4.3 Article

Synthesis of Multifunctional Organic Nanoparticles Combining Photodynamic Therapy and Chemotherapeutic Drug Release

Journal

MACROMOLECULAR RESEARCH
Volume 30, Issue 1, Pages 61-69

Publisher

POLYMER SOC KOREA
DOI: 10.1007/s13233-022-0021-0

Keywords

photodynamic therapy; chitosan; BODIPY; doxorubicin; drug release

Funding

  1. Sivas Cumhuriyet University Scientific Research Projects Commission (CUBAP) [M-697]

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This study synthesized chitosan and BODIPY-based nanoparticles capable of drug delivery and generating singlet oxygen, showing effective PDT properties on cancer cells with low toxicity.
Cancer is a group of diseases that are caused by uncontrolled proliferation of cells in various parts of the body and it is one of the most studied diseases worldwide. Photodynamic therapy (PDT) is a treatment that uses photosensitizers called photosensitizing agents in addition to light to kill cancer cells. Photosensitizers work only after they have been activated by certain types of light PDT contains three basic components, these are a photosensitizer, visible light and molecular oxygen (O-3(2)). The efficiency of the therapeutic action is directly related to the property of the photosensitizer. In this study, chitosan and BODIPY based nanoparticles that were capable of carrying out drug delivery and producing singlet oxygen (O-1(2)) were synthesized for the first time. For this purpose, organic nanoparticles showed PDT feature were synthesized via the formation of ionic complexes formed with opposite charged ionic interactions between the synthesized BODIPY derivative (PDT agent) and chitosan hydrochloride at appropriate pH (pH= 6). Later, during the formation of this ionic complex, a chemotherapeutic model drug (Doxorubicin) was added to the medium and chemotherapeutic drug-loaded chitosan and BODIPY-based nanoparticles were synthesized. Finally, while drug-free (Y1-Chitosan nanoparticles) and drug-loaded organic nanoparticles (Y1-Chitosan-Dox nanoparticles) showed very good PDT properties, they were found to be effective on MCF7 cancer cells and less toxic to L929 cells.

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