Background: Platelet transfusions are increasing with advances in medical care. Based on FDA criteria, platelet units are assessed by measures; however, it is not known how platelet processing and storage duration affect function . To address this, we developed a novel platelet transfusion model that meets FDA criteria adapted to mice, and transfused fresh and stored platelets are detected in clots .

Study Design And Methods: Platelet units stored in mouse plasma were prepared using a modified platelet rich plasma collection protocol. Characteristics of fresh and stored units, including pH, cell count, measures of activity, including activation and aggregation, and post-transfusion recovery (PTR), were determined. Lastly, a tail transection assay was conducted using mice transfused with fresh or stored units, and transfused platelets were identified by confocal imaging.

Results: Platelet units had acceptable platelet and white cell counts and were negative for bacterial contamination. Fresh and 1-day stored units had acceptable pH; the platelets were activatable by thrombin and ADP, aggregable with thrombin, had acceptable PTR, and were present in clots of recipients after tail transection. In contrast, 2-day stored units had clinically unacceptable quality.

Discussion: We developed mouse platelets for transfusion analogous to human platelet units using a modified platelet rich plasma collection protocol with maximum storage of 1 day for an "old" unit. This provides a powerful tool to test how process modifications and storage conditions affect transfused platelet function .

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10680660PMC
http://dx.doi.org/10.1101/2023.11.10.566577DOI Listing

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