Atomic Layer Deposition of Antibacterial Nanocoatings: A Review
Abstract
:1. Introduction
2. Methods
Literature Search
3. Results
3.1. Titanium Oxide
3.1.1. Photocatalytic Generation of ROS
3.1.2. Morphology and Topography of Surface
3.1.3. Thickness of the Coatings
3.1.4. Crystalline Structure of the Coatings
3.1.5. Precursors and ALD Temperature
3.1.6. Effect of Coatings on Different Strains
3.2. Doped TiO2 and Combined TiO2
3.3. Zinc Oxide
3.3.1. Mechanisms of ZnO Bactericidal Effect and Their Role
3.3.2. The Effect of Thickness
3.3.3. The Effect of the Deposition Temperature
3.3.4. The Effect of the Morphology, Topography, and Wettability
3.3.5. Effects on Various Types of Bacteria and Viruses
3.4. ZnO-Based Nanocomposites and Nanolaminates
3.5. Other Binary and More Complex Oxide Compounds
3.6. Silver and Other Metals
3.6.1. ALD of Silver Nanoparticles and Nanocoatings
3.6.2. ALD of Other Metallic Nanocoatings
4. Applications for ALD Antibacterial Coatings
4.1. Medical Implants
4.2. Antibacterial Textile and Personal Protective Equipment
4.3. Purification and Disinfection of Water and Air
4.4. Other Application
5. Analysis of the Results
5.1. Comparison of Different Antibacterial Coatings
5.2. Advantages, Disadvantages, and Perspectives of ALD
6. Conclusions
Supplementary Materials
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
Abbreviations
References
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Motivation | Support/Precursors | ALD Temperature/Thickness | Bacteria/Irradiation | Results | Ref. |
---|---|---|---|---|---|
Examine antibacterial coatings for purifying water. | Si/TiCl4/H2O | 100, 200, 300 °C/50 nm | E. coli/ UV irradiation | Increasing ALD temperature from 200 °C to 300 °C improves TiO2 photocatalytic activity but does not have an impact on antibacterial activity. E. coli survival: 200 °C–61%, 300 °C–66%. | [48] |
Study the effect of coatings with different morphology and structure on osteoblast, fibroblast functions, and bacterial activities. | Ti/TDMAT/H2O | 120, 160, 190 °C/100 nm | S. aureus, E. coli, MRSA | TiO2 inhibit adhesion and growth bacteria and fibroblast but improve osteoblasts adhesion and proliferation. The 160 °C sample (amorphous) showed the best antibacterial activity. An increase in nanoscale roughness and greater hydrophilicity contribute to increased protein adsorption, which may affect the cellular/bacterial activities. | [49] |
The study of photocatalytic processes in antibacterial activity TiO2. | Black Si and SiO2 nanopillars/(no data) | No data/50 nm | E. coli | The increase in the light absorption does not lead to an increase in ROS production. TiO2-coated nanopillars arrays made of SiO2 have 73% higher bactericidal efficacies than those made of Si. | [50] |
Study of the synergic effect present in mixed anatase/rutile TiO2 on antibacterial properties. | Rutile-TiO2 nanotubes (RTNT)/ TDMAT/H2O | 250 °C Annealing—450 °C 2 h/10 nm | E. coli/ UV light irradiation | A considerable increase in photocatalytic activity and ROS generation using RTNT coated with anatase-TiO2 compared to only rutile or anatase. A considerable increase in bactericidal activity using RTNT coated with A-TiO2 compared to single R or A-TiO2 nanotubes. | [45] |
Examine surface coating of nanoporous Al2O3 for controlled pore size reduction. | Porous Al2O3 membranes/TiCl4/H2O | 300 °C/4.3 and 8.6 nm | S. aureus, E. coli, UV irradiation | The 20 nm pore size TiO2-coated nanoporous alumina membrane inhibited microbial adhesion while the 100 nm pore size TiO2-coated membrane did not. | [51] |
Examine the efficiency of a bacteria-resistant coating for the PDMS cochlear implants. | PDMS 1/TDMAT/O2 plasma | 100 °C/(10–40 nm) | E. coli | TiO2-coated surfaces save the integrity of polymeric materials and reduce E. coli colonization and biofilm formation with protein quantity on ALD- and lymphoproliferative diseases (LPD) treated samples being reduced by 44 and 41%. Confocal laser scanning microscopy—biofilm reduction of 91% for ALD-coated surfaces. | [52] |
