Table 2.
Materials | Synthesis Techniques (Precursor) |
Material Description (Morphology/Particle Size) | Antimicrobial Activity Test Methods | Antimicrobial Activity against Pathogenic Microorganisms | Refs. |
---|---|---|---|---|---|
ZnO materials | |||||
0D structured ZnO NPs | Hydrothermal method or room temperature synthesis (zinc nitrate hexahydrate; zinc sulfate; zinc acetate dihydrate) |
Spheres/12 nm, 25 nm; 30 nm, 88 nm, 142 nm, 212 nm, 307 nm | Turbidity | 6 mM, [Staphylococcus aureus] 30 nm: 10.11% growth; 88 nm: 54.34% growth; 142 nm: 78.12% growth; 212 nm: 79.79% growth; 307 nm: 96.67% growth, [Proteus vulgaris] 12 nm: 8.71% growth, [Salmonella typhimurium] 12 nm: 46.96% growth, [Shigella flexneri] 12 nm: 5.95% growth, [Bacillus cereus] 12 nm: 7.62% growth |
[16] |
Green method using Aloe vera leaf extract (zinc acetate dihydrate) |
|
Well diffusion, broth microdilution; MIC | MIC, [E. coli] ZnO-1, ZnO-2, and ZnO-3: 1562 μg/mL; [S. aureus] ZnO-1: 781 μg/mL, ZnO-2 and ZnO-3: 391 μg/mL; [B. subtilis] ZnO-1 and ZnO-2: 391 μg/mL; ZnO-3: 195 μg/mL |
[17] | |
Precipitation method (zinc acetate dihydrate) | Nanopyramids/~15.4 nm in segments | Colony counting, serial dilution; MIC | [Methicillin-resistant S. aureus (MRSA)] MIC, 333 μg/mL (3 log (CFU/mL) inhibition at 800 μg/mL) | [96] | |
Soft chemical synthesis (micrometric ZnO) | Spherical NP cluster/cluster-590 nm; NPs-63 nm | Colony counting | Antimicrobial activity value of log (control/sample), [E. coli] > 3.5; [S. aureus] > 3.5 |
[19] | |
1D structured ZnO NPs | Hydrothermal method (zinc acetate dihydrate) |
Hollow nanotubes/particle size ~500 nm in length; surface area 17.8 m2/g; average pore size, 278.6 nm | Disk diffusion; MIC | As-synthesized ZnO nanopowders, MIC, [Escherichia coli] 0.0585 mg/mL, [S. aureus] 0.234 mg/mL, [Pseudomonas aeruginosa] 0.234 mg/mL, [Bacillus subtilis] 0.938 mg/mL |
[54] |
Atomic layer deposition process over polymer template and template removal | Hollow nanotubes/length, ~5 μm; thickness, 59.5 nm; internal diameter, 178.2 nm | Colony counting | ZnO nanotubes at 1 wt% with acrylic polymer/extruded 32 μm-polyethylene (PE) substrate film coating [E. coli] 4.67 log reduction (cells/cm2), [S. aureus] 2.46 log reduction (cells/cm2) |
[55] | |
Precipitation method (zinc nitrate) | Nanorods/88.7 nm using 2-mercaptoethanol as a capping agent | Disk diffusion method, serial dilution; MIC | [Klebsiella pneumoniae] MIC, 40 μg/mL | [99] | |
Green method using Chlorella vulgaris culture supernatant (zinc acetate dihydrate) | Nanorods/crystal size, 3.4 nm; length-150 nm; width-21 nm (aspect ratio of length to width 7.14) | Microdilution; MIC | [E. coli, P. aeruginosa, S. aureus] MIC, 250 μg/mL (excluding Enterococcus faecalis: resistant to ZnO nanorods) |
[100] | |
Sol–gel method (zinc nitrate hexahydrate) | Nanorods/500 nm–1 μm | Disk diffusion | [Capping agent: ethylenediamine] E. coli-inhibition, Micrococcus luteus-no inhibition, [Capping agent: citric acid monohydrate] E. coli-no inhibition, B. subtilis-inhibition |
[101] | |
2D structured ZnO NPs | Not available (conventional products) |
