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Pu-18-N-butylimide-NMGA-GNP conjugate is effective against hepatocellular carcinoma

BACKGROUND: Photodynamic therapy (PDT) is a new modality in the treatment of cancer. This study thus aims to examine whether the PDT is effective against in vivo hepatocellular carcinoma. METHODS: In vivo efficacy of PDT on hepatocellular carcinoma was tested in xenografted mice with human hepatocel...

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Detalles Bibliográficos
Autores principales: Kwon, Jin-Geun, Song, In-Sung, Kim, Min-Soo, Lee, Beom Hee, Kim, Jung Hwa, Yoon, Il, Shim, Young Key, Kim, Nari, Han, Jin, Youm, Jae Boum
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481715/
https://www.ncbi.nlm.nih.gov/pubmed/28664061
http://dx.doi.org/10.1016/j.imr.2013.05.001
Descripción
Sumario:BACKGROUND: Photodynamic therapy (PDT) is a new modality in the treatment of cancer. This study thus aims to examine whether the PDT is effective against in vivo hepatocellular carcinoma. METHODS: In vivo efficacy of PDT on hepatocellular carcinoma was tested in xenografted mice with human hepatocellular carcinoma cell lines (Huh7) by utilizing a gold nanoparticles (GNPs) conjugate of new photosensitizer (PS), purpurin-18-N-butylimide-N-methyl-D-glucamine (Pu-18-N-butylimide-NMGA). The conjugate (PS-GNPs) was synthesized from the reaction between Pu-18-N-butylimide-NMGA and chloroauric acid (HAuCl4). Mice were arbitrarily assigned into one of three groups. First group received saline alone, second group received PS-GNPs alone, and the last group received both PS-GNPs and irradiation. PS-GNPs was injected directly into the tumor mass and irradiations were performed 24 hours after injection of PS-GNPs. RESULTS: Tumor volume was significantly smaller in the group which received both PS-GNPs and irradiation compared with other two groups. Western blot and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay revealed that the group which received both PS-GNPs and irradiation showed larger amount of apoptotic protein and DNA fragmentation compared with other two groups. CONCLUSION: This study suggests that Pu-18-N-butylimide-NMGA-GNP conjugate is an effective agent for PDT in the treatment of hepatocellular carcinoma.