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Bone healing and bio-engineered bone grafts:
 
One of the highest concentrations of TGF in the body is found within blood platelets. The TGF is a so-called "super family" of growth factors containing specific Bone Morph genetic Proteins (BMP). When TGF is released by platelet degranulation, they represent a growth factor mechanism that not only initiate bone regeneration, but also can sustain long-term healing.
With plasma sequestration the patients' platelets become concentrated, and therefore increase the concentration of these growth factors (TGF) in the graft manifold, thereby improving the likelihood of more successful and faster healing of the grafts and tissue.
Currently, when bone is needed to restore or reconstruct an area where there is a bony deficit or bone growth is desired (spinal fusions), grafting procedures are utilized with several different materials. The "gold standard" is still considered to be bone taken from the patient being treated (an autogenous bone graft). However, associated with the harvesting of autogenous bone might be the disadvantage of a second surgical site, with its attendant morbidities (pain, interference with function, risk of infection, etc.), and a limited amount of tissue available. In an attempt to decrease the morbidity associated with harvesting bone from the patient, substitute materials could be considered, either as the sole material, or in combination with autogenous bone, to decrease the amount of bone that must be harvested.
Bone regeneration may occur in several ways as a result of bone grafting:
The first is by osteogenesis, which occurs when autogenous bone is used. During osteogenesis, bone-forming cells and growth factors, derived from living cells that survive the transfer of the bone graft itself, occurs directly from bone.
The second is by osteo-induction. Osteo-induction occurs when a bone graft material is used which induces cells from the surrounding host tissues to invade the graft to form bone. The graft material recruits from the surrounding bed of messenchymal-type cells, which then differentiate into bone-forming cells. Osteo-induction is mediated by graft-derived factors; chemicals (growth factors) in the graft material which induce or influence the differentiation of these messenchymal cells into bone-forming cells. It is believed that demineralized bone (allografts) are osteo-inductive as a result of growth factors in the graft becoming exposed by the demineralization process. These growth factors then interact with, and stimulate messenchymal-type, cells to form bone.
The third way is by a process osteo-conduction. With osteo-conduction, the graft material just acts as a trellis, or scaffold, on which new bone, derived from the host tissue, can be formed. The graft material allows for the in growth of new host bone from the recipient bed into the structure of the graft, but nothing more. Most mineralized bone allografts are osteo-conductive; however, if growth factors are added to these osteo-conductive grafts, they may become osteo-indictive as well.
  The successful healing of a bone graft is dependent upon:
  The biological activity of the living cells in the graft itself (if any), and in the surrounding host tissue (osteoblasts; fibroblasts; messenchymal-type cells).
  The presence of signaling molecules (growth factors) in the graft, which activate surrounding host tissues to induce an appropriate bone-forming response.
  The ability of the graft to act as a scaffold and support the ingrowth of host tissue.
    When mixed with the graft material, whether autogenous bone, allograft material, or even xenografts, or a combination of these, the PRP will provide high concentrations of these growth factors, which will enhance the healing and quality of the grafted bone.