TY - JOUR
T1 - Plasma rich in growth factors (PRGF) for the promotion of bone cell proliferation and tissue regeneration
AU - BRUCOLI, Matteo
AU - SONZINI, Roberta
AU - BOSETTI, Michela
AU - BOFFANO, PAOLO
AU - Benech, Arnaldo
N1 - Publisher Copyright:
© 2018, Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2018
Y1 - 2018
N2 - Objectives: Over the past few years, studies about growth factors have been increasingly developed and the knowledge of their role in stimulating cell proliferation and differentiation used for therapeutic purposes. This study aims to compare a platelets concentrate, the plasma rich in growth factors (PRGF) to a control, consisting of cellulose membranes, to evaluate in vitro the cellular adhesion and migration of human osteoblasts (hOb) and understand if the use of platelets concentrates could be an advantage in view of bone tissue regeneration. Study design: Twenty-seven human donors provided 27 blood samples used to make 54 samples: 27 for PRGF and 27 for the control group. PRGFs and controls were incubated for 48 h in sterility in 1 ml of culture with 105 hOb and hOb in the scaffolds were then quantified. Results: In PRGF samples, hObs were more numerous than in controls. (T = 6.6964, p < 0.0001). Conclusions: Human osteoblasts are driven to colonize PRGFs with a greater efficacy than negative controls, probably due to the presence of chemokines and growth factors in PRGFs.
AB - Objectives: Over the past few years, studies about growth factors have been increasingly developed and the knowledge of their role in stimulating cell proliferation and differentiation used for therapeutic purposes. This study aims to compare a platelets concentrate, the plasma rich in growth factors (PRGF) to a control, consisting of cellulose membranes, to evaluate in vitro the cellular adhesion and migration of human osteoblasts (hOb) and understand if the use of platelets concentrates could be an advantage in view of bone tissue regeneration. Study design: Twenty-seven human donors provided 27 blood samples used to make 54 samples: 27 for PRGF and 27 for the control group. PRGFs and controls were incubated for 48 h in sterility in 1 ml of culture with 105 hOb and hOb in the scaffolds were then quantified. Results: In PRGF samples, hObs were more numerous than in controls. (T = 6.6964, p < 0.0001). Conclusions: Human osteoblasts are driven to colonize PRGFs with a greater efficacy than negative controls, probably due to the presence of chemokines and growth factors in PRGFs.
UR - https://iris.uniupo.it/handle/11579/98058
U2 - 10.1007/s10006-018-0712-z
DO - 10.1007/s10006-018-0712-z
M3 - Article
SN - 1865-1550
VL - 22
SP - 309
EP - 313
JO - Oral and Maxillofacial Surgery
JF - Oral and Maxillofacial Surgery
IS - 3
ER -