The MICELI (MICrofluidic, ELectrical, Impedance): Prototyping a Point-of-Care Impedance Platelet Aggregometer
Author
Roka-Moiia, YanaBozzi, Silvia
Ferrari, Chiara
Mantica, Gabriele
Dimasi, Annalisa
Rasponi, Marco
Santoleri, Andrea
Scavone, Mariangela
Consolo, Filippo
Cattaneo, Marco
Slepian, Marvin J
Redaelli, Alberto

Affiliation
Univ Arizona, Coll Med, Dept MedIssue Date
2020-02-11Keywords
electrical impedancePlatelet Aggregation
platelet function testing
point-of-care
whole blood aggregometry
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Roka-Moiia, Y.; Bozzi, S.; Ferrari, C.; Mantica, G.; Dimasi, A.; Rasponi, M.; Santoleri, A.; Scavone, M.; Consolo, F.; Cattaneo, M.; Slepian, M.J.; Redaelli, A. The MICELI (MICrofluidic, ELectrical, Impedance): Prototyping a Point-of-Care Impedance Platelet Aggregometer. Int. J. Mol. Sci. 2020, 21, 1174.Rights
© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
As key cellular elements of hemostasis, platelets represent a primary target for thrombosis and bleeding management. Currently, therapeutic manipulations of platelet function (antithrombotic drugs) and count (platelet transfusion) are performed with limited or no real-time monitoring of the desired outcome at the point-of-care. To address the need, we have designed and fabricated an easy-to-use, accurate, and portable impedance aggregometer called "MICELI" (MICrofluidic, ELectrical, Impedance). It improves on current platelet aggregation technology by decreasing footprint, assay complexity, and time to obtain results. The current study aimed to optimize the MICELI protocol; validate sensitivity to aggregation agonists and key blood parameters, i.e., platelet count and hematocrit; and verify the MICELI operational performance as compared to commercial impedance aggregometry. We demonstrated that the MICELI aggregometer could detect platelet aggregation in 250 μL of whole blood or platelet-rich plasma, stimulated by ADP, TRAP-6, collagen, epinephrine, and calcium ionophore. Using hirudin as blood anticoagulant allowed higher aggregation values. Aggregation values obtained by the MICELI strongly correlated with platelet count and were not affected by hematocrit. The operational performance comparison of the MICELI and the Multiplate® Analyzer demonstrated strong correlation and similar interdonor distribution of aggregation values obtained between these devices. With the proven reliability of the data obtained by the MICELI aggregometer, it can be further translated into a point-of-care diagnostic device aimed at monitoring platelet function in order to guide pharmacological hemostasis management and platelet transfusions.Note
Open access journalISSN
1422-0067EISSN
1422-0067PubMed ID
32053940Version
Final published versionae974a485f413a2113503eed53cd6c53
10.3390/ijms21041174
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Except where otherwise noted, this item's license is described as © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
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