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Relevant aspects of centrifugation step in the preparation of platelet-rich plasma.
Perez, Amanda G M; Lana, José Fábio S D; Rodrigues, Ana Amélia; Luzo, Angela Cristina M; Belangero, William D; Santana, Maria Helena A.
Afiliação
  • Perez AG; Department of Engineering of Materials and Bioprocesses, School of Chemical Engineering, University of Campinas, 13083-852 Campinas, SP, Brazil.
  • Lana JF; Research Institute of Sports Medicine, Orthopedics and Regeneration, iMOR, 38050-400 Uberaba, MG, Brazil.
  • Rodrigues AA; Department of Orthopedics and Traumatology, Faculty of Medical Sciences, University of Campinas, 13083-887 Campinas, SP, Brazil.
  • Luzo AC; Haematology and Hemotherapy Center, Umbilical Cord Blood Bank, University of Campinas, 13083-970 Campinas, SP, Brazil.
  • Belangero WD; Department of Orthopedics and Traumatology, Faculty of Medical Sciences, University of Campinas, 13083-887 Campinas, SP, Brazil.
  • Santana MH; Department of Engineering of Materials and Bioprocesses, School of Chemical Engineering, University of Campinas, 13083-852 Campinas, SP, Brazil.
ISRN Hematol ; 2014: 176060, 2014.
Article em En | MEDLINE | ID: mdl-25006472
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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ISRN Hematol Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ISRN Hematol Ano de publicação: 2014 Tipo de documento: Article