Name: PRP as a New Approach to Prevent Infection: Preparation and In vitro Antimicrobial Properties of PRP (Video) | JoVE Journal
Uploaded: 2013-04-09T12:00:00.000+00:00
Duration: 6 min 36 s
Description: Learn to prepare platelet-rich plasma and evaluate its antimicrobial properties against bacteria in vitro. This method demonstrates significant CFU reduction and supports infection prevention strategies.

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The authors thank Therwa Hamza, John E. Tidwell, Nina Clovis, and Suzanne Smith for experimental assistance and Suzanne Smith for proofreading. The authors also thank John Thomas, PhD for providing the bacterial clinical isolates and John B. Barnett, PhD for his support and the use of the biological safety lab at the Department of Microbiology, Immunology and Cell Biology at West Virginia University. The authors acknowledge financial support from the Osteosynthesis and Trauma Care Foundation and National Science Foundation (#1003907). Microscope experiments and image analysis were also performed in the West Virginia University Imaging Facility, which is supported in part by the Mary Babb Randolph Cancer Center and NIH grant P20 RR016440.
Animal use for blood draws were approved by the West Virginia University Institutional Animal Care and Use Committee. All experiments were executed in compliance with all relevant guidelines, regulations, and regulatory agencies.

1. Preparation and Activation of PRP
1.1 Blood draw
<ol>
	<li>Anesthetize rabbit by inhalation of isoflurane (2% in O2 for induction and 1% for maintenance).</li>
	<li>Draw 2 ml 0.129 M tri-sodium citrate (an anticoagulent solution) into a 20 ml syringe. The tri-sodium citrate solution is prepared by dissolving 1.897 g tri-sodium citrate in 50 ml distilled H2O and filtering with a 0.22 &mu;m sterile filter.</li>
	<li>Sterilize the rabbit ear using 70% ethanol.</li>
	<li>Draw blood (e.g. 5 ml) from the rabbit ear vein via a butterfly needle (25 G) connected to the syringe.</li>
	<li>Mix the blood with the tri-sodium citrate solution by gentle agitation. The volume ratio of blood and tri-sodium citrate solution is 9:1.</li>
</ol>
1.2 PRP preparation (Figure 1)
<ol>
	<li>Transfer the anticoagulated blood to a 50 ml plastic centrifuge tube. Take an aliquot of 10 &mu;l blood to determine the baseline platelet count using hemocytometry.</li>
	<li>Centrifuge the blood at 300 x g for 10 min at room temperature (RT) in a centrifuge with a swing-out rotor. Set the acceleration and brake velocity to low (Figure 1).</li>
	<li>After centrifugation, the blood is separated into three layers. The bottom layer is mainly red blood cells, the middle layer (commonly referred to as the "buffy coat") is composed of concentrated platelets and leukocytes, and the top layer is mainly plasma, which is the liquid component of blood, and platelets (Figure 1). Carefully transport the centrifuge tube to a cell culture hood; do not disturb the layers. Transfer all of the plasma, buffy coat, and 2-3 mm thick red blood cell layer into a 15 ml plastic tube using a 1 ml plastic pipettor.</li>
	<li>Centrifuge the transferred sample a second time at 3,000 x g for 15 min at RT. The top layer (supernatant) is considered platelet poor plasma (PPP) and is transferred to a new tube.</li>
	<li>Obtain PRP by adjusting the platelet concentration in the remaining blood sample using PPP to obtain 2.0 x 106 platelets/&mu;l (determined by hemocytometry).</li>
</ol>
1.3 PRP activation
<ol>
	<li>Prepare PRP activation solution by dissolving 5,000 IU bovine thrombin with 5 ml 10% calcium chloride to the working concentration of 1,000 IU/ml.</li>
	<li>Add the activation solution to PRP and PPP, and mix the solution by repeatedly pipetting to form PRP- and PPP-gels. The volume ratio of the activation solution to PRP or PPP is 1:4.</li>
</ol>
2. In vitro Antimicrobial Test of PRP Using Kill Curve Assay (Figure 2)
<ol>
	<li>Using a sterile inoculating loop, add several colonies of S. aureus from its overnight plate culture into 5 ml of Mueller Hinton broth (MHB) in a plastic tube. Vortex briefly and then incubate the sample for 2 hr at 37 &deg;C. Next, the optical density of the bacterial media was determined using a spectrophotometer and adjusted to an optical density equal to ~1 x 108 CFU/ml based on the pre-determined standard curve.</li>
	<li>Make a 100x dilution using PBS to obtain 1 x 106 CFU/ml and place the inoculums on ice.</li>
	<li>Set up and label sterile, disposable 5 ml round-bottom polystyrene tubes, and prepare the following sample groups as indicated in Table 1 for a final volume of 2 ml in each tube.</li>
	<li>Add PRP, PPP, or PBS first to the polystyrene tubes, followed by the thrombin solution for activation (gel formation). Next, add MHB and then the S. aureus inoculums (1 x 106 CFU/ml) to obtain the final concentration of 1 x 105 CFU/ml.</li>
	<li>Incubate the tubes at 37 &deg;C with orbital agitation at 150 rpm.</li>
	<li>At pre-determined time points (e.g. 0, 1, and 2 hr), mix the solutions in each tube via repeat pipetting (this step is important since bacteria may be trapped inside the PRP gel). Take 10 &mu;l of sample, dilute serially with sterile 0.9% saline, and pipette a 100 &mu;l aliquot of each dilution onto a Tryptic soy agar (TSA, with 5% sheep blood) plate for CFU counting.</li>
	<li>Culture the agar plates overnight at 37 &deg;C, then count and record the plate colonies. Plot data on a logarithimic scale with time (hr) on the x-axis and CFU/ml on the y-axis.</li>
</ol>

