4.7 Article

Glycyrrhetinic Acid-Modified Silicon Phthalocyanine for Liver Cancer-Targeted Photodynamic Therapy

Journal

BIOMACROMOLECULES
Volume 22, Issue 2, Pages 811-822

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.biomac.0c01550

Keywords

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Funding

  1. Basic Science Research Program through the National Research Foundation of Korea - Ministry of Science and ICT (MSIT) [NRF-2017R1A2B3010038]
  2. Catholic University of Korea

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A novel photosensitizer designed for liver cancer treatment using glycyrrhetinic acid has demonstrated significant therapeutic efficacy in liver cancer cells. The modified photosensitizer effectively accumulates in liver cancer and shows a tumor growth inhibition effect, suggesting its potential to alter conventional liver cancer treatment methods.
To supplement shortcomings of existing treatments and enhance the therapeutic effect for liver cancer, a novel photosensitizer is designed using silicon phthalocyanine (SiPC) and a unique targeting moiety, glycyrrhetinic acid (GA). The SiPC is modified with a hydrophilic polymer and finally bound with GA. The solubility, fluorescence, singlet oxygen generation, and UV-vis absorbance are analyzed, and receptor-dependent intracellular influx is estimated in various cell lines. Using flow cytometry and confocal microscopy, intracellular fluorescence was detected in liver cancer because of GA receptor overexpression. To prove in vitro photodynamic therapeutic effects, the sample treated cells are irradiated and viability of liver cancer cells decreases in proportion to laser power. Then, it is confirmed that GA-modified SiPC effectively accumulated in liver cancer of HepG2 tumor-bearing mouse. Additionally, the PDT-combined therapeutic effect of GA-modified SiPC is observed in the tumor model and shown to have a tumor growth inhibition effect (60.36 times higher than the control group) and supported by histological analyses. These results demonstrate that the newly modified SiPC can be applied to liver cancer-specific treatment with high therapeutic efficacy. Consequently, novel SiPC has the potential to alter conventional liver cancer-targeted therapy and chemotherapy in clinical use.

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