失血性休克
血红蛋白
基质
白蛋白
纳米颗粒
壳体(结构)
红细胞
休克(循环)
化学
材料科学
生物物理学
医学
纳米技术
免疫学
生物化学
内科学
生物
免疫组织化学
复合材料
作者
Natsumi Kohyama,Koki Takamine,Wataru Okamoto,Taiga Yamada,Masatoshi Yamaguchi,Mitsutomo Kohno,Ryota Tochinai,Teruyuki Komatsu
标识
DOI:10.1021/acsabm.4c01901
摘要
A wide array of artificial O2 carriers based on hemoglobin (Hb) has been developed to serve as substitutes for red blood cells (RBCs). Nevertheless, the prevention of heme-iron oxidation within Hb remains a critical challenge. In this study, we synthesized a nanoparticle O2 carrier comprising a polymerized stromal-free Hb (SFHb) core covered with a human serum albumin shell, designated as SFHbNP. With an optimized particle size of approximately 30 nm, SFHbNPs are engineered to evade uptake by the reticuloendothelial system in various organs. We characterized the physicochemical properties and biochemical functions of SFHbNPs, demonstrating that the incorporation of trace amounts of the antioxidant enzyme catalase within the core effectively suppresses Hb autoxidation. The SFHbNP solution exhibited excellent compatibility with human blood and demonstrated no cytotoxicity toward human endothelial cells. Moreover, its extended circulatory retention enabled preclinical evaluation in animal models. In a rat model of 50% hemorrhagic shock, administration of SFHbNP solution achieved full resuscitation, as evidenced by the restoration of circulatory parameters. Serum biochemistry tests and histopathological analyses of major organs indicated no adverse effects. Comprehensive in vitro and in vivo studies confirm the safety and potential efficacy of SFHbNPs as a promising RBC alternative in transfusion medicine.
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