<ol><li>Gristina, A. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Biomaterial-centered+infection%3A+microbial+adhesion+versus+tissue+integration%5BTitle%5D)+AND+%22Science%22%5BJournal%5D)">Biomaterial-centered infection: microbial adhesion versus tissue integration.</a> Science. 237, 1588-1595 (1987).</li>
<li>Gristina, A. G., Costerton, J. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Bacterial+adherence+to+biomaterials+and+tissue.+The+significance+of+its+role+in+clinical+sepsis%5BTitle%5D)+AND+%22J.+Bone+Joint+Surg.+Am%22%5BJournal%5D)">Bacterial adherence to biomaterials and tissue. The significance of its role in clinical sepsis.</a> J. Bone Joint Surg. Am. 67, 264-273 (1985).</li>
<li>Everts, P. A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Reviewing+the+structural+features+of+autologous+platelet-leukocyte+gel+and+suggestions+for+use+in+surgery%5BTitle%5D)+AND+%22Eur.+Surg.+Res%22%5BJournal%5D)">Reviewing the structural features of autologous platelet-leukocyte gel and suggestions for use in surgery.</a> Eur. Surg. Res. 39, 199-207 (2007).</li>
<li>Marx, R. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Platelet-rich+plasma+%28PRP%29%3A+what+is+PRP+and+what+is+not+PRP%5BTitle%5D)+AND+%22Implant.+Dent%22%5BJournal%5D)">Platelet-rich plasma (PRP): what is PRP and what is not PRP.</a> Implant. Dent. 10, 225-228 (2001).</li>
<li>Toscano, N., Holtzclaw, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Surgical+considerations+in+the+use+of+platelet-rich+plasma%5BTitle%5D)+AND+%22Compend.+Contin.+Educ.+Dent%22%5BJournal%5D)">Surgical considerations in the use of platelet-rich plasma.</a> Compend. Contin. Educ. Dent. 29, 182-185 (2008).</li>
<li>Cieslik-Bielecka, A., Gazdzik, T. S., Bielecki, T. M., Cieslik, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Why+the+platelet-rich+gel+has+antimicrobial+activity%3F%5BTitle%5D)+AND+%22Oral+Surg.+Oral+Med.+Oral+Pathol.+Oral+Radiol.+Endod%22%5BJournal%5D)">Why the platelet-rich gel has antimicrobial activity?</a> Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod. 103, 303-306 (2007).</li>
<li>Yeaman, M. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+role+of+platelets+in+antimicrobial+host+defense%5BTitle%5D)+AND+%22Clin.+Infect.+Dis%22%5BJournal%5D)">The role of platelets in antimicrobial host defense.</a> Clin. Infect. Dis. 25, 951-970 (1997).</li>
<li>Tang, Y. Q., Yeaman, M. R., Selsted, M. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Antimicrobial+peptides+from+human+platelets%5BTitle%5D)+AND+%22Infect+Immun%22%5BJournal%5D)">Antimicrobial peptides from human platelets.</a> Infect Immun. 70, 6524-6533 (2002).</li>
<li>El-Sharkawy, H., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Platelet-rich+plasma%3A+growth+factors+and+pro-+and+anti-inflammatory+properties%5BTitle%5D)+AND+%22J.+Periodontol%22%5BJournal%5D)">Platelet-rich plasma: growth factors and pro- and anti-inflammatory properties.</a> J. Periodontol. 78, 661-669 (2007).</li>
<li>Krijgsveld, J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Thrombocidins%2C+microbicidal+proteins+from+human+blood+platelets%2C+are+C-terminal+deletion+products+of+CXC+chemokines%5BTitle%5D)+AND+%22J.+Biol.+Chem%22%5BJournal%5D)">Thrombocidins, microbicidal proteins from human blood platelets, are C-terminal deletion products of CXC chemokines.</a> J. Biol. Chem. 275, 20374-20381 (2000).</li>
<li>Trowbridge, C. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Use+of+platelet+gel+and+its+effects+on+infection+in+cardiac+surgery%5BTitle%5D)+AND+%22J.+Extra+Corpor.+Technol%22%5BJournal%5D)">Use of platelet gel and its effects on infection in cardiac surgery.</a> J. Extra Corpor. Technol. 37, 381-386 (2005).</li>
