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首页> 外文期刊>Scientific reports. >Safety Evaluation of Hemoglobin-Albumin Cluster “HemoAct” as a Red Blood Cell Substitute
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Safety Evaluation of Hemoglobin-Albumin Cluster “HemoAct” as a Red Blood Cell Substitute

机译:血红蛋白-白蛋白簇“ HemoAct”作为红细胞替代品的安全性评估

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摘要

A hemoglobin (Hb) wrapped covalently by human serum albumins (HSAs), a core–shell structured hemoglobin-albumin cluster designated as “HemoAct”, is an O2-carrier designed for use as a red blood cell (RBC) substitute. This report describes the blood compatibility, hemodynamic response, and pharmacokinetic properties of HemoAct, and then explains its preclinical safety. Viscosity and blood cell counting measurements revealed that HemoAct has good compatibility with whole blood. Intravenous administration of HemoAct into anesthetized rats elicited no unfavorable increase in systemic blood pressure by vasoconstriction. The half-life of 125I-labeled HemoAct in circulating blood is markedly longer than that of HSA. Serum biochemical tests conducted 7 days after HemoAct infusion yielded equivalent values to those observed in the control group with HSA. Histopathologic inspections of the vital organs revealed no marked abnormality in their tissues. All results indicate that HemoAct has sufficient preclinical safety as an alternative material for RBC transfusion.
机译:由人血清白蛋白(HSA)共价包裹的血红蛋白(Hb)是一种设计为用作红血的O 2 载体,是一种由核-壳结构组成的血红蛋白-白蛋白簇,称为“ HemoAct”。单元(RBC)替代。该报告描述了HemoAct的血液相容性,血液动力学反应和药代动力学特性,然后解释了其临床前安全性。粘度和血细胞计数测量表明,HemoAct与全血具有良好的相容性。对麻醉的大鼠静脉内注射HemoAct不会引起血管收缩引起的全身血压升高。 125 I标记的HemoAct在循环血液中的半衰期明显长于HSA。 HemoAct输注后7天进行的血清生化测试得出的值与使用HSA的对照组中观察到的值相同。对重要器官的组织病理学检查未发现其组织明显异常。所有结果表明,HemoAct作为RBC输注的替代材料具有足够的临床前安全性。

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