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猪血红蛋白作为人工氧载体——血影蛋白的潜在来源。

Swine hemoglobin as a potential source of artificial oxygen carriers, hemoglobin-vesicles.

机构信息

Artificial Red Cells Group, Waseda Bioscience Research Institute in Singapore (WABIOS), Biopolis, Singapore.

出版信息

Artif Cells Nanomed Biotechnol. 2013 Feb;41(1):37-41. doi: 10.3109/10731199.2012.716067. Epub 2012 Sep 19.

DOI:10.3109/10731199.2012.716067
PMID:22992176
Abstract

Hemoglobin-based oxygen carriers (HBOCs) have been developed as a transfusion alternative and oxygen therapy. The Hb source is usually outdated donated human blood or cow blood obtained from cattle industries because of its abundance. This study examined the feasibility of using swine Hb ((S)Hb) for preparation of cellular-type HBOCs, hemoglobin-vesicles (HbV). Purification of (S)Hb from fresh swine whole blood was conducted with processes including carbonylation ((S)HbO(2) --> (S)HbCO), pasteurization (60 °C, 15 hours) and tangential flow ultrafiltration, with yield of 90%. Actually, differential scanning calorimetric analysis showed a denaturation temperature of (S)HbCO at 83 °C and assures its stability during pasteurization. Concentrated (S)HbCO together with pyridoxal 5'-phosphate (PLP) as an allosteric effector was encapsulated in phospholipid vesicles to prepare (S)HbV. After decarbonylation ((S)HbCO --> (S)HbO(2)), the oxygen affinity (P(50)) of (S)Hb changes mainly by PLP, and the influence of Cl(-) was small, in a manner similar to that of human Hb ((H)Hb). However, after encapsulation, vesicles of (S)HbV showed much lower oxygen affinity (higher P(50)) than (H)HbV did. Autoxidation of (S)HbV was slightly faster than (H)HbV. Although some differences are apparent in oxygen affinity and autoxidation rates, results clarified that (S)Hb is useful as a starting material for HbV production.

摘要

血红蛋白基氧载体 (HBOCs) 已被开发为输血替代品和氧气治疗剂。Hb 来源通常是过时的捐赠人类血液或从牛产业获得的牛血液,因为其丰富。本研究考察了使用猪血红蛋白 ((S)Hb) 制备细胞型 HBOCs、血红蛋白囊泡 (HbV) 的可行性。从新鲜猪全血中纯化 (S)Hb 的过程包括碳化 ((S)HbO(2) --> (S)HbCO)、巴氏消毒 (60°C,15 小时) 和切向流超滤,产率为 90%。实际上,差示扫描量热法分析表明 (S)HbCO 的变性温度为 83°C,并确保其在巴氏消毒过程中的稳定性。将浓缩的 (S)HbCO 与吡哆醛 5'-磷酸 (PLP) 作为变构效应物一起包封在磷脂囊泡中制备 (S)HbV。脱碳化后 ((S)HbCO --> (S)HbO(2)),(S)Hb 的氧亲和力 (P(50)) 主要通过 PLP 改变,Cl(-) 的影响较小,与人类血红蛋白 ((H)Hb) 相似。然而,封装后,(S)HbV 的囊泡显示出比 (H)HbV 低得多的氧亲和力 (更高的 P(50))。(S)HbV 的自动氧化速度比 (H)HbV 略快。尽管在氧亲和力和自动氧化速率方面存在一些明显差异,但结果表明 (S)Hb 可用作 HbV 生产的起始材料。

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