TY - JOUR
T1 - Discrete responses of erythrocytes, platelets, and von Willebrand factor to shear
AU - Chan, Chris H.H.
AU - Simmonds, Michael J.
AU - Fraser, Katharine H.
AU - Igarashi, Kosuke
AU - Ki, Katrina K.
AU - Murashige, Tomotaka
AU - Joseph, Mary T.
AU - Fraser, John F.
AU - Tansley, Geoff D.
AU - Watanabe, Nobuo
N1 - Funding Information:
The authors would like to recognise the financial assistance provided by The Prince Charles Hospital Foundation Team Grant (TM2017-04) and the ACTIONS National Health and Medical Research Council Centre for Research Excellence (APP1079421). Chris H.H. Chan is supported by The Prince Charles Hospital Foundation Research Fellowship (RF2019-02). Nobuo Watanabe received financial grant from the Japan Society for Promotion of Science (JSPS; KAKENHI JP17K01370 and JP20K12609).
Funding Information:
Thanks to Antony P. McNamee, Jacob Turner, Kieran Richardson, Ian Chu and Zoe Sever for technical support. We thanks to Tokyo Titanium Co. Ltd. Saitama, Japan for their kind support with surface roughness measurement. The authors would like to recognise the financial assistance provided by The Prince Charles Hospital Foundation Team Grant (TM2017-04) and the ACTIONS National Health and Medical Research Council Centre for Research Excellence (APP1079421). Chris H.H. Chan is supported by The Prince Charles Hospital Foundation Research Fellowship (RF2019-02). Nobuo Watanabe received financial grant from the Japan Society for Promotion of Science (JSPS; KAKENHI JP17K01370 and JP20K12609).
Publisher Copyright:
© 2021 The Authors
PY - 2022/1
Y1 - 2022/1
N2 - 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.
AB - 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.
KW - Blood-shearing device
KW - Exposure time
KW - HMW vWF multimer degradation
KW - Haemolysis
KW - Platelet activation
KW - Shear stress
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U2 - 10.1016/j.jbiomech.2021.110898
DO - 10.1016/j.jbiomech.2021.110898
M3 - Article
C2 - 34896790
AN - SCOPUS:85120986548
SN - 0021-9290
VL - 130
JO - Journal of Biomechanics
JF - Journal of Biomechanics
M1 - 110898
ER -