Patents
Literature
Hiro is an intelligent assistant for R&D personnel, combined with Patent DNA, to facilitate innovative research.
Hiro

33 results about "Platelet-rich fibrin" patented technology

Platelet-rich fibrin (PRF) or leucocyte- and platelet-rich fibrin (L-PRF) is a second-generation PRP where autologous platelets and leucocytes are present in a complex fibrin matrix to accelerate the healing of soft and hard tissue and is used as a tissue-engineering scaffold for endodontics. To obtain PRF, required quantity of blood is drawn quickly into test tubes without an anticoagulant and centrifuged immediately. Blood can be centrifuged using a tabletop centrifuge for at least 10 min at 3000 revolution per minute. The resultant product consists of the following three layers; topmost layer consisting of platelet poor plasma, PRF clot in the middle, and red blood cells at the bottom. PRF is available as a fibrin clot. PRF clot can be removed from the test tube using a sterile tweezer-like instrument. After lifting, the RBC layer attached to the PRF clot can be carefully removed using a sterilized scissor. Platelet activation in response to tissue damage occurs during the process of making PRF release several biologically active proteins including; platelet alpha granules, platelet‑derived growth factor (PGDF), transforming growth factors‑β (TGF‑β), vascular endothelial growth factor (VEGF), and epidermal growth factor. Actually the platelets and leukocyte cytokines are important part in role play of this biomaterial, but the fibrin matrix supporting them is very helpful in constituting the determining elements responsible for real therapeutic potential of PRF. Cytokines are immediately used and destroyed in a healing wound. The harmony between cytokines and their supporting fibrin matrix has much more unique importance than any other platelet derivatives.

Implant material with PRF precursor liquid solidified into gel mask

The invention relates to an implant material with a PRF (Platelet-Rich Fibrin) precursor liquid solidified into a gel mask, and belongs to the field of the implant materials for mucocutaneous operations. The implant material provided by the invention is characterized in that a non-anti-coagulation blood sample is employed, and centrifuged by a centrifuge with centrifugal force ranging from 130 to 460g, the upper total yellow liquid is put into standing at the room temperature for 30-40 minutes, and then the total yellow liquid is pressed into a mask for clinical application by a metal pressing plate. The implant material provided by the invention is high in yield, and can be naturally formed into gel without adding thrombin and calcium ions; as a result, the use risk of biochemical preparations is avoided; the operation of the implant material is simple; the PRF gel product is thick in fibrous protein filaments, good in elasticity and tenacity, strong in tension, high in hardness, slow in degradation, and not easy to break by tearing; almost no damage is caused in the preparation process of hemameba, blood platelet and shed particles of the two; and after being implanted in vivo, the implant material slowly releases various growth factors and anti-inflammatory cytokines to promote wound healing.
Owner:PEKING UNIV SCHOOL OF STOMATOLOGY

An implant material that solidifies prf precursor fluid into a gel film

The invention relates to an implant material with a PRF (Platelet-Rich Fibrin) precursor liquid solidified into a gel mask, and belongs to the field of the implant materials for mucocutaneous operations. The implant material provided by the invention is characterized in that a non-anti-coagulation blood sample is employed, and centrifuged by a centrifuge with centrifugal force ranging from 130 to 460g, the upper total yellow liquid is put into standing at the room temperature for 30-40 minutes, and then the total yellow liquid is pressed into a mask for clinical application by a metal pressing plate. The implant material provided by the invention is high in yield, and can be naturally formed into gel without adding thrombin and calcium ions; as a result, the use risk of biochemical preparations is avoided; the operation of the implant material is simple; the PRF gel product is thick in fibrous protein filaments, good in elasticity and tenacity, strong in tension, high in hardness, slow in degradation, and not easy to break by tearing; almost no damage is caused in the preparation process of hemameba, blood platelet and shed particles of the two; and after being implanted in vivo, the implant material slowly releases various growth factors and anti-inflammatory cytokines to promote wound healing.
Owner:PEKING UNIV SCHOOL OF STOMATOLOGY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products