Platelet activation of platelet concentrates derived from buffy coat and apheresis methods

• Published in: Transfusion and apheresis science Vol. 44; no. 1; pp. 11 - 13
• Main Author: Ali, Soleimany Ferizhandy
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.02.2011
• Subjects: Adult; Annexin A5 - analysis; Annexin V; Blood Cell Count; Blood Component Removal - methods; Blood Donors; Blood Platelets - chemistry; Blood Platelets - physiology; Blood Preservation - methods; Buffy coat; Cell Separation; Cell Size; Centrifugation - methods; Health technology assessment; Hematology, Oncology and Palliative Medicine; Humans; Hydrogen-Ion Concentration; PF4; Platelet Activation; Plateletpheresis; Plateletpheresis - instrumentation; Plateletpheresis - methods; Time Factors; Annexin V; Buffy coat; Plateletpheresis; PF4
• ISSN: 1473-0502; 1878-1683
• DOI: 10.1016/j.transci.2010.12.002

Abstract Preparation for storage may cause platelet activation. The quality of platelet concentrates plays an important role in transfusion therapy. Platelet concentrates are produced by different centrifugation methods; buffy coat (buffy coat-derived platelet concentrates-BC) and plateletpheresis (apheresis-derived platelet concentrates-APC). Their quality was assessed using the following parameters: platelet, WBC and RBC counts pH, volume, platelet factor 4 (PF4) and Annexin V. The present paper compares the quality of both platelet preparations in vitro. In this experimental study, 30 platelet concentrates were harvested with the Haemonetics MCS plus and 30 units via the buffy coat (BC) method. The percentages of Annexin V expression, PF4 levels, platelet, WBC and RBC counts, pH and volume were measure immediately after collection and after 3 days of storage. During storage for up to 3 days, BC units displayed, no significant pH or RBC, difference in comparison with apheresis preparations ( p > 0.05). During storage for up to 3 days, BC units displayed a significant increase in the PF4 and Annexin V expression, compared to the apheresis preparations on day three ( p < 0.05). The kinetics of PF4 and Annexin V levels are influenced by the method used to prepare platelets for storage. The different levels of PF4 and Annexin V in BCs and APCs clearly demonstrates a progressive activation of BC platelets exceeding that of APC. However, in vivo studies should be performed to confirm these findings.