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Antimicrobial Peptides in Biomedical Device Manufacturing. / Riool, Martijn; de Breij, Anna; Drijfhout, Jan W. et al.

In: Frontiers in chemistry, Vol. 5, 2017, p. 63.

Research output: Contribution to journalReview articleAcademicpeer-review

Harvard

Riool, M, de Breij, A, Drijfhout, JW, Nibbering, PH & Zaat, SAJ 2017, 'Antimicrobial Peptides in Biomedical Device Manufacturing', Frontiers in chemistry, vol. 5, pp. 63. https://doi.org/10.3389/fchem.2017.00063

APA

Riool, M., de Breij, A., Drijfhout, J. W., Nibbering, P. H., & Zaat, S. A. J. (2017). Antimicrobial Peptides in Biomedical Device Manufacturing. Frontiers in chemistry, 5, 63. https://doi.org/10.3389/fchem.2017.00063

Vancouver

Riool M, de Breij A, Drijfhout JW, Nibbering PH, Zaat SAJ. Antimicrobial Peptides in Biomedical Device Manufacturing. Frontiers in chemistry. 2017;5:63. doi: 10.3389/fchem.2017.00063

Author

Riool, Martijn ; de Breij, Anna ; Drijfhout, Jan W. et al. / Antimicrobial Peptides in Biomedical Device Manufacturing. In: Frontiers in chemistry. 2017 ; Vol. 5. pp. 63.

BibTeX

@article{6357286966ef4dd0b65ac3f801d205eb,
title = "Antimicrobial Peptides in Biomedical Device Manufacturing",
abstract = "Over the past decades the use of medical devices, such as catheters, artificial heart valves, prosthetic joints, and other implants, has grown significantly. Despite continuous improvements in device design, surgical procedures, and wound care, biomaterial-associated infections (BAI) are still a major problem in modern medicine. Conventional antibiotic treatment often fails due to the low levels of antibiotic at the site of infection. The presence of biofilms on the biomaterial and/or the multidrug-resistant phenotype of the bacteria further impair the efficacy of antibiotic treatment. Removal of the biomaterial is then the last option to control the infection. Clearly, there is a pressing need for alternative strategies to prevent and treat BAI. Synthetic antimicrobial peptides (AMPs) are considered promising candidates as they are active against a broad spectrum of (antibiotic-resistant) planktonic bacteria and biofilms. Moreover, bacteria are less likely to develop resistance to these rapidly-acting peptides. In this review we highlight the four main strategies, three of which applying AMPs, in biomedical device manufacturing to prevent BAI. The first involves modification of the physicochemical characteristics of the surface of implants. Immobilization of AMPs on surfaces of medical devices with a variety of chemical techniques is essential in the second strategy. The main disadvantage of these two strategies relates to the limited antibacterial effect in the tissue surrounding the implant. This limitation is addressed by the third strategy that releases AMPs from a coating in a controlled fashion. Lastly, AMPs can be integrated in the design and manufacturing of additively manufactured/3D-printed implants, owing to the physicochemical characteristics of the implant material and the versatile manufacturing technologies compatible with antimicrobials incorporation. These novel technologies utilizing AMPs will contribute to development of novel and safe antimicrobial medical devices, reducing complications and associated costs of device infection",
author = "Martijn Riool and {de Breij}, Anna and Drijfhout, {Jan W.} and Nibbering, {Peter H.} and Zaat, {Sebastian A. J.}",
year = "2017",
doi = "10.3389/fchem.2017.00063",
language = "English",
volume = "5",
pages = "63",
journal = "Frontiers in chemistry",
issn = "2296-2646",
publisher = "Frontiers Media S.A.",

}

RIS

TY - JOUR

T1 - Antimicrobial Peptides in Biomedical Device Manufacturing

AU - Riool, Martijn

AU - de Breij, Anna

AU - Drijfhout, Jan W.

AU - Nibbering, Peter H.

AU - Zaat, Sebastian A. J.

PY - 2017

Y1 - 2017

N2 - Over the past decades the use of medical devices, such as catheters, artificial heart valves, prosthetic joints, and other implants, has grown significantly. Despite continuous improvements in device design, surgical procedures, and wound care, biomaterial-associated infections (BAI) are still a major problem in modern medicine. Conventional antibiotic treatment often fails due to the low levels of antibiotic at the site of infection. The presence of biofilms on the biomaterial and/or the multidrug-resistant phenotype of the bacteria further impair the efficacy of antibiotic treatment. Removal of the biomaterial is then the last option to control the infection. Clearly, there is a pressing need for alternative strategies to prevent and treat BAI. Synthetic antimicrobial peptides (AMPs) are considered promising candidates as they are active against a broad spectrum of (antibiotic-resistant) planktonic bacteria and biofilms. Moreover, bacteria are less likely to develop resistance to these rapidly-acting peptides. In this review we highlight the four main strategies, three of which applying AMPs, in biomedical device manufacturing to prevent BAI. The first involves modification of the physicochemical characteristics of the surface of implants. Immobilization of AMPs on surfaces of medical devices with a variety of chemical techniques is essential in the second strategy. The main disadvantage of these two strategies relates to the limited antibacterial effect in the tissue surrounding the implant. This limitation is addressed by the third strategy that releases AMPs from a coating in a controlled fashion. Lastly, AMPs can be integrated in the design and manufacturing of additively manufactured/3D-printed implants, owing to the physicochemical characteristics of the implant material and the versatile manufacturing technologies compatible with antimicrobials incorporation. These novel technologies utilizing AMPs will contribute to development of novel and safe antimicrobial medical devices, reducing complications and associated costs of device infection

AB - Over the past decades the use of medical devices, such as catheters, artificial heart valves, prosthetic joints, and other implants, has grown significantly. Despite continuous improvements in device design, surgical procedures, and wound care, biomaterial-associated infections (BAI) are still a major problem in modern medicine. Conventional antibiotic treatment often fails due to the low levels of antibiotic at the site of infection. The presence of biofilms on the biomaterial and/or the multidrug-resistant phenotype of the bacteria further impair the efficacy of antibiotic treatment. Removal of the biomaterial is then the last option to control the infection. Clearly, there is a pressing need for alternative strategies to prevent and treat BAI. Synthetic antimicrobial peptides (AMPs) are considered promising candidates as they are active against a broad spectrum of (antibiotic-resistant) planktonic bacteria and biofilms. Moreover, bacteria are less likely to develop resistance to these rapidly-acting peptides. In this review we highlight the four main strategies, three of which applying AMPs, in biomedical device manufacturing to prevent BAI. The first involves modification of the physicochemical characteristics of the surface of implants. Immobilization of AMPs on surfaces of medical devices with a variety of chemical techniques is essential in the second strategy. The main disadvantage of these two strategies relates to the limited antibacterial effect in the tissue surrounding the implant. This limitation is addressed by the third strategy that releases AMPs from a coating in a controlled fashion. Lastly, AMPs can be integrated in the design and manufacturing of additively manufactured/3D-printed implants, owing to the physicochemical characteristics of the implant material and the versatile manufacturing technologies compatible with antimicrobials incorporation. These novel technologies utilizing AMPs will contribute to development of novel and safe antimicrobial medical devices, reducing complications and associated costs of device infection

U2 - 10.3389/fchem.2017.00063

DO - 10.3389/fchem.2017.00063

M3 - Review article

C2 - 28971093

VL - 5

SP - 63

JO - Frontiers in chemistry

JF - Frontiers in chemistry

SN - 2296-2646

ER -

ID: 4066095