Cationic BODIPY Photosensitizers for Mitochondrion-Targeted Fluorescence Cell-Imaging and Photodynamic Therapy.
Isabel Wen BadonJun-Pil JeeTemmy Pegarro ValesChanwoo KimSeungbin LeeJaesung YangSi Kyung YangHo-Joong KimPublished in: Pharmaceutics (2023)
The straightforward synthesis of three cationic boron-dipyrromethene (BODIPY) derivatives and their mitochondria-targeting and photodynamic therapeutic (PDT) capabilities are reported. Two cancer cell lines (HeLa and MCF-7) were used to investigate the PDT activity of the dyes. Compared to their non-halogenated counterparts, halogenated BODIPY dyes exhibit lower fluorescence quantum yields and enable the efficient production of singlet oxygen species. Following LED light irradiation at 520 nm, the synthesized dyes displayed good PDT capabilities against the treated cancer cell lines, with low cytotoxicity in the dark. In addition, functionalization of the BODIPY backbone with a cationic ammonium moiety enhanced the hydrophilicity of the synthesized dyes and, consequently, their uptake by the cells. The results presented here collectively demonstrate the potential of cationic BODIPY-based dyes as therapeutic drugs for anticancer photodynamic therapy.
Keyphrases
- photodynamic therapy
- fluorescent probe
- living cells
- fluorescence imaging
- papillary thyroid
- aqueous solution
- single molecule
- cancer therapy
- energy transfer
- cell cycle arrest
- squamous cell
- high resolution
- cell death
- lymph node metastasis
- single cell
- cell therapy
- squamous cell carcinoma
- stem cells
- childhood cancer
- mesenchymal stem cells
- molecular dynamics
- bone marrow
- cell proliferation
- young adults
- mass spectrometry
- newly diagnosed
- reactive oxygen species
- genetic diversity
- drug delivery
- oxidative stress
- human health
- monte carlo