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Simultaneous assay of platelet adhesion at multiple shear rates within a single microfluidic channel
Zeng Lisha 1 * #,Yang Jun 2
1.Key Laboratory of Biorheological Science and Technology (Chongqing University), Ministry of Education, Bioengineering College, Chongqing University, Chongqing 400030, China
2.Bioengineering College, Chongqing University, Chongqing 400030, China
*Correspondence author
#Submitted by
Subject:
Funding: National Natural Science Foundation of China (No.Nos. 81371691, 31571005, 81501617), the Visiting Scholar Foundation of Key Laboratory of Biorheological Science and Technology)
Opened online: 8 April 2016
Accepted by: none
Citation: Zeng Lisha,Yang Jun.Simultaneous assay of platelet adhesion at multiple shear rates within a single microfluidic channel[OL]. [ 8 April 2016] http://en.paper.edu.cn/en_releasepaper/content/4682815
 
 
Cardiovascular diseases are currently the major causes of mortality in the world, especially in developed nations. As a predominant one, thrombosis is the platelet aggregation induced by a high shear rate. Platelet aggregation assay can clarify the occurrence mechanism of thrombosis, as well as used as an important tool in the clinical diagnosis, personalized treatment, and screening of anticoagulants. Thus, relevant studies attracted considerable attention. As an important step in platelet aggregation, platelet adhesion and its detection are also attracted intensive concern. Thus, some analytical methods have been developed for platelet adhesion assay, and the impact of shear rate is one of the focuses. Compared with other devices, biosensors can give a more accurate result within a shorter time. Furthermore, some biosensors can achieve real-time analysis. However, only one or several shear rates can be tested at the same time, which may decrease the analytical efficiency. Meanwhile, in most cases, only the average platelet-adhesion effect within a reactor is detection, and the impact of the distribution of shear rates is improperly neglected. In this study, a microfluidic device with a single channel is designed and fabricated for platelet adhesion assay. When the platelet-rich plasma flows through the collagen-modified sensing surface of the channel bottom, the interaction between platelets and collagen molecules on the entire surface can be simultaneously monitored by using a surface plasmon resonance imaging (SPRi) system. A gradient of the shear rate (0-546) could be formed within the channel by choosing a suitable depth-to-width ratio (1:5), so platelet adhesion at multiple shear rates could be monitored simultaneously. This method enables the measurement of the adhesion process of unlabeled platelets on the entire sensing surface, in vitro, at multiple shear rates. Such a system can obtain more accurate platelet adhesion result at a given shear rate than traditional methods. Furthermore, in an individual operation, platelet adhesion can be repeatedly tested at multiple points with an equal shear rate, so a much higher analytical efficiency can also be achieved.
Keywords:Biomedical engineering; Surface plasmon resonance imaging; Platelet aggregation; Biosensor; Microfluidics
 
 
 

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