|
Disk diffusion, broth dilution; MIC | ZnO-1, ZnO-2, ZnO -3, MIC (wt%), [E. coli] 0.12, 0.18, 2.30; [S. aureus] 0.25, 0.30, 3.40; [P. aeruginosa] 1.28, 4.68, 5.70; [Candida albicans] >8; >8; >8; [Aspergillus brasiliensis] nil, nil, nil |
[58] |
3D structured ZnO NP network | Sol–gel method (zinc acetylacetonate hydrate) | Spherical NP aggregate network/aggregates: ~3 μm; NPs: 48.3 nm | Colony counting; photocatalytic incubation | [E. coli] {Dual UV for 30 s} no particles-~approx. 2.8–3.0 log (CFU/mL), 0.05 mg/mL-no colonies detected | [18] |
ZnO NP mixtures | Green method using Butea monsoperma seed extract (zinc nitrate hexahydrate) | Mixtures/25 nm | Broth dilution; MIC | [P. aeruginosa (resistant to amikacin (30 μg), cefepime (30 μg), sparfloxacin (5 μg), piperacillin (100 μg), levofloxacin (5 μg), piperacilin-tazobactum (100/10 μg), imipenem (10 μg), tobramycin (10 μg), nitrofurantoin (300 μg), and ceftazidime (30 μg))] MIC, 1600 μg/mL; 1600–3200 μg/mL for isolates from patients |
[102] |
ZnO MPs | Flame transport synthesis (zinc microparticles) | Tetrapods/~30 μm | Plaque assay | [Herpes simplex virus type-2 (HSV-2)] ZnO tetrapod NP and HSV-2 cocktail for live virus vaccine | [95,103] |
Green method using starch (zinc acetate) | Self-assembled hollow microdonuts/1–2 μm | Disk diffusion | [Enterobacter aerogenes and Staphylococcus epidermidis] 0.5–5 mM | [104] | |
Combinations of ZnO materials with drugs | |||||
ZnO NPs with azithromycin, gentamicin, oxacillin, cefotaxime, cefuroxime, fosfomycin, chloramphenicol, and oxytetracycline | Green method using Ulva fasciata alga extract (zinc acetate dehydrate) |
Flakes/length, ~200 nm | Disk diffusion; MIC |
|
[20] |
ZnO with cephalexin nanohybrids | Ion exchange via sol–gel method (ZnO, and 2,4-chlorophenoxyacetic acid) | Squeezed ZnO crystals/not available | Disk diffusion; MIC | ZnO with cephalexin nanohybrids: MIC, [Aeromonas spp.] 1 mg/mL | [21] |
ZnO NPs with β-lactam antibiotics (ciprofloxacin and imipenem) | Not available (conventional product) | Not available | Disk diffusion; agar dilution; MIC | MIC
|
[79] |
ZnO NPs with ceftriaxone (CFX-ZnO NPs), ceftazidime (CFZ-ZnO NPs), and gentamicin (GTM-ZnO NPs) | Green method using Enterococcus faecalis culture supernatant (zinc sulfate) | Spheres/15.3–37 nm | Broth dilution; MIC |
|
[105] |
ZnO NPs with ampicillin/sulbactam | Milling method (zinc chloride) | Not available/25 nm | Disk diffusion; broth dilution; MIC | MIC,
|
[106] |
Combinations of ZnO materials with other metal oxide NPs / MPs, or metal doping | |||||
ZnO NPs with TiO2 NPs in 4A zeolite | Ion exchange process (zinc acetate dehydrate) |
Cubes/400–600 nm (NPs: spheres, ~50 nm) | Disk diffusion; MIC | MIC, [E. coli O157:H7] 1 mg/mL, [S. aureus] 2 mg/mL, [Pseudomonas fluorescens] 1 mg/mL, [Listeria Monocytogenes] 2 mg/mL |
[80] |
Ag-ZnO·mSiO2 composites | Precipitation of sodium water glass in zinc acetate solution (zinc acetate dihydrate) | Lamellar porous nanostructure with silver spots/not available (specific surface area, 250 m2/g) | Microdilution; MIC | MIC, [E. coli] 2.9 mg/cm3, [P. aeruginosa] 3.9 mg/cm3, [Streptococcus salivarius] 5.9 mg/cm3, [S. aureus] 5.9 mg/cm3, [C. albicans] 23.5 mg/cm3—synergistic | [81] |
