Summary

Caratterizzazione di leucociti-piastrine Rich fibrina, un biomateriale Novel

Published: September 29, 2015
doi:

Summary

Leucocyte-Platelet Rich Fibrin (L-PRF) represents an FDA cleared preparation of autologous platelet concentrates that possesses unique fibrin architecture, enriched platelets and abundant growth factors. Here, we present a protocol for chair-side generation of L-PRF as well as evaluate its mechanical properties including uniaxial testing and suture retention strength testing.

Abstract

Autologous platelet concentrates represent promising innovative tools in the field of regenerative medicine and have been extensively used in oral surgery. Unlike platelet rich plasma (PRP) that is a gel or a suspension, Leukocyte-Platelet Rich Fibrin (L-PRF) is a solid 3D fibrin membrane generated chair-side from whole blood containing no anti-coagulant. The membrane has a dense three dimensional fibrin matrix with enriched platelets and abundant growth factors. L-PRF is a popular adjunct in surgeries because of its superior handling characteristics as well as its suturability to the wound bed. The goal of the study is to demonstrate generation as well as provide detailed characterization of relevant properties of L-PRF that underlie its clinical success.

Introduction

The use of blood and blood-derived products to seal wounds and improve healing in different clinical situations started with fibrin glues, which are mainly fibrinogen concentrates. Addition of platelets to fibrin glue not only improved their strength but also promoted neoangiogenesis and regeneration. These benefits are attributed to the release of a variety of peptide growth factors from the alpha-granules of platelets upon activation1. Platelet concentrates (PC) were seen as a practical way to deliver growth factors2 and its use was driven by commercial interests rather than research characterization3. In fact, PCs are difficult to characterize unlike homogenous and defined pharmacological preparations, they are a potpourri of signaling molecules and blood cells (platelet and leukocytes) entrapped within a fibrin matrix. Different commercial and proprietary preparations yield a variety of PC that are different in cellular composition, growth factor recovery and kinetics of release4.

It is important to realize that in most oral surgeries, platelet-rich plasma (PRP) preparations are used as a gel in open surgical wounds and not as platelet suspensions. In these situations, the gelation is induced by the addition of thrombin, calcium chloride, batroxobin or other agents and directly placed in the site of injury5. Due to rapid activation, fibrinogen polymerization is often incomplete and results in friable fibrin gels with very little mechanical strength. In addition, injectable PRP gels undergo rapid fibrinolysis6,7.

In contrast, the processes of blood coagulation (fibrinogen polymerization), platelet enrichment and activation occur simultaneously in the preparation of L-PRF8. The coagulation cascade is triggered when whole blood contacts the walls of a dry glass tube and continues throughout the centrifugation process. This results in the formation of a mechanically-strong blood clot (L-PRF) that can be surgically handled and used.

Even though L-PRF has been investigated in terms of optimal methods of preparation, growth factor release and cell distribution9-11, detailed mechanical characterization of these membranes are lacking. This is significant gap in knowledge, given the popularity of these membranes in clinical practice as well as its potential to be used as a biomaterial. Current study focusses on the protocol for deriving L-PRF as well as methods that can be employed to study its mechanical properties. This data is intended to serve as baseline for ongoing studies investigating the viscoelastic properties of this interesting natural biomaterial.

Protocol

Tutte le procedure di sangue disegno devono essere effettuate da professionisti abilitati e certificati. L'utilizzo di soggetti umani per la ricerca riguarda l'approvazione del Institutional Review Board o altra autorità. Precauzioni particolari per quanto riguarda il consenso informato e che proteggono l'identificazione dei partecipanti devono essere seguite. Tutti gli esperimenti elencati in questo protocollo riguardano la manipolazione del sangue umano e / o di prodotti ematici e dispositivi di protezion…

Representative Results

L'immagine microscopio elettronico a scansione del coagulo L-PRF in diverse sezioni (superiore, centrale e inferiore) strato è illustrato nella figura 2. Come si può vedere, la parte superiore è costituita prevalentemente da rete di fibrina senza cellule. Lo strato intermedio è arricchito con piastrine con evidenza della loro attivazione e degranulazione. Lo strato inferiore è un misto di leucociti e globuli rossi intrappolate all'interno di una matrice di fibrina. <p class="jove_conten…

Discussion

Concentrati piastrinici autologhi sono promettenti nel campo della medicina rigenerativa 18 per l'abbondanza di fattori di crescita. Tuttavia, questi preparati spesso mancavano di una struttura definita che rende molto difficile la manipolazione chirurgica. Molte volte, le sospensioni e gel non si mantengono efficacemente nel sito di consegna, con conseguente esiti imprevedibili. L-PRF rappresenta un enorme progresso nell'evoluzione di concentrati piastrinici in quanto è essenzialmente una membrana d…

Divulgazioni

The authors have nothing to disclose.

Acknowledgements

The project was supported by CTSA (UL1TR000058) from the National Center for Advancing Translational Sciences) and the CCTR Endowment Fund of Virginia Commonwealth University. The contents are solely the responsibility of the authors and do not necessarily represent official views of the National Center for Advancing Translational Sciences or the National Institutes of Health.

Materials

Needle 19G BD 305186
Needle Disposal Container Fisherbrand 14-827-122
Red-Topped Glass Collection Tube BD 8020129
Gauze Pads Tyco 5750
Bandage Johnson & Johnson 5005989
Surshield Terumo SV*S19BL Safety winged infusion set
Blood Collection Assembly BD 303380
Tourniquets BD 367203
Brand Luer Adapter Vacutainer L42179
Intra-Spin System  Intra-Lock International ISS110 Centrifuge and Xpression L-PRF FabricationKit 
Pipettes (Serological & Micro) Corning
Scalpel Exelint 29552
MTS Bionix 200 MTS Systems Corporation Material testing systems
MTS Test Works 4 MTS Systems Corporation
Whatman Filter Paper Whatman 1004 070
SS Orthodontic ligature wire Patterson Dental 628-4228
200 Proof Ethanol Koptec V1001
Hexamethyldisilazane (HMDS) Aldrich 440191
Aluminium Mounting Stubs Ted Pella 16324
Double Sided Carbon Tape PELCO Tabs 16084-1
Scanning Electron Microscope JEOL LV 5610
Trypsin HyClone SH30042.01
Cell Culture Incubator Thermo Fisher Scientific Inc 51026282
Antibiotic-Antimicotic Gibco 15240-062
Genipin Wako 078-03021
Cell Culture Media Gibco 12000-022 Minimum Essential Medium-Alpha
MTS Reagent Promega G1118
PMS Reagent Sigma P9625
Spectrophotometer BioTek Epoch Spectrophotometer
10mm Glass Cloning Rings Corning 3166-10
T-75 Flask Corning 430641
DPBS Corning 55-031-PB
Ninhydrin 98% Aldrich 454044
24 Well Plate Corning 3987
Biopsy Punch Acu Punch P1025
Digital Micrometer Pittsburgh 68305
Glutaraldehyde Sigma G6257
12 Well Plate Corning 3336
96 Well Plate Corning 3596

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Citazione di questo articolo
Madurantakam, P., Yoganarasimha, S., Hasan, F. K. Characterization of Leukocyte-platelet Rich Fibrin, A Novel Biomaterial. J. Vis. Exp. (103), e53221, doi:10.3791/53221 (2015).

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