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提高凝血因子 VIII 产量的可能性

[Possibilities to elevate the factor VIII yield].

作者信息

Uteg K H, Tausendfreund K

出版信息

Folia Haematol Int Mag Klin Morphol Blutforsch. 1987;114(1):153-69.

PMID:2439416
Abstract

By referring initially to remarks about the structure and function of the coagulation factor VIII and about the manufacture and demand for preparations for the substitution treatment in patients affected with haemophilia A, possibilities are presented how to increase the collection of factor VIII by applying intensive measures. These involve the impact on the basic material (including donors) as well as process variables within the range of plasma collection and process technique. On the basis of own research results and data from literature the following measures can be introduced and evaluated as far as their effect on the collection of factor VIII is concerned: Donor testing, selection: increased by 25% approximately Plasmapheresis, blood bags: (prerequisite for certain technological measures) Thawing technique: increase by 20-30% approximately (thaw siphon) Citrate-free anticoagulant: increase by 30% approximately (e.g. heparin) Donor conditioning: increased by 200-400% approximately (DDAVP) The establishment of possible and reasonable combinations of measures can contribute to intensify the collection of factor VIII. The advantages to be expected are mentioned. The level of gene-technological collection of factor VIII is dealt with prospectively.

摘要

通过首先提及有关凝血因子VIII的结构和功能以及甲型血友病患者替代治疗制剂的生产和需求的论述,展示了如何通过采取强化措施来增加因子VIII的采集量。这些措施涉及对基础材料(包括献血者)的影响以及血浆采集范围内的过程变量和工艺技术。根据自身研究结果和文献数据,就其对因子VIII采集的影响而言,可引入并评估以下措施:献血者检测、选择:大约增加25%;血浆置换、血袋:(某些技术措施的前提条件);解冻技术:大约增加20 - 30%(解冻虹吸管);无枸橼酸盐抗凝剂:大约增加30%(如肝素);献血者预处理:大约增加200 - 400%(去氨加压素)。建立可行且合理的措施组合有助于强化因子VIII的采集。文中提到了预期的优势。前瞻性地探讨了因子VIII基因技术采集的水平。

相似文献

1
[Possibilities to elevate the factor VIII yield].提高凝血因子 VIII 产量的可能性
Folia Haematol Int Mag Klin Morphol Blutforsch. 1987;114(1):153-69.
2
Cryoprecipitate of intermediate purity produced in a closed thaw-siphon system from DDAVP stimulated blood donor plasma.在封闭的解冻虹吸系统中,由去氨加压素刺激的献血者血浆制备的中等纯度冷沉淀。
Folia Haematol Int Mag Klin Morphol Blutforsch. 1990;117(4):565-70.
3
Production of cryoprecipitate of intermediate purity in a closed system thaw-siphon process.在封闭系统解冻虹吸过程中生产中等纯度的冷沉淀。
Thromb Haemost. 1981 Aug 28;46(2):543-6.
4
[Donor selection for the production of factor XIII preparations].[用于制备凝血因子 XIII 制剂的供体选择]
Folia Haematol Int Mag Klin Morphol Blutforsch. 1985;112(3):447-55.
5
[Production of factor VIII preparations and their use in the substitution therapy of hemophilia A].
Z Gesamte Inn Med. 1982 Oct 1;37(19):641-4.
6
In vivo characteristics of thaw siphon cryoprecipitate compared to other factor VIII preparations.与其他凝血因子 VIII 制剂相比,解冻虹吸冷沉淀的体内特性。
Thromb Haemost. 1980 Feb 29;43(1):25-7.
7
Cold storage of citrated whole blood induces drastic time-dependent losses in factor VIII and von Willebrand factor: potential for misdiagnosis of haemophilia and von Willebrand disease.枸橼酸盐全血的冷藏会导致凝血因子 VIII 和血管性血友病因子随时间急剧减少:存在血友病和血管性血友病疾病误诊的可能性。
Blood Coagul Fibrinolysis. 2006 Jan;17(1):39-45. doi: 10.1097/01.mbc.0000198990.16598.85.
8
Plasma exchange donation of cryoprecipitate after DDAVP stimulation: an alternative source of factor VIII.
Prog Clin Biol Res. 1990;324:189-98.
9
Use of plasma with high levels of ionised calcium in the production of model scale coagulation factor concentrates.在生产模型规模的凝血因子浓缩物中使用高离子钙水平的血浆。
Thromb Haemost. 1990 Nov 30;64(3):374-8.
10
An improved thaw-siphon method for the cryoprecipitate preparation.一种改进的用于制备冷沉淀的解冻虹吸法。
Vox Sang. 1980;38(3):172-7.