The most widely used biomaterials are calcium-phosphate ceramics, which usually combine hydroxyapatite and tricalcium phosphate as granules or, more rarely, sticks, and exhibit interconnected pores each measuring 100–400 μm. These biomaterials promote the adhesion, proliferation, and osteoblastic differentiation of MSCs, as well as the production of the collagen matrix

Talazoparib mouse that subsequently undergoes mineralization. Collagen sponges and biodegradable polymers can also be used. The biomaterials must be absorbable, at a variable rate depending on their anticipated biomechanical role, and must allow the ingrowth of newly formed blood vessels from the neighboring tissues. Good quality vascularization of the tissue in contact with the implant is crucial. Although most of the available synthetic bone substitutes possess some of the positive

properties of autograft (particularly, osteoconductive capabilities and occasionally, osteoinductive properties), none has all the benefits of one’s own bone yet (osteogenic properties). Basically and PD-166866 molecular weight besides bone autografting, which is the only truly osteogenic material, orthobiological solutions today available to surgeons include osteoconductive and osteoinductive products, such as different preparations of bone allograft (fresh-frozen or dried by lyophilization, warranting osteoconduction), different synthetic substitutes (with variable properties but particularly osteoconductive), and synthetic

pharmaceuticals with osteoinductive properties (such as bone morphogenetic proteins, BMPs). Available evidence confirms the outcome of fractures and non-unions treated by surgical techniques augmented by autograft [55] and by BMPs [47]; thus this information may be compared to efficacy ID-8 studies about other solutions. An alternative strategy to accelerate bone healing includes the use of degradable biomaterials in combination with osteogenic factors. Besides the already mentioned growth factors, emerging anabolic osteogenic factors are under scrutiny. This applies not only to PTH but also to PTHrP whose C-terminal 107–111 domain (also known as osteostatin) exhibits osteogenic features in vitro, and stimulates bone formation in vivo [56], [57], [58], [59] and [60]. PTHrP also conferred both osteogenic and angiogenic preclinical features when coating Si-based ceramics both in vitro and in vivo [61] and [62]. But besides bone grafts, substitutes and their augmentation with growth factors and anabolic strategies, cell therapies have been proposed to evolve towards new osteoinductive and osteogenic solutions that could safely and efficaciously compete with currently available standards. In view of these limitations and the increasing number of bone grafting procedures, surgeons are looking for alternatives with added value compared to osteoconductive substitutes, such as cell therapy and tissue engineering [63].