2017 Fiscal Year Final Research Report
Radiosensitization effect of liposome-encapsulated fullerenes on human melanoma
Project/Area Number |
26390017
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Nanomaterials chemistry
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Research Institution | Mie University |
Principal Investigator |
Kato Shinya 三重大学, 地域イノベーション推進機構, 助教 (40545547)
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Co-Investigator(Kenkyū-buntansha) |
吉村 哲郎 三重大学, 工学研究科, 特任教授(研究担当) (30035472)
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Research Collaborator |
MIWA Nobuhiko 県立広島大学, 名誉教授
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Project Period (FY) |
2014-04-01 – 2018-03-31
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Keywords | リポソーム / フラーレン / 脂質過酸化 |
Outline of Final Research Achievements |
The polyhydroxy small-gap fullerenes (SGFs: C120O30(OH)30・30H2O・25Na+) were encapsulated in MLV liposomes (Lpsm) composed of DOPC and DOPS, which are designated as LpsmSGFs (DOPC/DOPS/SGFs = 35 mM:15 mM:246-445 μM, φ141.2 nm, ζ-potential-35.65 mV). Radiosensitization by LpsmSGFs under X-ray irradiation was evaluated on human melanoma HMV-II cells. On 7th day after X-ray irradiation, cell proliferation degree decreased on cells pretreated with LpsmSGFs than Lpsm or free-SGFs. LpsmSGFs obviously exhibited more augmented mitochondrial membrane potentials on perinuclear region of cells than Lpsm or free-SGFs. The oxidation-reduction potentials of SGFs aqueous solution increased by X-ray irradiation. These results suggest that LpsmSGFs-mediated generation of reactive oxygen species results in damages to cellular components such as mitochondria and DNA on cells, and thereby cell proliferation decreased. The LpsmSGFs has a potential as a pro-oxidative type radiosensitizer.
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Free Research Field |
応用生物化学
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