Resumo:
Leukocyte and Platelet-Rich Fibrin (L-PRF) has been used as a regulator of the
healing process because it is an important source of cytokines and growth
factors. L-PRF is an autologous product from the centrifugation of blood samples.
The success of the technique is intrinsically related to the blood processing
protocols collected and the type of used centrifuge. This study aimed to evaluate,
comparatively macro and microscopically using the hematoxylin/eosin (H/E)
technique, the formation of the L-PRF membrane/clot in two different models of
centrifuges, the Intra-Spin - Intra-Lock and the Montserrat centrifuge. Four blood
samples were used from 8 healthy volunteers who underwent rehabilitation
surgery with dental implants. Two types of centrifuge with different centrifugation
protocols were used. In group 1 of the Montserrat centrifuge, 400gm of centrifugal
force at 10 minutes, 27ºC and 2700 rpm were used, while in group 2 of the IntraSpin Intra-Lock centrifuge, 400g of centrifugal force at 12 minutes, 27ºC and
2700 rpm were used. The blood was collected quickly and randomly distributed
in the centrifuges. At the end, 32 clot/membrane L-PRFs were obtained. Then,
the pieces were registered and sent for macroscopic analysis, of the variables of
weights and sizes of clots/membranes of L-PRFs and weight of the
supernatant/clot of red blood cells remaining in the tubes. Then, the specimens
were processed for routine histological technique (H/E). Each slide was divided
into three areas of equal size: Proximal (Head and Face), Center (Body) and
Distal (Tail), andw was analyzed semiquantitatively for the presence of
leukocytes. The results demonstrate that the membranes produced in the IntraSpin - Intra-Lock centrifuge present leukocytes in, at least, 2 areas
simultaneously (62.5%) (p = 0.003). Regarding leukocyte intensity (p = 0.012),
leukocyte percentage (p = 0.037), leukocyte distribution (p = 0.005) and leukocyte
location (p = 0.037), both were statistically higher in the central areas of the LPRFs produced in the Intra-Spin - Intra-Lock centrifuge when compared to the
central areas of those produced in Montserrat. With regard to macroscopic
characteristics, no statistically relevant differences were found in any of the LPRFs produced by the two centrifuges. It is suggested that the different protocols
influence the presence and distribution of leukocytes between the membranes of
L-PRFs. New studies must be carried out to expand this characterization.