Optimizing Platelet-Rich Plasma: Spin Time and Sample Source

Author:

Harrison Theodore E.1ORCID,Bowler Jannice2,Cheng Chin-I3ORCID,Reeves Kenneth Dean4ORCID

Affiliation:

1. Independent Researcher, Victoria, BC V8L 5K1, Canada

2. Independent Researcher, Victoria, BC V9E 1J5, Canada

3. Department of Statistics, Actuarial and Data Science, Central Michigan University, Mt. Pleasant, MI 48859, USA

4. Independent Researcher, Roeland Park, KS 66205, USA

Abstract

The buff-colored layer separating the plasma from red blood cells (RBCs) in centrifuged blood was named the “buffy coat” in the late 19th century. The division of platelets (PLTs) and leukocytes (WBCs) between the buffy coat, plasma, and RBC layers in centrifuged blood has not been described before. In this study, we centrifuged 8.5 mL anticoagulated blood samples at 1000× g for 1, 2, 3, 5, 10, and 20 min. We then divided each sample into ten layers and analyzed each layer for cellular composition and mean platelet volume (MPV). Our results show that even after 20 min of centrifugation, about 15% of platelets remain in the plasma layers and 65% in the RBC layers. We found that the platelet count achieved from aspiration of 1 mL volume was optimal, with aspiration beginning 1/2 mL below the buffy coat and extending 1/2 mL above the buffy coat rather than beginning at the buffy coat itself and aspirating only plasma. Using this method of aspiration, we found that the total platelet count means reached a maximum in the 1 mL around the buffy coat after only 5 min of centrifugation.

Publisher

MDPI AG

Subject

Bioengineering

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