Radioresistance, a serious problem during radiotherapy (RT) caused by hypoxia, results in tumor relapse. Hemoglobin-based oxygen carriers (HBOCs) which can deliver oxygen, offer a promising option to cancer patients with radioresistance. However, the potential autoxidative cytotoxicity and renal toxicity of heme in hemoglobin (Hb) hamper their clinical application. Thus, here, a nano red blood cell (nnRBC) is fabricated that replaces heme with perfluorodecalin (FDC), a hydrophobic, high oxygen carrying fluorocarbon, and coated with membranes of RBCs. For the first time, nnRBCs provide a new method for the delivery of FDC since it cannot be emulsified by any FDA approved emulsifiers. nnRBCs encapsulate FDC with 8000% (w/w) drug loading efficiency and show superior storage stability within seven days. After intravenous delivery, nnRBCs reverse tumor hypoxia effectively compared with RT treatment alone. Of note, the components of nnRBCs are all from organisms or safe substances that have been verified by human testing, which gives nnRBCs great potential to rapidly enter into clinical trials.Radiotherapy (RT), as an effective treatment for solid tumors, is utilized in more than 60% cancer patients at present. [1,2] However, radio resistance resulting in tumor relapse must be solved for urgent need. [3][4][5] Abundant clinical data suggest that threefold radioresistance occurs on cells in hypoxia condition than welloxygenated cells. [6,7] Mechanism in this effect may involve further damage of DNA based on the reaction between molecular oxygen and DNA radicals induced in RT. [4,5,8] More severely, tumor hypoxia not only promotes damaged DNA repaired, but also