Why the study?
Platelet size is a determinant of platelet function, motivating the development of a rapid and sensitive microfluidic method to determine platelet apparent size and evaluate platelet function nondestructively.
S-MDC is a rapid, label-free, and nondestructive technique for evaluating platelet function and monitoring antiplatelet drugs.
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Enables rapid label-free platelet sizing under physiological shear; leaves open clinical utility for function assessment pending validation.
Platelet size is a determinant of platelet function. Here, a new microfluidic deterministic cytometry packed with S -shaped micropillars ( S -MDC) was developed to rapidly and sensitively determine the apparent size ( D app ) of platelets, which was used to evaluate platelet function. The platelet D app in the diluted whole blood was rapidly and label-freely measured by S -MDC within 2 min under shear rates (0.4 mm/s) that mimicked physiological conditions. The level of CD62p on platelets scarcely changed before and after platelets went through the whole S -MDC, indicating that the platelet function was nondestructive. Notably, the human platelet D app determined before and after thrombin addition by S -MDC was highly coincident with the levels of CD62p on the platelet surface by flow cytometry ( r = 0.819), revealing that the human platelet D app was available to assess the platelet activation state. In addition, the results of the rat platelet D app were consistent with myocardial injury of rats with myocardial ischemia before and after treatment with antiplatelet agents, suggesting that rat platelet D app can be used to reflect myocardial injury in vivo outcomes. These findings reveal that S -MDC is a promising technique for screening tests for a bleeding disorder, in addition to monitoring antiplatelet drugs.
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Chen et al. (2023) studied this question.
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