<li>Gristina, A. G., Naylor, P., Myrvik, Q. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Infections+from+biomaterials+and+implants%3A+a+race+for+the+surface%5BTitle%5D)+AND+%22Med.+Prog.+Technol%22%5BJournal%5D)">Infections from biomaterials and implants: a race for the surface.</a> Med. Prog. Technol. 14, 205-224 (1988).</li>
<li>Subbiahdoss, G., Kuijer, R., Grijpma, D. W., vander Mei, H. C., Busscher, H. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Microbial+biofilm+growth+vs.+tissue+integration%3A+%22the+race+for+the+surface%22+experimentally+studied%5BTitle%5D)+AND+%22Acta+Biomater%22%5BJournal%5D)">Microbial biofilm growth vs. tissue integration: "the race for the surface" experimentally studied.</a> Acta Biomater. 5, 1399-1404 (2009).</li>
<li>Klevens, R. M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Invasive+methicillin-resistant+Staphylococcus+aureus+infections+in+the+United+States%5BTitle%5D)+AND+%22JAMA%22%5BJournal%5D)">Invasive methicillin-resistant Staphylococcus aureus infections in the United States.</a> JAMA. 298, 1763-1771 (2007).</li>
<li>Foster, T. E., Puskas, B. L., Mandelbaum, B. R., Gerhardt, M. B., Rodeo, S. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Platelet-rich+plasma%3A+from+basic+science+to+clinical+applications%5BTitle%5D)+AND+%22Am.+J.+Sports+Med%22%5BJournal%5D)">Platelet-rich plasma: from basic science to clinical applications.</a> Am. J. Sports Med. 37, 2259-2272 (2009).</li>
<li>Carlson, N. E., Roach, R. B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Platelet-rich+plasma%3A+clinical+applications+in+dentistry%5BTitle%5D)+AND+%22J.+Am.+Dent.+Assoc%22%5BJournal%5D)">Platelet-rich plasma: clinical applications in dentistry.</a> J. Am. Dent. Assoc. 133, 1383-1386 (2002).</li>
<li>Man, D., Plosker, H., Winland-Brown, J. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+use+of+autologous+platelet-rich+plasma+%28platelet+gel%29+and+autologous+platelet-poor+plasma+%28fibrin+glue%29+in+cosmetic+surgery%5BTitle%5D)+AND+%22Plast.+Reconstr.+Surg%22%5BJournal%5D)">The use of autologous platelet-rich plasma (platelet gel) and autologous platelet-poor plasma (fibrin glue) in cosmetic surgery.</a> Plast. Reconstr. Surg. 107, 229-237 (2001).</li>
<li>Fridkin, S. K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Epidemiological+and+microbiological+characterization+of+infections+caused+by+Staphylococcus+aureus+with+reduced+susceptibility+to+vancomycin%2C+United+States%2C+1997-2001%5BTitle%5D)+AND+%22Clin.+Infect.+Dis%22%5BJournal%5D)">Epidemiological and microbiological characterization of infections caused by Staphylococcus aureus with reduced susceptibility to vancomycin, United States, 1997-2001.</a> Clin. Infect. Dis. 36, 429-439 (1997).</li>
<li>Jackson, C. R., Fedorka-Cray, P. J., Davis, J. A., Barrett, J. B., Frye, J. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Prevalence%2C+species+distribution+and+antimicrobial+resistance+of+enterococci+isolated+from+dogs+and+cats+in+the+United+States%5BTitle%5D)+AND+%22J.+Appl.+Microbiol%22%5BJournal%5D)">Prevalence, species distribution and antimicrobial resistance of enterococci isolated from dogs and cats in the United States.</a> J. Appl. Microbiol. 107, 1269-1278 (2009).</li>
<li>Murray, C. K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Recovery+of+multidrug-resistant+bacteria+from+combat+personnel+evacuated+from+Iraq+and+Afghanistan+at+a+single+military+treatment+facility%5BTitle%5D)+AND+%22Mil.+Med%22%5BJournal%5D)">Recovery of multidrug-resistant bacteria from combat personnel evacuated from Iraq and Afghanistan at a single military treatment facility.</a> Mil. Med. 174, 598-604 (2009).</li>
