2015 Fiscal Year Final Research Report
Prolonged functional lifespan of artificial red cells by using the electron energies produced by erythrocyte glycolysis
Project/Area Number |
25282136
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Partial Multi-year Fund |
Section | 一般 |
Research Field |
Biomedical engineering/Biomaterial science and engineering
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Research Institution | Nara Medical University |
Principal Investigator |
SAKAI HIROMI 奈良県立医科大学, 医学部, 教授 (70318830)
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Project Period (FY) |
2013-04-01 – 2016-03-31
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Keywords | 人工酸素運搬体 / 人工赤血球 / リポソーム / ヘモグロビン / 電子伝達物質 / メトヘモグロビン / 輸血代替 |
Outline of Final Research Achievements |
In vivo safety and efficacy of artificial red cells (Hb-vesicles, Hb-V) as a transfusion alternative have been clarified extensively. Gradual autoxidation of ferrous Hb in Hb-V to form ferric metHb is inevitable and results in decreased oxygen carrying capacity. We found that metHb in Hb-V can be reduced to ferrous Hb by using the electron energies produced by erythrocyte glycolysis, via methylene blue as a transmembrane electron mediator. We tested other 14 candidate mediators, and found some other potential molecules that can reduce metHb effectively, as did methylene blue. The requisite chemical properties as a potential electron mediator are clarified. We established an indirect enzymatic metHb reducing system for Hb-V using unlimited endogenous electrons created in RBCs in combination with an effective electron mediator that prolongs the functional lifespan of HbV in blood circulation.
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Free Research Field |
人工赤血球
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