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通过血小板单采术采集的经病原体灭活技术(Mirasol®)处理的血小板不同制备程序的评估。

Evaluation of Different Preparation Procedures of Pathogen Reduction Technology(Mirasol®)-Treated Platelets Collected by Plateletpheresis.

作者信息

Janetzko Karin, Hinz Katharina, Marschner Susanne, Goodrich Ray, Klüter Harald

机构信息

Institute of Transfusion Medicine and Immunology, Red Cross Service of Baden-Württemberg - Hessen, Medical Faculty of Mannheim, Heidelberg University, Mannheim, Germany.

出版信息

Transfus Med Hemother. 2009;36(5):309-315. doi: 10.1159/000230038. Epub 2009 Aug 7.

Abstract

SUMMARY

BACKGROUND: The Mirasol® pathogen reduction technology (PRT) for platelet concentrates (PC) uses riboflavin and UV light (270-360 nm). We evaluated the impact of PRT on platelets in comparison to standard single-donor PC. MATERIAL AND METHODS: Platelets were resuspended in autologous plasma. After 2 h rest without agitation, PC were split into an untreated control unit (C-PC) and an immediately treated unit (T-PC) (series I). In series IV, split PC were stored under agitation over night before PRT was carried out. Platelet quality was assessed by pH, glucose consumption, lactate production rate, LDH, soluble sCD62p and CD62p expression with and without TRAP (thrombin receptor-activating peptide) over 7 days. RESULTS: SERIES I: On day 5, pH values were lower for T-PC (6.8 ± 0.2 vs. 7.4 ± 0.1, C-PC), accompanied by a higher glucose consumption rate of 0.069 ± 0.016 vs. 0.035 ± 0.006 mmol/10(12) platelets/h and lactate production rate of 0.126 ± 0.031 vs. 0.063 ± 0.011 mmol/10(12) platelets/h. CD62p using TRAP was lower for T-PC (50 ± 11 vs. 62 ± 14%). Baseline activation was higher in T-PC (35 ± 12 vs. 28 ± 15%). Longer initial rest time had no impact on these results (series II/III/IV). CONCLUSION: PRT leads to an increase of platelet metabolism and activation independent of the length of the initial rest times. PC resuspended in autologous plasma should be stored at maximum up to day 5.

摘要

摘要

背景:用于血小板浓缩物(PC)的Mirasol®病原体灭活技术(PRT)使用核黄素和紫外线(270 - 360纳米)。我们将PRT对血小板的影响与标准单采血小板浓缩物进行了比较。材料与方法:血小板重悬于自体血浆中。在无搅拌的情况下静置2小时后,将血小板浓缩物分为未处理的对照单元(C - PC)和立即处理的单元(T - PC)(系列I)。在系列IV中,分离后的血小板浓缩物在搅拌下过夜储存,然后进行PRT处理。通过pH值、葡萄糖消耗、乳酸产生率、乳酸脱氢酶(LDH)、可溶性sCD62p以及有无凝血酶受体激活肽(TRAP)刺激下的CD62p表达来评估血小板质量,观察期为7天。结果:系列I:在第5天,T - PC的pH值较低(6.8±0.2 vs. 7.4±0.1,C - PC),同时葡萄糖消耗率较高,分别为0.069±0.016 vs. 0.035±0.006 mmol/10¹²血小板/小时,乳酸产生率为0.126±0.031 vs. 0.063±0.011 mmol/10¹²血小板/小时。使用TRAP刺激后,T - PC的CD62p较低(50±11 vs. 62±14%)。T - PC的基线激活水平较高(35±12 vs. 28±15%)。更长的初始静置时间对这些结果无影响(系列II/III/IV)。结论:PRT导致血小板代谢和激活增加,且与初始静置时间长短无关。重悬于自体血浆中的血小板浓缩物最多应保存至第5天。

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