<li>Durr, M., Peschel, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Chemokines+meet+defensins%3A+the+merging+concepts+of+chemoattractants+and+antimicrobial+peptides+in+host+defense%5BTitle%5D)+AND+%22Infect+Immun%22%5BJournal%5D)">Chemokines meet defensins: the merging concepts of chemoattractants and antimicrobial peptides in host defense.</a> Infect Immun. 70, 6515-6517 (2002).</li>
<li>Hancock, R. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Peptide+antibiotics%5BTitle%5D)+AND+%22Lancet%22%5BJournal%5D)">Peptide antibiotics.</a> Lancet. 349, 418-422 (1997).</li>
<li>Dohan Ehrenfest, D. M., Rasmusson, L., Albrektsson, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Classification+of+platelet+concentrates%3A+from+pure+platelet-rich+plasma+%28P-PRP%29+to+leucocyte-+and+platelet-rich+fibrin+%28L-PRF%29%5BTitle%5D)+AND+%22Trends+Biotechnol%22%5BJournal%5D)">Classification of platelet concentrates: from pure platelet-rich plasma (P-PRP) to leucocyte- and platelet-rich fibrin (L-PRF).</a> Trends Biotechnol. 27, 158-167 (2009).</li>
<li>Kalen, A., Wahlstrom, O., Linder, C. H., Magnusson, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+content+of+bone+morphogenetic+proteins+in+platelets+varies+greatly+between+different+platelet+donors%5BTitle%5D)+AND+%22Biochem.+Biophys.+Res.+Commun%22%5BJournal%5D)">The content of bone morphogenetic proteins in platelets varies greatly between different platelet donors.</a> Biochem. Biophys. Res. Commun. 375, 261-264 (2008).</li>
<li>Weibrich, G., Kleis, W. K., Hafner, G., Hitzler, W. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Growth+factor+levels+in+platelet-rich+plasma+and+correlations+with+donor+age%2C+sex%2C+and+platelet+count%5BTitle%5D)+AND+%22J.+Craniomaxillofac.+Surg%22%5BJournal%5D)">Growth factor levels in platelet-rich plasma and correlations with donor age, sex, and platelet count.</a> J. Craniomaxillofac. Surg. 30, 97-102 (2002).</li>
<li>Mazzucco, L., Balbo, V., Cattana, E., Guaschino, R., Borzini, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Not+every+PRP-gel+is+born+equal.+Evaluation+of+growth+factor+availability+for+tissues+through+four+PRP-gel+preparations%3A+Fibrinet%2C+RegenPRP-Kit%2C+Plateltex+and+one+manual+procedure%5BTitle%5D)+AND+%22Vox+Sang%22%5BJournal%5D)">Not every PRP-gel is born equal. Evaluation of growth factor availability for tissues through four PRP-gel preparations: Fibrinet, RegenPRP-Kit, Plateltex and one manual procedure.</a> Vox Sang. 97, 110-118 (2009).</li>
<li>Lei, H., Gui, L., Xiao, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+effect+of+anticoagulants+on+the+quality+and+biological+efficacy+of+platelet-rich+plasma%5BTitle%5D)+AND+%22Clin.+Biochem%22%5BJournal%5D)">The effect of anticoagulants on the quality and biological efficacy of platelet-rich plasma.</a> Clin. Biochem. 42, 1452-1460 (2009).</li>
<li>Redler, L. H., Thompson, S. A., Hsu, S. H., Ahmad, C. S., Levine, W. N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Platelet-rich+plasma+therapy%3A+a+systematic+literature+review+and+evidence+for+clinical+use%5BTitle%5D)+AND+%22Phys.+Sportsmed%22%5BJournal%5D)">Platelet-rich plasma therapy: a systematic literature review and evidence for clinical use.</a> Phys. Sportsmed. 39, 42-51 (2011).</li>
<li>Whitman, D. H., Berry, R. L., Green, D. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Platelet+gel%3A+an+autologous+alternative+to+fibrin+glue+with+applications+in+oral+and+maxillofacial+surgery%5BTitle%5D)+AND+%22J.+Oral+Maxillofac.+Surg%22%5BJournal%5D)">Platelet gel: an autologous alternative to fibrin glue with applications in oral and maxillofacial surgery.</a> J. Oral Maxillofac. Surg. 55, 1294-1299 (1997).</li>