Studies of antibacterial properties of TiO2 deposited on polymers used for catheters and contact lenses. | PU 2 and PDMS/ TiCl4/H2O | 80 °C/50–200 nm | Candida albicans UV and without UV | TiO2 suppressed the yeast hyphal transition of C. albicans onto PU; however, a high adhesion of C. albicans was observed. For PDMS + TiO2, the yeast adhesion did not change, as observed in the control. After UV treatment, TiO2+PDMS had better reduction in the colony-forming unit CFU (up to 59.5%) compare to the uncoated PDMS, while no difference was observed in TiO2-covered PU. | [29] |
Improve the surface characteristics of denture PMMA. | PMMA 3/TDMAT/O3 | 65 °C/30 nm | Candida albicans | C. albicans reduction reached 63% to 77% for the attachment test and 56% for biofilm formation. | [53] |
Support/ALD Conditions | Characteristics | Bacteria | Results | Ref. |
---|---|---|---|---|
TiO2 nanotubes 10–84 nm/25 cycles of plasma enhanced atomic layer deposition (PEALD) Ag(fod)(PEt3) 1 +H2 (120 °C). | 7.8–9.2 nm dispersed Ag particles and dense Ag layer | S. aureus | Low level of Ag+ releasing the sample with the smallest nanotube diameter and a continuous layer of Ag showed the best bactericidal results. | [102] |
3d Ti scaffolds/direct liquid injection of 0.1 M (hfac)Ag(1,5-COD) 2 in toluene and propan-1-ol. 500 ALD cycles (125 °C). | Effective layer—13 nm (NPs 40–90 nm diameter) | S. aureus (MRSA) S. epidermidis. | On bare titanium scaffolds, S. epidermidis growth was slow but on Ag-coated there were significant further reductions (two orders of inhibition) in both bacterial recovery and biofilm formation. MRSA growth was similarly slow on bare titanium and not further affected by Ag coating. | [122] |
3d Ti scaffolds/direct liquid injection 0.1M (hfac)Ag(1,5-COD) in toluene and propan-1-ol. 500 ALD cycles (125 °C). | Average NPs 49 nm in diameter | In vivo—implants in rat tibial defects | No effect of Ag on bone formation and osseointegration after 2–12 weeks of implantation. Ag is a part of less toxic Ag2S within the newly formed bone tissue adjacent to the implant surface. | [27] |
Ti/ALD TiO2 (TiCl4 + H2O) + Ag (Ag(fod)(PEt3) + H2). | 20–28 nm on Si 16–30 nm on Ti | S. aureus | The ALD combination of TiO2 + Ag is significantly more active against S. aureus than pure TiO2 and Ag. | [57] |
N95 medical mask (PP, polyester)/Ag(fod)(PEt3) + (CH3)2NH*BH3. | 16 nm | S. aureus | A 76% reduction in S. aureus CFU was observed after 24 h. At an early stage (2 h), Ag had no bactericidal effect. | [123] |
Characteristics | TiO2 | Doped TiO2 | ZnO | Ag | ZrO2 | Fe2O3 | Al2O3 |
---|---|---|---|---|---|---|---|
Antibacterial efficacy | + | ++ | +++ | +++ | 0 | + | 0 |
Biocompatibility | +++ | ++ | + | + | ++ | + | + |
ALD temperature | From 65 °C | From 65 °C | From RT | 120–160 °C | ~200 °C | ~180 °C | From RT |
Growth rate, uniformity, and conformality | ++ | ++ | +++ | + | ++ | ++ | +++ |
Morphology of the coating | Dense coating | Dense coating | Dense nanocrystalline coating | NPs | Dense coating | Dense coating | Dense coating |
Stability in aqueous environment | +++ | ++ | + | + | +++ | + | +++ |
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Nazarov, D.; Kozlova, L.; Rogacheva, E.; Kraeva, L.; Maximov, M. Atomic Layer Deposition of Antibacterial Nanocoatings: A Review. Antibiotics 2023, 12, 1656. https://doi.org/10.3390/antibiotics12121656
Nazarov D, Kozlova L, Rogacheva E, Kraeva L, Maximov M. Atomic Layer Deposition of Antibacterial Nanocoatings: A Review. Antibiotics. 2023; 12(12):1656. https://doi.org/10.3390/antibiotics12121656
Chicago/Turabian StyleNazarov, Denis, Lada Kozlova, Elizaveta Rogacheva, Ludmila Kraeva, and Maxim Maximov. 2023. "Atomic Layer Deposition of Antibacterial Nanocoatings: A Review" Antibiotics 12, no. 12: 1656. https://doi.org/10.3390/antibiotics12121656
APA StyleNazarov, D., Kozlova, L., Rogacheva, E., Kraeva, L., & Maximov, M. (2023). Atomic Layer Deposition of Antibacterial Nanocoatings: A Review. Antibiotics, 12(12), 1656. https://doi.org/10.3390/antibiotics12121656