Cargando…
Simultaneous Delivery of Multiple Antibacterial Agents from Additively Manufactured Porous Biomaterials to Fully Eradicate Planktonic and Adherent Staphylococcus aureus
[Image: see text] Implant-associated infections are notoriously difficult to treat and may even result in amputation and death. The first few days after surgery are the most critical time to prevent those infections, preferably through full eradication of the micro-organisms entering the body periop...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2017
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5553095/ https://www.ncbi.nlm.nih.gov/pubmed/28696671 http://dx.doi.org/10.1021/acsami.7b04950 |
_version_ | 1783256579594780672 |
---|---|
author | Bakhshandeh, S. Gorgin Karaji, Z. Lietaert, K. Fluit, A. C. Boel, C. H. E. Vogely, H. C. Vermonden, T. Hennink, W. E. Weinans, H. Zadpoor, A. A. Amin Yavari, S. |
author_facet | Bakhshandeh, S. Gorgin Karaji, Z. Lietaert, K. Fluit, A. C. Boel, C. H. E. Vogely, H. C. Vermonden, T. Hennink, W. E. Weinans, H. Zadpoor, A. A. Amin Yavari, S. |
author_sort | Bakhshandeh, S. |
collection | PubMed |
description | [Image: see text] Implant-associated infections are notoriously difficult to treat and may even result in amputation and death. The first few days after surgery are the most critical time to prevent those infections, preferably through full eradication of the micro-organisms entering the body perioperatively. That is particularly important for patients with a compromised immune system such as orthopedic oncology patients, as they are at higher risk for infection and complications. Full eradication of bacteria is, especially in a biofilm, extremely challenging due to the toxicity barrier that prevents delivery of high doses of antibacterial agents. This study aimed to use the potential synergistic effects of multiple antibacterial agents to prevent the use of toxic levels of these agents and achieve full eradication of planktonic and adherent bacteria. Silver ions and vancomycin were therefore simultaneously delivered from additively manufactured highly porous titanium implants with an extremely high surface area incorporating a bactericidal coating made from chitosan and gelatin applied by electrophoretic deposition (EPD). The presence of the chitosan/gelatin (Ch+Gel) coating, Ag, and vancomycin (Vanco) was confirmed by X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR). The release of vancomycin and silver ions continued for at least 21 days as measured by inductively coupled plasma (ICP) and UV-spectroscopy. Antibacterial behavior against Staphylococcus aureus, both planktonic and in biofilm, was evaluated for up to 21 days. The Ch+Gel coating showed some bactericidal behavior on its own, while the loaded hydrogels (Ch+Gel+Ag and Ch+Gel+Vanco) achieved full eradication of both planktonic and adherent bacteria without causing significant levels of toxicity. Combining silver and vancomycin improved the release profiles of both agents and revealed a synergistic behavior that further increased the bactericidal effects. |
format | Online Article Text |
id | pubmed-5553095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-55530952017-08-14 Simultaneous Delivery of Multiple Antibacterial Agents from Additively Manufactured Porous Biomaterials to Fully Eradicate Planktonic and Adherent Staphylococcus aureus Bakhshandeh, S. Gorgin Karaji, Z. Lietaert, K. Fluit, A. C. Boel, C. H. E. Vogely, H. C. Vermonden, T. Hennink, W. E. Weinans, H. Zadpoor, A. A. Amin Yavari, S. ACS Appl Mater Interfaces [Image: see text] Implant-associated infections are notoriously difficult to treat and may even result in amputation and death. The first few days after surgery are the most critical time to prevent those infections, preferably through full eradication of the micro-organisms entering the body perioperatively. That is particularly important for patients with a compromised immune system such as orthopedic oncology patients, as they are at higher risk for infection and complications. Full eradication of bacteria is, especially in a biofilm, extremely challenging due to the toxicity barrier that prevents delivery of high doses of antibacterial agents. This study aimed to use the potential synergistic effects of multiple antibacterial agents to prevent the use of toxic levels of these agents and achieve full eradication of planktonic and adherent bacteria. Silver ions and vancomycin were therefore simultaneously delivered from additively manufactured highly porous titanium implants