<li>Anitua, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Plasma+rich+in+growth+factors%3A+preliminary+results+of+use+in+the+preparation+of+future+sites+for+implants%5BTitle%5D)+AND+%22Int.+J.+Oral+Maxillofac.+Implants%22%5BJournal%5D)">Plasma rich in growth factors: preliminary results of use in the preparation of future sites for implants.</a> Int. J. Oral Maxillofac. Implants. 14, 529-535 (1999).</li>
<li>Whitman, D. H., Berry, R. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((A+technique+for+improving+the+handling+of+particulate+cancellous+bone+and+marrow+grafts+using+platelet+gel%5BTitle%5D)+AND+%22J.+Oral.+Maxillofac.+Surg%22%5BJournal%5D)">A technique for improving the handling of particulate cancellous bone and marrow grafts using platelet gel.</a> J. Oral. Maxillofac. Surg. 56, 1217-1218 (1998).</li>
<li>Currie, L. J., Sharpe, J. R., Martin, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+use+of+fibrin+glue+in+skin+grafts+and+tissue-engineered+skin+replacements%3A+a+review%5BTitle%5D)+AND+%22Plast.+Reconstr.+Surg%22%5BJournal%5D)">The use of fibrin glue in skin grafts and tissue-engineered skin replacements: a review.</a> Plast. Reconstr. Surg. 108, 1713-1726 (2001).</li>
<li>Nikulin, A. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Effect+of+calcium%2C+thrombin+and+nucleotides+%28ADP%2C+cAMP%2C+cGMP%29+on+blood+platelet+glycolysis+and+energy+metabolism%5BTitle%5D)+AND+%22Farmakol.+Toksikol%22%5BJournal%5D)">Effect of calcium, thrombin and nucleotides (ADP, cAMP, cGMP) on blood platelet glycolysis and energy metabolism.</a> Farmakol. Toksikol. 43, 585-590 (1980).</li>
<li>Hantgan, R. R., Taylor, R. G., Lewis, J. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Platelets+interact+with+fibrin+only+after+activation%5BTitle%5D)+AND+%22Blood%22%5BJournal%5D)">Platelets interact with fibrin only after activation.</a> Blood. 65, 1299-1311 (1985).</li>
<li>Hantgan, R., Fowler, W., Erickson, H., Hermans, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Fibrin+assembly%3A+a+comparison+of+electron+microscopic+and+light+scattering+results%5BTitle%5D)+AND+%22Thromb.+Haemost%22%5BJournal%5D)">Fibrin assembly: a comparison of electron microscopic and light scattering results.</a> Thromb. Haemost. 44, 119-124 (1980).</li>
<li>Li, B., Jiang, B., Boyce, B. M., Lindsey, B. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Multilayer+polypeptide+nanoscale+coatings+incorporating+IL-12+for+the+prevention+of+biomedical+device-associated+infections%5BTitle%5D)+AND+%22Biomaterials%22%5BJournal%5D)">Multilayer polypeptide nanoscale coatings incorporating IL-12 for the prevention of biomedical device-associated infections.</a> Biomaterials. 30, 2552-2558 (2009).</li>
<li>Li, B., Jiang, B., Dietz, M. J., Smith, E. S., Clovis, N. B., Rao, K. M. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Evaluation+of+local+MCP-1+and+IL-12+nanocoatings+for+infection+prevention+in+open+fractures%5BTitle%5D)+AND+%22J.+Orthop.+Res%22%5BJournal%5D)">Evaluation of local MCP-1 and IL-12 nanocoatings for infection prevention in open fractures.</a> J. Orthop. Res. 28, 48-54 (2010).</li>
<li>Boyce, B. M., Lindsey, B. A., Clovis, N. B., Smith, E. S., Hobbs, G. R., Hubbard, D. F., Emery, S. E., Barnett, J. B., Li, B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Additive+effects+of+exogenous+IL-12+supplementation+and+antibiotic+treatment+in+infection+prophylaxis%5BTitle%5D)+AND+%22J.+Orthop.+Res%22%5BJournal%5D)">Additive effects of exogenous IL-12 supplementation and antibiotic treatment in infection prophylaxis.</a> J. Orthop. Res. 30 (2), 196-202 (2012).</li>
</ol>

