Vancomycin-Loaded Collagen/Hydroxyapatite Layers Electrospun on 3D Printed Titanium Implants Prevent Bone Destruction Associated with <i>S. epidermidis</i> Infection and Enhance Osseointegration
The aim of the study was to develop an orthopedic implant coating in the form of vancomycin-loaded collagen/hydroxyapatite layers (COLHA+V) that combine the ability to prevent bone infection with the ability to promote enhanced osseointegration. The ability to prevent bone infection was investigated...
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MDPI AG
2021-05-01
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Series: | Biomedicines |
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Online Access: | https://www.mdpi.com/2227-9059/9/5/531 |
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doaj-577cd713698545d6a037727e96c05852 |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tomáš Suchý Lucie Vištejnová Monika Šupová Pavel Klein Martin Bartoš Yaroslav Kolinko Tereza Blassová Zbyněk Tonar Marek Pokorný Zbyněk Sucharda Margit Žaloudková František Denk Rastislav Ballay Štefan Juhás Jana Juhásová Eva Klapková Lukáš Horný Radek Sedláček Tomáš Grus Zdeněk Čejka Zdeněk Čejka Kateřina Chudějová Jaroslav Hrabák |
spellingShingle |
Tomáš Suchý Lucie Vištejnová Monika Šupová Pavel Klein Martin Bartoš Yaroslav Kolinko Tereza Blassová Zbyněk Tonar Marek Pokorný Zbyněk Sucharda Margit Žaloudková František Denk Rastislav Ballay Štefan Juhás Jana Juhásová Eva Klapková Lukáš Horný Radek Sedláček Tomáš Grus Zdeněk Čejka Zdeněk Čejka Kateřina Chudějová Jaroslav Hrabák Vancomycin-Loaded Collagen/Hydroxyapatite Layers Electrospun on 3D Printed Titanium Implants Prevent Bone Destruction Associated with <i>S. epidermidis</i> Infection and Enhance Osseointegration Biomedicines orthopedic implant collagen hydroxyapatite vancomycin implant-related bone infection <i>Staphylococcus epidermidis</i> |
author_facet |
Tomáš Suchý Lucie Vištejnová Monika Šupová Pavel Klein Martin Bartoš Yaroslav Kolinko Tereza Blassová Zbyněk Tonar Marek Pokorný Zbyněk Sucharda Margit Žaloudková František Denk Rastislav Ballay Štefan Juhás Jana Juhásová Eva Klapková Lukáš Horný Radek Sedláček Tomáš Grus Zdeněk Čejka Zdeněk Čejka Kateřina Chudějová Jaroslav Hrabák |
author_sort |
Tomáš Suchý |
title |
Vancomycin-Loaded Collagen/Hydroxyapatite Layers Electrospun on 3D Printed Titanium Implants Prevent Bone Destruction Associated with <i>S. epidermidis</i> Infection and Enhance Osseointegration |
title_short |
Vancomycin-Loaded Collagen/Hydroxyapatite Layers Electrospun on 3D Printed Titanium Implants Prevent Bone Destruction Associated with <i>S. epidermidis</i> Infection and Enhance Osseointegration |
title_full |
Vancomycin-Loaded Collagen/Hydroxyapatite Layers Electrospun on 3D Printed Titanium Implants Prevent Bone Destruction Associated with <i>S. epidermidis</i> Infection and Enhance Osseointegration |
title_fullStr |
Vancomycin-Loaded Collagen/Hydroxyapatite Layers Electrospun on 3D Printed Titanium Implants Prevent Bone Destruction Associated with <i>S. epidermidis</i> Infection and Enhance Osseointegration |
title_full_unstemmed |
Vancomycin-Loaded Collagen/Hydroxyapatite Layers Electrospun on 3D Printed Titanium Implants Prevent Bone Destruction Associated with <i>S. epidermidis</i> Infection and Enhance Osseointegration |
title_sort |
vancomycin-loaded collagen/hydroxyapatite layers electrospun on 3d printed titanium implants prevent bone destruction associated with <i>s. epidermidis</i> infection and enhance osseointegration |
publisher |
MDPI AG |
series |
Biomedicines |
issn |
2227-9059 |
publishDate |
2021-05-01 |
description |
