Investigation of titanium peroxide nanoparticles for cancer therapy application
Project/Area Number |
25420831
|
Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Biofunction/Bioprocess
|
Research Institution | Kobe University |
Principal Investigator |
OGINO Chiaki 神戸大学, 工学(系)研究科(研究院), 准教授 (00313693)
|
Co-Investigator(Kenkyū-buntansha) |
SASAKI Ryouhei 神戸大学, 医学(系)研究科(研究院), 教授 (30346267)
|
Project Period (FY) |
2013-04-01 – 2016-03-31
|
Project Status |
Completed (Fiscal Year 2015)
|
Budget Amount *help |
¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2015: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
|
Keywords | 放射線照射 / チタン酸化物 / 活性酸素種 / ナノ粒子 / がん治療 / 二酸化チタン / 過酸化チタン / がん細胞損傷 / 過酸化水素 |
Outline of Final Research Achievements |
Titanium peroxide nanoparticles (TiOxNPs) was synthesized and their efficacy as novel agents that can potently enhance the effects of radiation in the treatment of pancreatic cancer was investigated. The core structures of the PAA-TiOxNPs were found to be of the anatase type. The TiOxNPs and PAA-TiOxNPs showed a distinct ability to produce hydroxyl radicals in response to X-ray irradiation in a dose- and concentration-dependent manner, whereas the TiO2NPs did not. The combination of the PAATiOxNPs and X-ray irradiation induced significantly stronger tumor growth inhibition compared to treatment with either PAA-TiOxNPs or X-ray alone. In addition, bio-distribution of PAATiOx in Xenograft mouse model was identified, and the evaluation method of effect of X-ray irradiation on cell line was also established. Together these findings, TiOxNPs are potential agents for enhancing the effects of radiation on pancreatic cancer via hydroxyl radical production.
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Report
(4 results)
Research Products
(16 results)
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[Journal Article] Mutation of arginine residues to avoid non-specific cellular uptakes for hepatitis B virus core particles.2015
Author(s)
Mohamed suffian, I.F., Nishimura, Y., Morita,K., Nakamura-Tsuruta, S., Al-Jamal, K.T., Ishii, J., Ogino, C., Kondo, A.
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Journal Title
Journal of Nanobiotechnology
Volume: in press
Issue: 1
Pages: 0-0
DOI
Related Report
Peer Reviewed / Open Access / Acknowledgement Compliant
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[Journal Article] A display of pH-sensitive fusogenic GALA peptide facilitates endosomal escape from a bio-nanocapsule via an endocytic uptake pathway.2014
Author(s)
Nishimura, Y., Takeda, K., Ezawa, R., Ishii, J., Ogino, C., Kondo, A.
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Journal Title
Journal of Nanobiotechnology
Volume: 21(1)
Issue: 1
Pages: 11-11
DOI
Related Report
Peer Reviewed / Open Access / Acknowledgement Compliant
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