The authors declare that they have no competing financial interests.

Platelet-rich plasma has been increasingly used for clinical applications due to its healing-promoting properties 15-17. In the present study, PRP was presented as a new approach for infection prevention. PRP was found to have strong antimicrobial properties against MRSA, MSSA, Group A Streptococcus, and Neisseria gonorrhoeae. The major advantages of PRP, compared to conventional antibiotic treatments, for infection prevention include: (1) Current antibiotic therapies are facing challenges in...

Implant-associated infection is a significant clinical complication. Staphylococcus aureus (S. aureus) is one of the most common microorganisms isolated from implant-associated infections. It is capable of producing a biofilm that covers the surfaces of implants and may lead to antibiotic-resistant infection 1,2. Treatment of implant-associated infection frequently requires long-term hospitalization for repeated debridements and prolonged parenteral antibiotic therapy. In antibiotic resistant cases, removal of the implant may be necessary. The rising resistance of bacteria to antibiotics has also been referred to by the Centers for Disease Control and Prevention (CDC) as "one of the world's most pressing health problems." In time, without the development of new and effective antimicrobial treatments, it is possible that multi-drug resistant pathogens will be untreatable with conventional antibiotics. Prevention of implant-associated infection is therefore important and novel prophylactic agents or approaches are needed for preventing such infections.
Platelet-rich plasma (PRP) is a concentration of autologous blood that contains over 30 growth factors which can help with bone and bone graft healing 3-5. The application of PRP to enhance bone regeneration and soft tissue maturation has been increasingly reported in clinics because of its high concentration of various growth factors released by platelets.
Several characteristics of PRP indicate that PRP may also have antimicrobial properties 6-9. PRP contains a large number of platelets, a high concentration of leukocytes (which may possess host-defense actions against bacteria and fungi), and multiple antimicrobial peptides 7,8,10. In a recent study of a large cohort of cardiac surgical patients, it was revealed that the intraoperative use of PRP-gel during wound closure significantly decreased the incidence of superficial and deep sternum infection 11. For these reasons and observations, we hypothesized that PRP, besides its well-studied healing-promoting properties, has antimicrobial properties. The potential advantages of using PRP to prevent infection may include: (i) PRP is less likely to induce resistance compared to conventional antibiotic treatments. (ii) PRP also has properties that promote healing which may have a synergistic effect on infection prevention; PRP's healing-promoting properties could provide a seal to prevent bacterial attachment thereby reducing the odds for infection as pathogens and human cells are racing for implant surfaces 12,13. (iii) PRP is inherently biocompatible, and safe and free from the risk of transmissible diseases.
Our long-term goal is to use PRP as a new approach to prevent implant-associated infections. The aim of this study was to prepare PRP using a twice centrifugation approach, to examine PRP's in vitro antimicrobial properties, and to describe the protocols for evaluating such antimicrobial properties.

