Evaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defect

Abstract We previously reported the development of an osteogenic bone filler scaffold consisting of degradable polyurethane, hydroxyapatite, and decellularized bovine bone particles. The current study was aimed at evaluating the use of this scaffold as a means of local antibiotic delivery to prevent...

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Main Authors: Karen E. Beenken, Mara J. Campbell, Aura M. Ramirez, Karrar Alghazali, Christopher M. Walker, Bailey Jackson, Christopher Griffin, William King, Shawn E. Bourdo, Rebecca Rifkin, Silke Hecht, Daniel G. Meeker, David E. Anderson, Alexandru S. Biris, Mark S. Smeltzer
Format: Article
Language:English
Published: Nature Publishing Group 2021-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-89830-z
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spelling doaj-499612545c514ba09349c6d9e0ce29072021-05-16T11:25:19ZengNature Publishing GroupScientific Reports2045-23222021-05-0111111010.1038/s41598-021-89830-zEvaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defectKaren E. Beenken0Mara J. Campbell1Aura M. Ramirez2Karrar Alghazali3Christopher M. Walker4Bailey Jackson5Christopher Griffin6William King7Shawn E. Bourdo8Rebecca Rifkin9Silke Hecht10Daniel G. Meeker11David E. Anderson12Alexandru S. Biris13Mark S. Smeltzer14Department of Microbiology and Immunology, University of Arkansas for Medical SciencesDepartment of Microbiology and Immunology, University of Arkansas for Medical SciencesDepartment of Microbiology and Immunology, University of Arkansas for Medical SciencesCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little RockDepartment of Microbiology and Immunology, University of Arkansas for Medical SciencesCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little RockCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little RockCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little RockCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little RockDepartment of Large Animal Clinical Sciences, University of Tennessee College of Veterinary MedicineDepartment of Small Animal Clinical Sciences, University of Tennessee College of Veterinary MedicineDepartment of Microbiology and Immunology, University of Arkansas for Medical SciencesDepartment of Large Animal Clinical Sciences, University of Tennessee College of Veterinary MedicineCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little RockDepartment of Microbiology and Immunology, University of Arkansas for Medical SciencesAbstract We previously reported the development of an osteogenic bone filler scaffold consisting of degradable polyurethane, hydroxyapatite, and decellularized bovine bone particles. The current study was aimed at evaluating the use of this scaffold as a means of local antibiotic delivery to prevent infection in a bone defect contaminated with Staphylococcus aureus. We evaluated two scaffold formulations with the same component ratios but differing overall porosity and surface area. Studies with vancomycin, daptomycin, and gentamicin confirmed that antibiotic uptake was concentration dependent and that increased porosity correlated with increased uptake and prolonged antibiotic release. We also demonstrate that vancomycin can be passively loaded into either formulation in sufficient concentration to prevent infection in a rabbit model of a contaminated segmental bone defect. Moreover, even in those few cases in which complete eradication was not achieved, the number of viable bacteria in the bone was significantly reduced by treatment and there was no radiographic evidence of osteomyelitis. Radiographs and microcomputed tomography (µCT) analysis from the in vivo studies also suggested that the addition of vancomycin did not have any significant effect on the scaffold itself. These results demonstrate the potential utility of our bone regeneration scaffold for local antibiotic delivery to prevent infection in contaminated bone defects.https://doi.org/10.1038/s41598-021-89830-z
collection DOAJ
language English
format Article
sources DOAJ
author Karen E. Beenken
Mara J. Campbell
Aura M. Ramirez
Karrar Alghazali
Christopher M. Walker
Bailey Jackson
Christopher Griffin
William King
Shawn E. Bourdo
Rebecca Rifkin
Silke Hecht
Daniel G. Meeker
David E. Anderson
Alexandru S. Biris
Mark S. Smeltzer
spellingShingle Karen E. Beenken
Mara J. Campbell
Aura M. Ramirez
Karrar Alghazali
Christopher M. Walker
Bailey Jackson
Christopher Griffin
William King
Shawn E. Bourdo
Rebecca Rifkin
Silke Hecht
Daniel G. Meeker
David E. Anderson
Alexandru S. Biris
Mark S. Smeltzer
Evaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defect
Scientific Reports
author_facet Karen E. Beenken
Mara J. Campbell
Aura M. Ramirez
Karrar Alghazali
Christopher M. Walker
Bailey Jackson
Christopher Griffin
William King
Shawn E. Bourdo
Rebecca Rifkin
Silke Hecht
Daniel G. Meeker
David E. Anderson
Alexandru S. Biris
Mark S. Smeltzer
author_sort Karen E. Beenken
title Evaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defect
title_short Evaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defect
title_full Evaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defect
title_fullStr Evaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defect
title_full_unstemmed Evaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defect
title_sort evaluation of a bone filler scaffold for local antibiotic delivery to prevent staphylococcus aureus infection in a contaminated bone defect
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-05-01
description Abstract We previously reported the development of an osteogenic bone filler scaffold consisting of degradable polyurethane, hydroxyapatite, and decellularized bovine bone particles. The current study was aimed at evaluating the use of this scaffold as a means of local antibiotic delivery to prevent infection in a bone defect contaminated with Staphylococcus aureus. We evaluated two scaffold formulations with the same component ratios but differing overall porosity and surface area. Studies with vancomycin, daptomycin, and gentamicin confirmed that antibiotic uptake was concentration dependent and that increased porosity correlated with increased uptake and prolonged antibiotic release. We also demonstrate that vancomycin can be passively loaded into either formulation in sufficient concentration to prevent infection in a rabbit model of a contaminated segmental bone defect. Moreover, even in those few cases in which complete eradication was not achieved, the number of viable bacteria in the bone was significantly reduced by treatment and there was no radiographic evidence of osteomyelitis. Radiographs and microcomputed tomography (µCT) analysis from the in vivo studies also suggested that the addition of vancomycin did not have any significant effect on the scaffold itself. These results demonstrate the potential utility of our bone regeneration scaffold for local antibiotic delivery to prevent infection in contaminated bone defects.
url https://doi.org/10.1038/s41598-021-89830-z
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