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Two techniques for the preparation of platelet concentrate (PC), the standard platelet-rich plasma (PRP) and buffy coat (BC) methods, were compared in nine paired studies with regard to platelet harvest, white cell (WBC) contamination, and PC quality after 5 days of 22°C storage. Platelet harvest using the BC method averaged approximately 56 percent of the whole blood level (6.2 × 1010/concentrate), which was less than the 76 percent achieved with the PRP-PC method (8.7 × 1010/concentrate). An additional 5 units collected into an experimental siphon bag for BC-PC processing showed improved platelet harvest (6.7 × 1010/concentrate, or approx. 70% of whole blood). WBCs remaining in the BC-PC averaged 0.19 × 108 per unit compared to 3.6 × 108 per unit for PRP-PC. Buffy coat processing produced red cell (RBC) units with 50 percent of the WBC contamination of conventionally prepared units (9.8 ± 6.2 × 108/unit vs. 18.9 ± 7.1 × 108/unit). The siphon bag further reduced WBC levels in the AS-3 RBC units (6.4 ± 3.7 × 108/unit). In vitro studies performed on Days 1 and 5 after collection showed no significant differences in platelet metabolic and biologic function or cell integrity. β-thromboglobulin and surface glycoprotein levels, indicators of platelet activation and membrane alteration, respectively, did not differ significantly in the PRP-PC and BC-PC; nor was lactate production higher in PRP-PC, despite the substantially higher WBC counts. Autologous in vivo platelet viability determinations were performed by using concurrent transfusion of 111In-labeled freshly drawn platelets and 51Cr-labeled stored platelets. Paired f test analysis of BC-PC versus PRP-PC indicated no significant differences in platelet recovery and survival after 5 days of 22°C storage in polyolefin containers. Therefore, these studies confirm the equivalence of PC quality, comparable platelet harvest with the siphon bag, and decreased WBC contamination with the BC method.