with an extremely high surface area incorporating a bactericidal coating made from chitosan and gelatin applied by electrophoretic deposition (EPD). The presence of the chitosan/gelatin (Ch+Gel) coating, Ag, and vancomycin (Vanco) was confirmed by X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR). The release of vancomycin and silver ions continued for at least 21 days as measured by inductively coupled plasma (ICP) and UV-spectroscopy. Antibacterial behavior against Staphylococcus aureus, both planktonic and in biofilm, was evaluated for up to 21 days. The Ch+Gel coating showed some bactericidal behavior on its own, while the loaded hydrogels (Ch+Gel+Ag and Ch+Gel+Vanco) achieved full eradication of both planktonic and adherent bacteria without causing significant levels of toxicity. Combining silver and vancomycin improved the release profiles of both agents and revealed a synergistic behavior that further increased the bactericidal effects. American Chemical Society 2017-07-11 2017-08-09 /pmc/articles/PMC5553095/ /pubmed/28696671 http://dx.doi.org/10.1021/acsami.7b04950 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Bakhshandeh, S. Gorgin Karaji, Z. Lietaert, K. Fluit, A. C. Boel, C. H. E. Vogely, H. C. Vermonden, T. Hennink, W. E. Weinans, H. Zadpoor, A. A. Amin Yavari, S. Simultaneous Delivery of Multiple Antibacterial Agents from Additively Manufactured Porous Biomaterials to Fully Eradicate Planktonic and Adherent Staphylococcus aureus |
title | Simultaneous
Delivery of Multiple Antibacterial Agents from Additively Manufactured
Porous Biomaterials to Fully Eradicate Planktonic and Adherent Staphylococcus
aureus |
title_full | Simultaneous
Delivery of Multiple Antibacterial Agents from Additively Manufactured
Porous Biomaterials to Fully Eradicate Planktonic and Adherent Staphylococcus
aureus |
title_fullStr | Simultaneous
Delivery of Multiple Antibacterial Agents from Additively Manufactured
Porous Biomaterials to Fully Eradicate Planktonic and Adherent Staphylococcus
aureus |
title_full_unstemmed | Simultaneous
Delivery of Multiple Antibacterial Agents from Additively Manufactured
Porous Biomaterials to Fully Eradicate Planktonic and Adherent Staphylococcus
aureus |
title_short | Simultaneous
Delivery of Multiple Antibacterial Agents from Additively Manufactured
Porous Biomaterials to Fully Eradicate Planktonic and Adherent Staphylococcus
aureus |
title_sort | simultaneous
delivery of multiple antibacterial agents from additively manufactured
porous biomaterials to fully eradicate planktonic and adherent staphylococcus
aureus |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5553095/ https://www.ncbi.nlm.nih.gov/pubmed/28696671 http://dx.doi.org/10.1021/acsami.7b04950 |
work_keys_str_mv | AT bakhshandehs simultaneousdeliveryofmultipleantibacterialagentsfromadditivelymanufacturedporousbiomaterialstofullyeradicateplanktonicandadherentstaphylococcusaureus AT gorginkarajiz simultaneousdeliveryofmultipleantibacterialagentsfromadditivelymanufacturedporousbiomaterialstofullyeradicateplanktonicandadherentstaphylococcusaureus AT lietaertk simultaneousdeliveryofmultipleantibacterialagentsfromadditivelymanufacturedporousbiomaterialstofullyeradicateplanktonicandadherentstaphylococcusaureus AT fluitac simultaneousdeliveryofmultipleantibacterialagentsfromadditivelymanufacturedporousbiomaterialstofullyeradicateplanktonicandadherentstaphylococcusaureus AT boelche simultaneousdeliveryofmultipleantibacterialagentsfromadditivelymanufacturedporousbiomaterialstofullyeradicateplanktonicandadherentstaphylococcusaureus AT vogelyhc simultaneousdeliveryofmultipleantibacterialagentsfromadditivelymanufacturedporousbiomaterialstofullyeradicateplanktonicandadherentstaphylococcusaureus AT vermondent simultaneousdeliveryofmultipleantibacterialagentsfromadditivelymanufacturedporousbiomaterialstofullyeradicateplanktonicandadherentstaphylococcusaureus AT henninkwe simultaneousdeliveryofmultipleantibacterialagentsfromadditivelymanufacturedporousbiomaterialstofullyeradicateplanktonicandadherentstaphylococcusaureus AT weinansh simultaneousdeliveryofmultipleantibacterialagentsfromadditivelymanufacturedporousbiomaterialstofullyeradicateplanktonicandadherentstaphylococcusaureus AT zadpooraa simultaneousdeliveryofmultipleantibacterialagentsfromadditivelymanufacturedporousbiomaterialstofullyeradicateplanktonicandadherentstaphylococcusaureus AT aminyavaris simultaneousdeliveryofmultipleantibacterialagentsfromadditivelymanufacturedporousbiomaterialstofullyeradicateplanktonicandadherentstaphylococcusaureus |