The aim of the study was to develop an orthopedic implant coating in the form of vancomycin-loaded collagen/hydroxyapatite layers (COLHA+V) that combine the ability to prevent bone infection with the ability to promote enhanced osseointegration. The ability to prevent bone infection was investigated employing a rat model that simulated the clinically relevant implant-related introduction of bacterial contamination to the bone during a surgical procedure using a clinical isolate of <i>Staphylococcus epidermidis</i>. The ability to enhance osseointegration was investigated employing a model of a minipig with terminated growth. Six weeks following implantation, the infected rat femurs treated with the implants without vancomycin (COLHA+<i>S. epidermidis</i>) exhibited the obvious destruction of cortical bone as evinced via a cortical bone porosity of up to 20% greater than that of the infected rat femurs treated with the implants containing vancomycin (COLHA+V+<i>S. epidermidis</i>) (3%) and the non-infected rat femurs (COLHA+V) (2%). The alteration of the bone structure of the infected COLHA+<i>S. epidermidis</i> group was further demonstrated by a 3% decrease in the average Ca/P molar ratio of the bone mineral. Finally, the determination of the concentration of vancomycin released into the blood stream indicated a negligible systemic load. Six months following implantation in the pigs, the quantified ratio of new bone indicated an improvement in osseointegration, with a two-fold bone ingrowth on the COLHA (47%) and COLHA+V (52%) compared to the control implants without a COLHA layer (27%). Therefore, it can be concluded that COLHA+V layers are able to significantly prevent the destruction of bone structure related to bacterial infection with a minimal systemic load and, simultaneously, enhance the rate of osseointegration. |
topic |
orthopedic implant collagen hydroxyapatite vancomycin implant-related bone infection <i>Staphylococcus epidermidis</i> |
url |
https://www.mdpi.com/2227-9059/9/5/531 |
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doaj-577cd713698545d6a037727e96c058522021-05-31T23:37:04ZengMDPI AGBiomedicines2227-90592021-05-01953153110.3390/biomedicines9050531Vancomycin-Loaded Collagen/Hydroxyapatite Layers Electrospun on 3D Printed Titanium Implants Prevent Bone Destruction Associated with <i>S. epidermidis</i> Infection and Enhance OsseointegrationTomáš Suchý0Lucie Vištejnová1Monika Šupová2Pavel Klein3Martin Bartoš4Yaroslav Kolinko5Tereza Blassová6Zbyněk Tonar7Marek Pokorný8Zbyněk Sucharda9Margit Žaloudková10František Denk11Rastislav Ballay12Štefan Juhás13Jana Juhásová14Eva Klapková15Lukáš Horný16Radek Sedláček17Tomáš Grus18Zdeněk Čejka19Zdeněk Čejka20Kateřina Chudějová21Jaroslav Hrabák22Department of Composites and Carbon Materials, Institute of Rock Structure and Mechanics, Czech Academy of Sciences, 18209 Prague 8, Czech RepublicBiomedical Center, Faculty of Medicine in Pilsen, Charles University, 30100 Pilsen, Czech RepublicDepartment of Composites and Carbon Materials, Institute of Rock Structure and Mechanics, Czech Academy of Sciences, 18209 Prague 8, Czech RepublicBiomedical Center, Faculty of Medicine in Pilsen, Charles University, 30100 Pilsen, Czech RepublicBiomedical Center, Faculty of Medicine in Pilsen, Charles University, 30100 Pilsen, Czech RepublicBiomedical Center, Faculty of Medicine in Pilsen, Charles University, 30100 Pilsen, Czech RepublicBiomedical Center, Faculty of Medicine in Pilsen, Charles University, 30100 Pilsen, Czech RepublicBiomedical Center, Faculty of Medicine in Pilsen, Charles University, 30100 Pilsen, Czech RepublicR&D Department, Contipro Inc., 56102 Dolni Dobrouc, Czech RepublicDepartment