School of Engineering and Built Environment, Griffith University, Queensland, Australia; Critical Care Research Group, The Prince Charles Hospital, Queensland, Australia; Faculty of Medicine, University of Queensland, Queensland, Australia.
Menzies Health Institute Queensland, Griffith University, Queensland, Australia.
J Biomech. 2022 Jan;130:110898. doi: 10.1016/j.jbiomech.2021.110898. Epub 2021 Dec 6.
Despite decades of technological advancements in blood-contacting medical devices, complications related to shear flow-induced blood trauma are still frequently observed in clinic. Blood trauma includes haemolysis, platelet activation, and degradation of High Molecular Weight von Willebrand Factor (HMW vWF) multimers, all of which are dependent on the exposure time and magnitude of shear stress. Specifically, accumulating evidence supports that when blood is exposed to shear stresses above a certain threshold, blood trauma ensues; however, it remains unclear how various constituents of blood are affected by discrete shears experimentally. The aim of this study was to expose blood to discrete shear stresses and evaluate blood trauma indices that reflect red cell, platelet, and vWF structure. Citrated human whole blood (n = 6) was collected and its haematocrit was adjusted to 30 ± 2% by adding either phosphate buffered saline (PBS) or polyvinylpyrrolidone (PVP). Viscosity of whole blood was adjusted to 3.0, 12.5, 22.5 and 37.5 mPa·s to yield stresses of 3, 6, 9, 12, 50, 90 and 150 Pa in a custom-developed shearing system. Blood samples were exposed to shear for 0, 300, 600 and 900 s. Haemolysis was measured using spectrophotometry, platelet activation using flow cytometry, and HMW vWF multimer degradation was quantified with gel electrophoresis and immunoblotting. For tolerance to 300, 600 and 900 s of exposure time, the critical threshold of haemolysis was reached after blood was exposed to 90 Pa for 600 s (P < 0.05), platelet activation and HMW vWF multimer degradation were 50 Pa for 600 s and 12 Pa for 300 s respectively (P < 0.05). Our experimental results provide simultaneous comparison of blood trauma indices and thus also the relation between shear duration and magnitude required to induce damage to red cells, platelets, and vWF. Our results also demonstrate that near-physiological shear stress (<12 Pa) is needed in order to completely avoid any form of blood trauma. Therefore, there is an urgent need to design low shear-flow medical devices in order to avoid blood trauma in this blood-contacting medical device field.
尽管在接触血液的医疗器械领域已经取得了几十年的技术进步,但与切变流引起的血液创伤相关的并发症在临床上仍经常观察到。血液创伤包括溶血、血小板激活和高分子量 von Willebrand 因子 (HMW vWF) 多聚体的降解,所有这些都取决于暴露时间和切变应力的大小。具体而言,越来越多的证据表明,当血液暴露于超过一定阈值的切变应力时,就会发生血液创伤;然而,目前尚不清楚血液的各种成分是如何受到实验中离散切变的影响的。本研究的目的是使血液暴露于离散切变应力下,并评估反映红细胞、血小板和 vWF 结构的血液创伤指数。收集柠檬酸化的人全血(n=6),并通过添加磷酸盐缓冲盐水(PBS)或聚乙烯吡咯烷酮(PVP)将其血细胞比容调整至 30±2%。全血的粘度调整至 3.0、12.5、22.5 和 37.5 mPa·s,以在定制的剪切系统中产生 3、6、9、12、50、90 和 150 Pa 的应力。血液样本暴露于剪切力下 0、300、600 和 900 s。使用分光光度法测量溶血,使用流式细胞术测量血小板激活,使用凝胶电泳和免疫印迹定量测量 HMW vWF 多聚体降解。对于 300、600 和 900 s 的暴露时间耐受,在血液暴露于 90 Pa 600 s 后达到溶血的临界阈值(P<0.05),血小板激活和 HMW vWF 多聚体降解分别在 50 Pa 600 s 和 12 Pa 300 s(P<0.05)。我们的实验结果提供了血液创伤指数的同时比较,因此也提供了引起红细胞、血小板和 vWF 损伤所需的剪切持续时间和大小之间的关系。我们的结果还表明,需要接近生理的剪切应力(<12 Pa)才能完全避免任何形式的血液创伤。因此,迫切需要设计低剪切流医疗器械,以避免在这个接触血液的医疗器械领域发生血液创伤。