistic antitumor treatment is achieved by the combination of PDT and CDT.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/chem.202401916 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!