| Project/Area Number |
21591600
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Radiation science
|
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| Research Institution | Kansai Medical University |
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Principal Investigator |
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| Co-Investigator(Kenkyū-buntansha) |
KARIYA Shuji 関西医科大学, 医学部, 講師 (40368220)
TANIGAWA Noboru 関西医科大学, 医学部, 准教授 (90227215)
NAKATANI Miyuki 関西医科大学, 医学部, 助教 (10533424)
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| Project Period (FY) |
2009 – 2011
|
| Project Status |
Completed (Fiscal Year 2011)
|
| Budget Amount *help |
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2011: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2010: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2009: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
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| Keywords | マイクロバブル / 炭酸ガス / 塞栓術 / 腫瘍学 / インターベンション / 塞栓剤 / 癌 / 放射線診断学 / TAE |
|---|
| Research Abstract |
CO2 microbubble can become an embolic material. In the swine, a renal artery could be embolized using the CO2 microbubble, and then the artery was recanalized in a short time. Thus, the CO2 microbubble can become an ultra short acting embolic material, and has the possibility that the organ to which the embolization is assumed to be a contraindication can be applied.
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