of Composites and Carbon Materials, Institute of Rock Structure and Mechanics, Czech Academy of Sciences, 18209 Prague 8, Czech RepublicDepartment of Composites and Carbon Materials, Institute of Rock Structure and Mechanics, Czech Academy of Sciences, 18209 Prague 8, Czech RepublicDepartment of Composites and Carbon Materials, Institute of Rock Structure and Mechanics, Czech Academy of Sciences, 18209 Prague 8, Czech Republic1st Department of Orthopedics, First Faculty of Medicine, Charles University in Prague and Motol University Hospital, 150 06 Prague 5, Czech RepublicPIGMOD Centre, Laboratory of Cell Regeneration and Plasticity, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, 27721 Libechov, Czech RepublicPIGMOD Centre, Laboratory of Cell Regeneration and Plasticity, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, 27721 Libechov, Czech RepublicDepartment of Medical Chemistry and Clinical Biochemistry, Charles University, 2nd Medical School and University Hospital Motol, 15006 Prague 5, Czech RepublicFaculty of Mechanical Engineering, Czech Technical University in Prague, 16000 Prague 6, Czech RepublicFaculty of Mechanical Engineering, Czech Technical University in Prague, 16000 Prague 6, Czech Republic2nd Department of Cardiovascular Surgery, First Faculty of Medicine, Charles University and General University Hospital in Prague, 12000 Prague 2, Czech RepublicProSpon Ltd., 27201 Kladno, Czech RepublicProSpon Ltd., 27201 Kladno, Czech RepublicBiomedical Center, Faculty of Medicine in Pilsen, Charles University, 30100 Pilsen, Czech RepublicBiomedical Center, Faculty of Medicine in Pilsen, Charles University, 30100 Pilsen, Czech RepublicThe aim of the study was to develop an orthopedic implant coating in the form of vancomycin-loaded collagen/hydroxyapatite layers (COLHA+V) that combine the ability to prevent bone infection with the ability to promote enhanced osseointegration. The ability to prevent bone infection was investigated employing a rat model that simulated the clinically relevant implant-related introduction of bacterial contamination to the bone during a surgical procedure using a clinical isolate of <i>Staphylococcus epidermidis</i>. The ability to enhance osseointegration was investigated employing a model of a minipig with terminated growth. Six weeks following implantation, the infected rat femurs treated with the implants without vancomycin (COLHA+<i>S. epidermidis</i>) exhibited the obvious destruction of cortical bone as evinced via a cortical bone porosity of up to 20% greater than that of the infected rat femurs treated with the implants containing vancomycin (COLHA+V+<i>S. epidermidis</i>) (3%) and the non-infected rat femurs (COLHA+V) (2%). The alteration of the bone structure of the infected COLHA+<i>S. epidermidis</i> group was further demonstrated by a 3% decrease in the average Ca/P molar ratio of the bone mineral. Finally, the determination of the concentration of vancomycin released into the blood stream indicated a negligible systemic load. Six months following implantation in the pigs, the quantified ratio of new bone indicated an improvement in osseointegration, with a two-fold bone ingrowth on the COLHA (47%) and COLHA+V (52%) compared to the control implants without a COLHA layer (27%). Therefore, it can be concluded that COLHA+V layers are able to significantly prevent the destruction of bone structure related to bacterial infection with a minimal systemic load and, simultaneously, enhance the rate of osseointegration.https://www.mdpi.com/2227-9059/9/5/531orthopedic implantcollagenhydroxyapatitevancomycinimplant-related bone infection<i>Staphylococcus epidermidis</i> |