<table><tbody><tr><td>Bovine thrombin</td><td>King Pharmaceuticals, Inc</td><td>60793-215-05</td><td>Thrombin (bovine origin)</td></tr><tr><td>Calcium chloride</td><td>King Pharmaceuticals, Inc</td><td>60793-215-05</td><td>10% calcium chloride</td></tr><tr><td>Ethanol</td><td>Sigma-Aldrich</td><td>E7023</td><td></td></tr><tr><td>Isoflurane</td><td>Baxter</td><td>1001936060</td><td></td></tr><tr><td>Mueller Hinton broth</td><td>Becton, Dickinson and Company</td><td>275710</td><td></td></tr><tr><td>Phosphate-buffered saline</td><td>Sigma-Aldrich</td><td>D8662</td><td></td></tr><tr><td>Tri-sodium citrate</td><td>Sigma-Aldrich</td><td>W302600</td><td></td></tr><tr><td>Tryptic soy agar</td><td>Fisher Scientific</td><td>R01202</td><td></td></tr><tr><td>Centrifuge</td><td>Kendro Laboratory Products</td><td>750043077</td><td></td></tr><tr><td>Syringe filter</td><td>Millipore</td><td>SLGP033RS</td><td></td></tr></tbody></table>

prp as a new approach to prevent infection: preparation and in vitro antimicrobial properties of prp

PRP as a New Approach to Prevent Infection: Preparation and In vitro Antimicrobial Properties of PRP

