Publication | Open Access
From Platelet-Rich Plasma to Advanced Platelet-Rich Fibrin: Biological Achievements and Clinical Advances in Modern Surgery
120
Citations
33
References
2019
Year
Platelet-rich FibrinTissue EngineeringEngineeringCell AdhesionImmunologySurgeryBiomedical EngineeringSkin RegenerationRegenerative MedicineThrombosisHematologyPlatelet ConcentratesVascular SurgeryRegenerative BiomaterialsMatrix BiologyAdvanced Platelet-rich FibrinTissue RepairPlatelet BiologyVascular Tissue EngineeringModern SurgeryFibrinolysisWound InfectionFunctional Tissue EngineeringCell BiologyPlatelet-derived Growth FactorTissue RegenerationThrombopoiesisBlood PlateletHemostasisWound HealingPlatelet-rich PlasmaMedicineBiomaterialsExtracellular Matrix
Platelet concentrates have evolved from first‑generation platelet‑rich plasma to second‑generation leukocyte‑rich fibrin products such as L‑PRF and A‑PRF, which provide a flexible, physiologic fibrin matrix rich in leukocytes and growth factors that enable sustained release of angiogenic, osteogenic, and antimicrobial signals for tissue regeneration. The authors propose expanding the use of these platelet‑rich fibrin products to tissue regeneration and grafting, diabetic ulcer and skin necrosis treatment, plastic surgery, and musculoskeletal lesion repair. L‑PRF and A‑PRF have already been applied successfully in implantology, periodontology, and maxillofacial surgery.
In the past 20 years, the platelet concentrates have evolved from first-generation products, i.e., platelet-rich plasma (PRP) and plasma rich in growth factors to the second-generation products such as leukocyte-platelet-rich fibrin (L-PRF) and advanced platelet-rich fibrin (A-PRF). These autologous products with a higher leukocyte inclusion and flexible fibrin mesh act as a scaffold to increase cellular migration in the angiogenic, osteogenic, and antimicrobial potential of these biomaterials in tissue regeneration. In the second-generation platelet concentrates, the protocols are easier, cheaper, and faster with an entire physiological fibrin matrix, resulting in a tridimensional mesh, not as rigid as one of the first generations. This allows the slow release of molecules over a longer period of time and triggers the healing and regenerative process at the site of injury. The potential of A-PRF to mimic the physiology and immunology of wound healing is also due to the high concentration of growth factors released as follows: vascular endothelial growth factor, platelet-derived growth factor, transforming growth factor-β, and anti-inflammatory cytokines that stimulate tissue cicatrization, vessels formation, and bone cell proliferation and differentiation. Furthermore, the number of neutrophils and monocytes/macrophages is higher releasing important chemotactic molecules such as chemokine ligand-5 and eotaxin. Thus, L-PRF and A-PRF have been used, especially in implantology, periodontology, and maxillofacial surgery. Future clinical applications include tissue regeneration/grafts, ulcers/skin necrosis in the diabetic patient and others, plastic surgery, and even musculoskeletal lesions.
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