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BackgroundPlatelet-rich plasma (PRP) has been advocated as a way to introduce increasedconcentrations of growth factors and other bioactive molecules to injured tissuesin an attempt to optimize the local healing environment. Many methods for PRPpreparation have been introduced. Despite variations in the volume of whole bloodtaken and the efficacy of the platelet concentration, the main objective of PRP preparation is to obtain sufficient platelet concentration in the finally processed autologousplasma. We have been making our own internal primitive PRP preparation, which issafe and aseptic, using simple tubes and a centrifugal separator at the outpatient department base. MethodsTwenty cc of whole blood was collected and 10 cc of blood was added to eachof two bottles, followed by addition of 1.5 cc adenosine-citrate-dextrose-acid solutionto each bottle. Then, centrifugal separation was performed at 4,000 RPM for 15 minutes. Then, the buffy coat layer was aspirated using a 10 cc syringe equipped with a spinal needle. Platelet activation was initiated by addition of CaCl2 and botropase. Results We were successful in attaining PRP, which was three folds and six folds concentrated compared with the initial platelet count of whole blood . ConclusionsOur protocol is economical and only requires a few simple procedures for preparation of PRP. We expect the protocol to be applied to clinical trials without significantcost of time and money.

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