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Bactericidal effects of nanopatterns: A systematic review
Khashayar Modaresifar1, Sara Azizian1, Mahya Ganjian1
1Department of Biomechanical Engineering, Faculty of Mechanical, Maritime, and Materials Engineering, Delft University of Technology, Mekelweg 2, 2628CD Delft, The Netherlands.
Surface nanopatterns kill bacteria without antibiotics. This review identifies optimal design parameters like height, diameter, and spacing for effective bactericidal behavior and cytocompatibility.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Microbiology
Background:
- Antibiotic resistance necessitates novel antibacterial strategies.
- Surface nanopatterns offer a physical method to combat bacterial infections.
- Understanding nanopattern design is crucial for efficacy.
Purpose of the Study:
- To systematically review evidence on surface nanopattern design parameters and their bactericidal behavior.
- To identify optimal dimensions for nanopatterns to kill bacteria.
- To assess the cytocompatibility of bactericidal nanopatterns.
Main Methods:
- Systematic literature review of 46 studies.
- Inclusion criteria: bactericidal behavior of nanopatterns with known design parameters, absence of antibacterial agents.
- Assessment of cytocompatibility in 12 studies.
Main Results:
- Natural and synthetic nanopatterns show bactericidal behavior across various designs.
- Optimal ranges identified: heights 100-1000 nm, diameters 10-300 nm, interspacings <500 nm.
- Nanopillars most common; optimal ranges: heights 100-900 nm, diameters 20-207 nm, interspacings 9-380 nm.
- 11 of 12 cytocompatibility studies showed no adverse effects, except for high aspect ratio nanopatterns.
Conclusions:
- Surface nanopatterns are effective antibacterial agents without antibiotics.
- Key design parameters (height, diameter, interspacing) influence bactericidal efficiency.
- Nanopillars show promise within specific dimensional ranges.
- Bactericidal nanopatterns are generally cytocompatible, with exceptions for high aspect ratios.
- Further research should consider bacterial surface affinity, cell size, and EPS for enhanced killing mechanisms.
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