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Phonozen-mediated photodynamic therapy comparing two wavelengths in a mouse model of peritoneal carcinomatosis

Authors
 Hyoung-Il Kim  ;  Sung-Ho Lee  ;  Su-Jin Shin  ;  Jong-Hyun Park  ;  Jae Eun Yu  ;  Sang Won Lee  ;  Seung Hee Yang  ;  Layla Pires  ;  Brian C Wilson 
Citation
 PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES, Vol.22(11) : 2563-2572, 2023-11 
Journal Title
PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES
ISSN
 1474-905X 
Issue Date
2023-11
MeSH
Animals ; Cell Line, Tumor ; Disease Models, Animal ; Humans ; Mice ; Mice, Nude ; Necrosis ; Peritoneal Neoplasms* / drug therapy ; Photochemotherapy* / methods ; Photosensitizing Agents / pharmacology
Keywords
Mouse model ; Necrosis ; Peritoneal carcinomatosis ; Photodynamic therapy
Abstract
Background: This study assessed the therapeutic efficacy of intraperitoneal photodynamic therapy (PDT) using photosensitizer activation at two different wavelengths, 405 and 664 nm, in a mouse model of peritoneal carcinomatosis.

Methods: The dark and light cytotoxicity of chlorin e6-polyvinylpyrrolidone (Phonozen) were measured in vitro under 402 ± 14 and 670 ± 18 nm LED activation in bioluminescent human gastric cancer cells, MKN45-luc. Cell viability was measured at 6 h after irradiation using the PrestoBlue assay. Corresponding in vivo studies were performed in athymic nude mice by intraperitoneal injection of 1 × 106 MKN45-luc cells. PDT was performed 10 d after tumor induction and comprised intraperitoneal injection of Phonozen followed by light irradiation at 3 h, delivered by a diffusing-tip optical fiber placed in the peritoneal cavity and coupled to a 405 or 664 nm diode laser to deliver a total energy of 50 J (20 mice per cohort). Whole-body bioluminescence imaging was used to track the tumor burden after PDT out to 130 days, and 5 mice in each cohort were sacrificed at 4 h post treatment to measure the acute tumor necrosis.

Results: Photosensitizer dose-dependent photocytotoxicity was higher in vitro at 405 than 664 nm. In vivo, PDT reduced the tumor growth rate at both wavelengths, with no statistically significant difference. There was substantial necrosis, and median survival was significantly prolonged at both wavelengths compared with controls (46 and 46 vs. 34 days).

Conclusions: Phonozen-mediated PDT results in significant cytotoxicity in vitro as well as tumor necrosis and prolonged survival in vivo following intraperitoneal light irradiation. Blue light was more photocytotoxic than red in vitro and had marginally higher efficacy in vivo.
Full Text
https://link.springer.com/article/10.1007/s43630-023-00470-w
DOI
10.1007/s43630-023-00470-w
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Hyoung Il(김형일) ORCID logo https://orcid.org/0000-0002-6134-4523
Shin, Su Jin(신수진) ORCID logo https://orcid.org/0000-0001-9114-8438
Lee, Sang-Won(이상원) ORCID logo https://orcid.org/0000-0002-8038-3341
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/197582
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