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通过鼻腔给予血管加压素类似物刺激供血者所制备的凝血因子VIII浓缩物。

Factor VIII concentrate prepared from blood donors stimulated by intranasal administration of a vasopressin analogue.

作者信息

Mikaelsson M, Nilsson I M, Vilhardt H, Wiechel B

出版信息

Transfusion. 1982 May-Jun;22(3):229-33. doi: 10.1046/j.1537-2995.1982.22382224947.x.

Abstract

With an interval of eight weeks between collections, blood was drawn twice from 120 blood donors. At one of the donations, 0.25 ml of synthetic vasopressin, (DDAVP, 1300 micrograms/ml), was administered intranasally 60 minutes prior to collection of the blood. No drug was given at the other donation. The yield of factor VIII clotting activity (VIII:C) and factor VIII antigen (VIIIR:Ag) was compared in blood drawn from the treated and untreated donors. To prevent degradation of VIII:C by fibrinolysis, tranexamic acid was added to the plasma from treated donors immediately after separation from the red blood cells. Plasma from treated donors and the derived Cohn fraction I-O contained approximately twice as much VIII:C as plasma and fraction I-O from untreated control donors. The concentration of VIIIR: Ag was also increased in fraction I-O made from plasma from treated donors, however to a lesser degree. The in vivo properties of factor VIII concentrates made from each group of donors were studied. Half-life in plasma and recovery of VIII:C were identical. Thus, intranasal synthetic vasopressin may be used to increase the yield of VIII:C in production of factor VIII concentrates.

摘要

在两次采血之间间隔八周的情况下,从120名献血者身上采集了两次血液。在其中一次献血时,在采血前60分钟经鼻给予0.25毫升合成血管加压素(去氨加压素,1300微克/毫升)。另一次献血时未给药。比较了从接受治疗和未接受治疗的献血者采集的血液中因子VIII凝血活性(VIII:C)和因子VIII抗原(VIIIR:Ag)的产量。为防止VIII:C因纤维蛋白溶解而降解,在从红细胞分离后立即向接受治疗的献血者的血浆中添加氨甲环酸。接受治疗的献血者的血浆及衍生的考恩I-O组分中所含的VIII:C约为未接受治疗的对照献血者的血浆和I-O组分的两倍。由接受治疗的献血者的血浆制成的I-O组分中VIIIR:Ag的浓度也有所增加,但程度较小。研究了每组献血者制成的因子VIII浓缩物的体内特性。血浆半衰期和VIII:C的回收率相同。因此,经鼻给予合成血管加压素可用于提高因子VIII浓缩物生产中VIII:C的产量。

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