- Pure Platelet-Rich Plasma (P-PRP), such as cell separator PKP, vivostat PRF or Anitua's PRGF.
- Leucocyte-and Platelet-Rich Plasma (L-PRP), such as Curasan, Kegen, Plateltex, Smart PReP, PCCS, Magellan or GPS PRP.
- Pure Platelet Rich Fibrin (PRGF), such as Fibrinet and Leucocyte.
- Platelet-Rich Fibrin (L-PRF), such as Choukroun's PRF, T-PRF (Titanium PRF), I-PRF (Injectable PRF), A-PRF (Advance PRF) all these variants are due to either differences between centrifuge speed or use of titanium as a collection tube instead of normal glass tubes or vacuum blood collection tubes.
- Concentrated Growth Factors (CGF).
| Growth Factors | Primary functions |
| Epidermal growth factors (EGP) | Regulation of cell proliferation, differentiation, and survival. |
| Insulin like growth factors IGF | Key regulators of cell metabolism and growth Stimulates proliferation and differentiation functions in osteoblast |
| Platelet derived growth factor | Mitogen for connective tissue cells and other cell types. Enhance the synthesis of collagen and structural proteins |
| Transforming growth factors alpha beta | Regulation of cell proliferation, differentiation and apoptosis Induction of intimal thickening |
| Vascular endothelial growth factor | Regulation of angiogenesis |
- Epidermal Growth factors (EGP)
- Regulation of cell proliferation, differentiation and survival.
- Insulin like growth factors IGF
- Venous blood is drawn and mixed with anticoagulant to avoid platelet activation and degranulation.
- The first soft spin centrifugation separates blood in 3 distinct layers:
- The red blood corpuscles constitute 55% of total volume form the bottom layer of the tube.
- The acellular plasma layer is mainly made up of fibrinogen and low in platelets called as Platelet-Poor Plasma (PPP) and constitutes 40% of total volume forms a top layer of the tube.
- Between the 2, an intermediate layer is where platelets concentrations are largely increased. It constitutes only 5% of total volume called as buffy coat. It will compose the major part of the future PRP, but at this stage, it is non separable completely.
- A sterile syringe is used to aspirate PPP, PRP and some red blood corpuscles, the remaining content is transferred to another tube which is anticoagulant less.
- This second tube will then undergo another centrifugation, purported to be longer and faster than the first (‘‘hard spin’’). This makes it possible to concentrate platelets at the bottom of the tube and subsequently to obtain once again 3 distinct layers some residual red blood corpuscles trapped at the bottom of the tube and at the top acellular plasma (PPP) consists of 80% of total volume and between these two a buffy layer called PRP.
- It becomes easy to collect the PRP at this stage. Major part of the PPP is discarded by using a syringe, just leaving some serum to place the platelet concentrate in suspension. The unit is then gently shaken to obtain a ready-to-use PRP. Note that the red blood corpuscles trapped at the bottom of the tube are also suspended by this last operation, which explains the rosy aspect of the final PRP.
- PRP is then mixed with bovine thrombin and calcium chloride at the time of application, with the help of a mixing syringe. Gelling of platelet concentrate will then quickly occur: Fibrinogen is also concentrated during the PRP preparation and its polymerisation will constitute a fibrin matrix with particularly interesting homeostatic and adhesive properties.
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PRF preparation PRF protocol is very simple compared to PRP. Venous blood is drawn without anticoagulant in 10 ml tubes which centrifuged immediately at 3000 rpm (approximately 400 g) for 10 minutes. Care in handling of blood and quick action is required.
Properties of PRF