Biodegradable composites with antibiotics and growth factors for dual release kinetics

Abstract Bone infections are still a major problem in surgery. To avoid severe side effects of systemically administered antibiotics, local antibiotic therapy is increasingly being considered. Using a pressure-based method developed in our group, microporous β-TCP ceramics, which had previously been...

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Main Authors: Michael Seidenstuecker, Julian Hess, Anna Baghnavi, Hagen Schmal, Diana Voigt, Hermann O. Mayr
Format: Article
Language:English
Published: Springer 2024-07-01
Series:Journal of Materials Science: Materials in Medicine
Online Access:https://doi.org/10.1007/s10856-024-06809-8
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author Michael Seidenstuecker
Julian Hess
Anna Baghnavi
Hagen Schmal
Diana Voigt
Hermann O. Mayr
author_facet Michael Seidenstuecker
Julian Hess
Anna Baghnavi
Hagen Schmal
Diana Voigt
Hermann O. Mayr
author_sort Michael Seidenstuecker
collection DOAJ
description Abstract Bone infections are still a major problem in surgery. To avoid severe side effects of systemically administered antibiotics, local antibiotic therapy is increasingly being considered. Using a pressure-based method developed in our group, microporous β-TCP ceramics, which had previously been characterized, were loaded with 2% w/v alginate containing 50 mg/mL clindamycin and 10 µg/mL rhBMP-2. Release experiments were then carried out over 28 days with changes of liquid at defined times (1, 2, 3, 6, 9, 14, 21 and 28d). The released concentrations of clindamycin were determined by HPLC and those of rhBMP-2 by ELISA. Continuous release (anomalous transport) of clindamycin and uniform release (Fick’s diffusion) of BMP-2 were determined. The composites were biocompatible (live/dead, WST-I and LDH) and the released concentrations were all antimicrobially active against Staph. aureus. The results were very promising and clindamycin was detected in concentrations above the MIC as well as a constant rhBMP-2 release over the entire study period. Biocompatibility was also not impaired by either the antibiotic or the BMP-2. This promising approach can therefore be seen as an alternative to the common treatment with PMMA chains containing gentamycin, as the new composite is completely biodegradable and no second operation is necessary for removal or replacement. Graphical Abstract
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spelling doaj-art-7dd8288bbc754fa58499505463b8c1212025-08-20T01:59:47ZengSpringerJournal of Materials Science: Materials in Medicine1573-48382024-07-0135111510.1007/s10856-024-06809-8Biodegradable composites with antibiotics and growth factors for dual release kineticsMichael Seidenstuecker0Julian Hess1Anna Baghnavi2Hagen Schmal3Diana Voigt4Hermann O. Mayr5G.E.R.N. Center of Tissue Replacement, Regeneration & Neogenesis, Department of Orthopedics and Trauma Surgery, Medical Center—Albert-Ludwigs-University of Freiburg, Faculty of Medicine, Albert-Ludwigs-University of FreiburgG.E.R.N. Center of Tissue Replacement, Regeneration & Neogenesis, Department of Orthopedics and Trauma Surgery, Medical Center—Albert-Ludwigs-University of Freiburg, Faculty of Medicine, Albert-Ludwigs-University of FreiburgG.E.R.N. Center of Tissue Replacement, Regeneration & Neogenesis, Department of Orthopedics and Trauma Surgery, Medical Center—Albert-Ludwigs-University of Freiburg, Faculty of Medicine, Albert-Ludwigs-University of FreiburgDepartment of Orthopedics and Trauma Surgery, Medical Center—Albert-Ludwigs-University of Freiburg, Faculty of Medicine, Albert-Ludwigs-University of FreiburgFILK Freiberg Institute gGmbHDepartment of Orthopedics and Trauma Surgery, Medical Center—Albert-Ludwigs-University of Freiburg, Faculty of Medicine, Albert-Ludwigs-University of FreiburgAbstract Bone infections are still a major problem in surgery. To avoid severe side effects of systemically administered antibiotics, local antibiotic therapy is increasingly being considered. Using a pressure-based method developed in our group, microporous β-TCP ceramics, which had previously been characterized, were loaded with 2% w/v alginate containing 50 mg/mL clindamycin and 10 µg/mL rhBMP-2. Release experiments were then carried out over 28 days with changes of liquid at defined times (1, 2, 3, 6, 9, 14, 21 and 28d). The released concentrations of clindamycin were determined by HPLC and those of rhBMP-2 by ELISA. Continuous release (anomalous transport) of clindamycin and uniform release (Fick’s diffusion) of BMP-2 were determined. The composites were biocompatible (live/dead, WST-I and LDH) and the released concentrations were all antimicrobially active against Staph. aureus. The results were very promising and clindamycin was detected in concentrations above the MIC as well as a constant rhBMP-2 release over the entire study period. Biocompatibility was also not impaired by either the antibiotic or the BMP-2. This promising approach can therefore be seen as an alternative to the common treatment with PMMA chains containing gentamycin, as the new composite is completely biodegradable and no second operation is necessary for removal or replacement. Graphical Abstracthttps://doi.org/10.1007/s10856-024-06809-8
spellingShingle Michael Seidenstuecker
Julian Hess
Anna Baghnavi
Hagen Schmal
Diana Voigt
Hermann O. Mayr
Biodegradable composites with antibiotics and growth factors for dual release kinetics
Journal of Materials Science: Materials in Medicine
title Biodegradable composites with antibiotics and growth factors for dual release kinetics
title_full Biodegradable composites with antibiotics and growth factors for dual release kinetics
title_fullStr Biodegradable composites with antibiotics and growth factors for dual release kinetics
title_full_unstemmed Biodegradable composites with antibiotics and growth factors for dual release kinetics
title_short Biodegradable composites with antibiotics and growth factors for dual release kinetics
title_sort biodegradable composites with antibiotics and growth factors for dual release kinetics
url https://doi.org/10.1007/s10856-024-06809-8
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