Table of Contents
ISRN Hematology
Volume 2014, Article ID 176060, 8 pages
http://dx.doi.org/10.1155/2014/176060
Research Article

Relevant Aspects of Centrifugation Step in the Preparation of Platelet-Rich Plasma

1Department of Engineering of Materials and Bioprocesses, School of Chemical Engineering, University of Campinas, 13083-852 Campinas, SP, Brazil
2Research Institute of Sports Medicine, Orthopedics and Regeneration, iMOR, 38050-400 Uberaba, MG, Brazil
3Department of Orthopedics and Traumatology, Faculty of Medical Sciences, University of Campinas, 13083-887 Campinas, SP, Brazil
4Haematology and Hemotherapy Center, Umbilical Cord Blood Bank, University of Campinas, 13083-970 Campinas, SP, Brazil

Received 6 January 2014; Accepted 25 February 2014; Published 25 March 2014

Academic Editors: R. M. Camire, D. Del Principe, A. Kasirer-Friede, B. Olas, J. A. Rosado, and M. Torti

Copyright © 2014 Amanda G. M. Perez et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Introduction. Platelet-Rich Plasma (PRP) is rich in growth factors, playing important role in tissue healing. The wide variation of reported protocols for preparation of PRP leads to variable compositions, which induce different biological responses and prevent results comparison. This study aims to highlight relevant aspects of the centrifugation step to obtain reproducible results and overall quality. Material and Methods. Samples of blood were collected from 20 healthy donors that have signed free informed consent. Two centrifugation steps (spins) were analyzed for the influence of centrifugal acceleration, time, processed volume, and platelet gradient. The Pure Platelet-Rich Plasma (P-PRP) was characterized as platelet concentration, integrity, and viability (sP-selectin measurement). Results. Lower centrifugal accelerations favour platelet separation. The processing of 3.5 mL of blood at 100 ×g for 10 min (1st spin), 400 ×g for 10 min (2nd spin), withdrawing 2/3 of remnant plasma, promoted high platelet recovery (70–80%) and concentration (5x) maintaining platelet integrity and viability. The recovery of platelets was reduced for a larger WB volume (8.5 mL) processed. Conclusion. Centrifugal acceleration, time, WB processed volume, and minimization of the platelet gradient before sampling are relevant aspects to ensure reproducible compositions within the autologous nature of PRP.