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A simple method for activating the platelets used in microfluidic platelet aggregation tests: Stirring-induced platelet activation

High-shear stimulation is well known as one of the key factors affecting platelet activation and aggregation, which can lead to the formation of a thrombus. In one of our previous studies, we introduced migration distance-based platelet function analysis in a microfluidic system. In this study, we s...

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Autores principales: Lee, Hoyoon, Kim, Gyehyu, Lim, Chaeseung, Lee, ByoungKwon, Shin, Sehyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AIP Publishing LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5176351/
https://www.ncbi.nlm.nih.gov/pubmed/28058084
http://dx.doi.org/10.1063/1.4972077
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author Lee, Hoyoon
Kim, Gyehyu
Lim, Chaeseung
Lee, ByoungKwon
Shin, Sehyun
author_facet Lee, Hoyoon
Kim, Gyehyu
Lim, Chaeseung
Lee, ByoungKwon
Shin, Sehyun
author_sort Lee, Hoyoon
collection PubMed
description High-shear stimulation is well known as one of the key factors affecting platelet activation and aggregation, which can lead to the formation of a thrombus. In one of our previous studies, we introduced migration distance-based platelet function analysis in a microfluidic system. In this study, we set out to examine the effects of stirring on shear-induced platelet activation and aggregation in a chamber system by using a rotating stirrer. We found that the rotating stirrer caused not only rotational shear flow but also a strong radial secondary flow. The latter flow led to efficient mixing in the chamber. Moreover, the rotational flow led to the generation of shear stress, the magnitude of which can be controlled to activate the platelets. Activated platelets tend to aggregate themselves. The maximum platelet aggregation was observed at a critical shear rate of 3100 s(−1), regardless of the stirrer shape. Furthermore, the time taken to attain maximum aggregation was significantly shortened when using a wide stirrer (30 s) instead of a narrow one (180 s). When using a flat stirrer, the non-uniform shear field in the chamber system was resolved with the radial secondary flow-induced mixing; thus, most of the platelets were homogenously activated. The stirring-induced platelet activation mechanism was experimentally confirmed in a microfluidic system for a platelet aggregation test while monitoring the migration distance until the microfluidic channel is occluded. Our findings indicate that the present system, consisting of a rotating stirrer and a confined chamber, provides effective shear stimulation for activating platelets and inducing platelet aggregates.
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spelling pubmed-51763512017-01-05 A simple method for activating the platelets used in microfluidic platelet aggregation tests: Stirring-induced platelet activation Lee, Hoyoon Kim, Gyehyu Lim, Chaeseung Lee, ByoungKwon Shin, Sehyun Biomicrofluidics Regular Articles High-shear stimulation is well known as one of the key factors affecting platelet activation and aggregation, which can lead to the formation of a thrombus. In one of our previous studies, we introduced migration distance-based platelet function analysis in a microfluidic system. In this study, we set out to examine the effects of stirring on shear-induced platelet activation and aggregation in a chamber system by using a rotating stirrer. We found that the rotating stirrer caused not only rotational shear flow but also a strong radial secondary flow. The latter flow led to efficient mixing in the chamber. Moreover, the rotational flow led to the generation of shear stress, the magnitude of which can be controlled to activate the platelets. Activated platelets tend to aggregate themselves. The maximum platelet aggregation was observed at a critical shear rate of 3100 s(−1), regardless of the stirrer shape. Furthermore, the time taken to attain maximum aggregation was significantly shortened when using a wide stirrer (30 s) instead of a narrow one (180 s). When using a flat stirrer, the non-uniform shear field in the chamber system was resolved with the radial secondary flow-induced mixing; thus, most of the platelets were homogenously activated. The stirring-induced platelet activation mechanism was experimentally confirmed in a microfluidic system for a platelet aggregation test while monitoring the migration distance until the microfluidic channel is occluded. Our findings indicate that the present system, consisting of a rotating stirrer and a confined chamber, provides effective shear stimulation for activating platelets and inducing platelet aggregates. AIP Publishing LLC 2016-12-15 /pmc/articles/PMC5176351/ /pubmed/28058084 http://dx.doi.org/10.1063/1.4972077 Text en © 2016 Author(s). 1932-1058/2016/10(6)/064118/10 All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Regular Articles
Lee, Hoyoon
Kim, Gyehyu
Lim, Chaeseung
Lee, ByoungKwon
Shin, Sehyun
A simple method for activating the platelets used in microfluidic platelet aggregation tests: Stirring-induced platelet activation
title A simple method for activating the platelets used in microfluidic platelet aggregation tests: Stirring-induced platelet activation
title_full A simple method for activating the platelets used in microfluidic platelet aggregation tests: Stirring-induced platelet activation
title_fullStr A simple method for activating the platelets used in microfluidic platelet aggregation tests: Stirring-induced platelet activation
title_full_unstemmed A simple method for activating the platelets used in microfluidic platelet aggregation tests: Stirring-induced platelet activation
title_short A simple method for activating the platelets used in microfluidic platelet aggregation tests: Stirring-induced platelet activation
title_sort simple method for activating the platelets used in microfluidic platelet aggregation tests: stirring-induced platelet activation
topic Regular Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5176351/
https://www.ncbi.nlm.nih.gov/pubmed/28058084
http://dx.doi.org/10.1063/1.4972077
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