Reactive oxygen species (ROS) generated by blood reperfusion to ischemic organs induce severe ischemia-reperfusion injury in marginal grafts, resulting in graft dysfunction. Removal of “bad” ROS generated during reperfusion is key to long-term graft survival, as it also increases the risk of graft failure in the chronic phase. Previous attempts to eliminate “bad” ROS using various antioxidants have failed because they also disrupt the redox response in normal cells, resulting in total cell death. The highly safe self-assembling antioxidant nanoparticles (redox nanoparticles, RNPs) we have developed can “selectively” remove the “bad” ROS produced during ischemia-reperfusion, thereby suppressing ischemia-reperfusion injury. The usefulness of RNP has been demonstrated not only in ischemia-reperfusion models such as cerebral infarction-reperfusion, but also in models of ulcerative colitis, dementia, and radiation injury, in which oxidative stress caused by ROS is the primary cause. Now that we have demonstrated the efficacy of RNPs in liver ischemia-reperfusion models, we plan to expand this study to the field of organ transplantation.
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