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半强度枸橼酸盐CPD及用于改善血液保存的新型添加剂溶液。I. 六种实验溶液的研究。

Half-strength citrate CPD and new additive solutions for improved blood preservation. I. Studies of six experimental solutions.

作者信息

Högman C F, Eriksson L, Gong J, Payrat J M, Debrauwere J

机构信息

Department of Clinical Immunology and Transfusion Medicine, University Hospital, Uppsala, Sweden.

出版信息

Transfus Med. 1993 Mar;3(1):43-50. doi: 10.1111/j.1365-3148.1993.tb00103.x.

DOI:10.1111/j.1365-3148.1993.tb00103.x
PMID:8038896
Abstract

Poor stability of plasma factor VIII in whole blood and loss of erythrocyte 2,3-bis-phosphoglycerate (BPG) during red cell storage are limitations with systems for blood component preparation in current use. This study presents attempts to improve post-collection storage conditions in both these respects using half-strength citrate CPD solution (0.5CPD) for blood collection, which has been shown by others to improve the stability of factor VIII, and some compositions of hypotonic additive solutions for red cell storage containing citrate, adenine, mannitol, and phosphate. Guanosine was also included in some of the media. The erythrocyte BPG concentration was maintained at a normal level for 3-4 weeks with the best of the tested compositions. Total adenine nucleotide concentration was maintained at the original level for 49 days and adenosine triphosphate for 28 days. Spontaneous storage haemolysis was low, 0.31% (mean) +/- 0.08-0.10% (SD) after 49 days in the two best compositions. The intracellular pH was 0.2-0.3 pH units higher than the extracellular pH at the beginning of storage, but this difference gradually diminished and disappeared after 4-5 weeks. We suggest two likely explanations of the effects: the maintenance of intracellular pH at a level sufficiently high not to impair BPG synthesis until after several weeks of storage, and a sufficient supply of phosphate needed in the synthesis of organic phosphate compounds. The content of citrate was selected such that the total amount supplied to a patient in a massive transfusion, when using a combination of 0.5CPD plasma and red cell suspension, would be smaller than that provided by a transfusion of CPD whole blood.

摘要

全血中血浆凝血因子VIII稳定性差以及红细胞储存期间红细胞2,3-二磷酸甘油酸(BPG)的丢失是目前使用的血液成分制备系统存在的局限性。本研究尝试在这两个方面改善采血后的储存条件,采用半强度枸橼酸盐CPD溶液(0.5CPD)进行血液采集,其他人已证明该溶液可提高因子VIII的稳定性,还尝试了一些用于红细胞储存的低渗添加剂溶液的成分,这些溶液含有枸橼酸盐、腺嘌呤、甘露醇和磷酸盐。部分培养基中还添加了鸟苷。在测试的最佳成分中,红细胞BPG浓度可维持在正常水平3 - 4周。总腺嘌呤核苷酸浓度在49天内维持在初始水平,三磷酸腺苷在28天内维持在初始水平。在两种最佳成分中,49天后自发储存溶血率较低,平均为0.31% +/- 0.08 - 0.10%(标准差)。储存开始时细胞内pH比细胞外pH高0.2 - 0.3个pH单位,但这种差异在4 - 5周后逐渐减小并消失。我们提出了两种可能的作用机制解释:在储存数周后将细胞内pH维持在足够高的水平,以免损害BPG合成;以及为有机磷酸盐化合物合成提供足够的磷酸盐供应。选择枸橼酸盐含量时,使得在大量输血时,当使用0.5CPD血浆和红细胞悬液组合时,输给患者的总量要小于输注CPD全血所提供的量。

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Half-strength citrate CPD and new additive solutions for improved blood preservation. I. Studies of six experimental solutions.半强度枸橼酸盐CPD及用于改善血液保存的新型添加剂溶液。I. 六种实验溶液的研究。
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