Platelet rich plasma (PRP) application is a successful fibrin membranes in such cases can prepare the wound catalyst in the healing process for wide varieties of for skin grafting earlier, reducing the time for total conditions. PRP therapy began gaining popularity in the healing. This results in improved quality of life and mid 1990s. Methods of harvesting and using platelet rich lower cost of care over other conventional therapies. plasma are becoming widely practiced in the fields of sports medicine, orthopedics, traumatology, general PRP Product to be used : surgery, dentistry, dermatology and cosmetology and Concentrated PRF preparations ( typically 7-10 times aesthetic medicine. concentration of platelets in fibrin clot) are used in these Main function is hemostasis by attaching to any breach conditions. Quantity required varies depending on area in vessel where platelets aggregate, activate and release of wound and PRF membranes can be prepared with the granules. Alpha granules contain clotting mediators such size of 60 mm discs. Depending on the area required as factor V, factor VIII, fibrinogen, fibronectin, platelet- number discs can be prepared. derived growth factors, and chemotactic agents. Delta granules, or dense bodies, contain ADP, calcium, serotonin, which are platelet-activating mediators. Material provided: Activated platelets release granules by exocytosis which contain more than sixty different biologically active 1. PRP-50 sterile anticoagulant Ampoule 5 ml. substances that are involved in processes of tissue 2. PRP activator 1 ml ampoule regeneration, angiogenesis, epithelialization, 3. PRP Test tubes 15 ml 3 nos Sterile proliferation and differentiation of osteoblasts, and in 4. PRP Transfer pipettes 3 ml 1 pair Sterile synthesis of collagen and extracellular matrix of 5. Sterile disposable 60 mm petri dishes connective tissue. (All material sterile for 3 years from manufacture) Use of PRP in Non-healing skin Ulcers : Other Material required: Any wound goes through stages of acute inflammation, increased mitotic activity and finally orderly repair. 1. Centrifuge 15 ml and/or 50 ml rotor with timer and RPM Meter. Chronic wounds can be those wounds failing to proceed 2. Incubator with digital control through an orderly and timely process produce anatomic and functional integrity. Practically, a chronic wound is 3. Test Tubes stand for 10 ml and 50 ml tubes the one which has failed to heal within 3 months. Procedure : Repeated trauma, foreign bodies, pressure necrosis, 1. Take 10 ml, 15 ml or 50 ml tube as per the need infection, ischemia and tissue hypoxia are few of the 2. Add 1.5 ml or 5 ml anticoaguland and collect reasons of non healing. Growth factors are crucial for 13.5 ml blood by using scalp vein set 18 No. timely wound healing. Platelets can fill the gap by directly to the anticoagulant added tubes. supplying growth factors. It is desirable to supply Depending on need additional number of tubes growth factors over extended time and this can be can be set-up. Discard remaining anticoagulant. achieved by delivering platelets in fibin matrix. 3. Cap the tubes tightly and Mix well by inversion Fibrin membranes are very useful for treating chronic several times. diabetic non healing ulcers, and pressure sores. Use of 4. Centrifuge for 15 min at 1500 RPM 5. Plasma rich in platelets will be separated. At 10. Apply appropriate dressing and leave the least 50% volume should be plasma on top and dressing for 5-7 days. there should not be any buffy coat on the RBC layer. If plasma is less, centrifugation needs to be increased and if buffy coat forms, centrifugation needs to be reduced. What to expect : 6. Transfer plasma to sterile petri dishes using The PRF membrane releases growth factors over next sterile pipette. Petri dishes should be kept one week and rapid growth of healthy granulation tissue horizontal on vibration free surface. is expected in 1-2 weeks. The Membrane application can 7. Add 0.5 ml activator for each 10 ml plasma in be repeated 1-2 times as required depending on the that proportion and mix gently. healing and suitability of grafting. 8. Cover the petri dish with its cover in incubator at 37C and allow to clot for 10-15 min. 9. Very thin clot membrane will form which then is applied to wound directly from the plate.
Please contact Dr. S K Hayatnagarkar, Cryobank Fertility Research Centre, Kamgar Chowk, N- 2, CIDCO Aurangabad Cell & Whatsapp: 9422725000, 9890900585