Implant-associated infection is becoming more and more challenging to the healthcare industry worldwide due to increasing antibiotic resistance, transmission of antibiotic resistant bacteria between animals and humans, and the high cost of treating infections.
In this study, we disclose a new strategy that may be effective in preventing implant-associated infection based on the potential antimicrobial properties of platelet-rich plasma (PRP). Due to its well-studied properties for promoting healing, PRP (a biological product) has been increasingly used for clinical applications including orthopaedic surgeries, periodontal and oral surgeries, maxillofacial surgeries, plastic surgeries, sports medicine, etc.
PRP could be an advanced alternative to conventional antibiotic treatments in preventing implant-associated infections. The use of PRP may be advantageous compared to conventional antibiotic treatments since PRP is less likely to induce antibiotic resistance and PRP's antimicrobial and healing-promoting properties may have a synergistic effect on infection prevention. It is well known that pathogens and human cells are racing for implant surfaces, and PRP's properties of promoting healing could improve human cell attachment thereby reducing the odds for infection. In addition, PRP is inherently biocompatible, and safe and free from the risk of transmissible diseases.
For our study, we have selected several clinical bacterial strains that are commonly found in orthopaedic infections and examined whether PRP has in vitro antimicrobial properties against these bacteria. We have prepared PRP using a twice centrifugation approach which allows the same platelet concentration to be obtained for all samples. We have achieved consistent antimicrobial findings and found that PRP has strong in vitro antimicrobial properties against bacteria like methicillin-sensitive and methicillin-resistant Staphylococcus aureus, Group A Streptococcus, and Neisseria gonorrhoeae. Therefore, the use of PRP may have the potential to prevent infection and to reduce the need for costly post-operative treatment of implant-associated infections.

PRP is reproducibly prepared using a twice centrifugation approach (Figure 1). PRP is found to present strong (up to 100-fold reduction in CFUs) in vitro antimicrobial properties against methicillin resistant S. aureus (MRSA) (Figure 3), which is commonly found in hospitals worldwide 14. Similarly, PRP has strong antimicrobial properties against methicillin sensitive S. aureus (MSSA), Group A Streptococcus, and Neisseria gonorrhoeae...

Implant-associated infection is a significant clinical complication. This study describes an approach using platelet-rich plasma (PRP) to prevent implant-associated infections, presents the protocol for preparing PRP with constant platelet concentration, and reports the newly identified antimicrobial properties of PRP and related protocols for examining such antimicrobial properties in vitro.

Implant-associated infection is becoming more and more challenging to the healthcare industry worldwide due to increasing antibiotic resistance, ...

The overall goal of this procedure is to examine platelet rich plasma or PRPs in vitro antimicrobial properties. First, isolate platelet rich plasma from a donor rabbit. Next, prepare a bacterial inoculum, then activate the PRP using thrombin and mix with the bacterial inoculum.Incubate the mixture, sample, and measure the resulting colony forming units. The antimicrobial properties of PRP are demonstrated by the reduction of CFU in PRP treated samples compared to the control samples. Without PRP treatment, Platelet reach plasma is less likely to induce BOL resistance compared to conventional BOL treatments.It also has properties that promote wound healing, which may have a synergistic effect on infection prevention. In the current protocol, a twice ification approach was performed and the platelet concentration of PRP was standardized to two times 10 to the six platelets per approximately 10 times above the baseline in blood, leukocyte reached PRP was used. Since leukocytes are also involved in direct bacterial kidney and antigen specific immune response, which may contribute to the antimicrobial properties of PRP First anesthetize a rabbit by inhalation of isof fluorine.Draw two

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Learn to prepare platelet-rich plasma and evaluate its antimicrobial properties against bacteria in vitro. This method demonstrates significant CFU reduction and supports infection prevention strategies.

PRP as a New Approach to Prevent Infection: Preparation and In vitro Antimicrobial Properties of PRP

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