ZnO-SiO2 composites | Solid state mixing (zinc acetate dihydrate) |
|
Broth microdilution; MIC | MIC, [S. aureus] 2 mg/mL (except for ZnO/S-S-20, C-A-10, or C-A-20, >2) as 0.228–0.632 mg/mL of ZnO NPs, [C. albicans] 1 or 2 mg/mL (except for ZnO/S-A-10 or S-S-10 >2) as 0.187–0.632 mg/mL of ZnO NPs | [115] |
CuZnO NPs on mesoporous silica SBA-3 | Co-condensation method (zinc nitrate) |
|
Colony counting; MIC | MIC, [E. coli] 25 mg/mL (CuZnO, 0.558 mg/mL), [S. aureus] 6.25 mg/mL (CuZnO, 0.139 mg/mL) | [117] |
ZnO MPs with TiO2 MPs | Sol–gel method (zinc chloride) |
|
Broth dilution; MIC; photocatalytic incubation under visible light irradiation | ZnO MPs (0.25%) with TiO2 MPs (1%): [E. coli] 76.8% growth inhibition, [Streptococcus pyogenes] 70.2% growth inhibition, [K. pneumoniae] 80.8% growth inhibition | [118] |
Combinations of ZnO materials with other biomaterials | |||||
Chitosan | |||||
Chitosan-ZnO NP-loaded gallic acid (C-ZnO@gal) films |
Hydrothermal method (zinc sulfate) |
|
Agar well diffusion | 0.5 mg/mL, [E. coli] 28 mm zone of inhibition, [B. subtilis] 25 mm zone of inhibition |
[28] |
ZnO NP-containing chitosan coating | Not available (conventional product: 2% w/v solution, 10–30 nm) |
|
Broth dilution; MIC | [E. coli O157:H7] ▪ Chitosan (2.5%, w/v): 2.5 log (CFU/g) reduction at 4 °C ▪ ZnO NP (1%, w/v)-containing chitosan (2.5%, w/v): 2.8 log (CFU/g) reduction at 4 °C |
[82] |
ZnO NP-containing chitosan/gelatin hybrid nanocomposite (nZnO-chitosan/gelatin) films | Green method using Cassia fistula fruit extract (zinc nitrate hexahydrate) |
|
Disk diffusion | [E. coli] ZnO NPs in films: 1%-10.5 mm zone of inhibition, 2%—10.5 mm zone of inhibition, 4%—10.7 mm zone of inhibition [S. aureus] not prominent compared to E. coli |
[91] |
3D porous ZnO NP-chitosan/silk/sericin scaffolds for wound dressing | Not available (conventional product: solution, ~35 nm) | Porous microstructures/not available (porosity ~86%; pore size 4–200 μm) |
Disk diffusion | 1.5 × 1.5 cm2, 2% (w/v) chitosan, 100 μL and 250 μL of ZnO NPs (40 wt% dispersion), [E. coli] 2–4.5 mm zone of growth inhibition, [S. aureus] 2.5–5.5 mm zone of growth inhibition |
[136] |
Chitosan-based ZnO nanocomposites | Co-precipitation (zinc acetate dihydrate) |
|
Disc diffusion | Zone of inhibition (mm), [K. pneumoniae] 13 mm (the highest) > [E. coli] > [P. aeruginosa] > [B. subtillis], [S. aureus], and [MRSA] 6 mm (the lowest) |
[137] |
Hydroxyapatite & alginate | |||||
Hydroxyapatite-biphasic ZnO NP/MP-embedded alginate beads | Precipitation (zinc nitrate) |
|
Agar diffusion; colony counting; MIC | 0.1 mg/mL, [E. coli] 56% inhibition, [P. aeruginosa] 65% inhibition, [S. aureus and S. epidermidis] 100% inhibition |
[83] |
Polyethylene glycol | |||||
Tungsten-doped polyethylene glycol-capped ZnO (W-PEG-ZnO) NPs | Electrochemical method (Zn electrodes) |
Near-spheres/~40.46 nm | Agar well diffusion | ▪ Ampicillin: 100 μg/μL [E. coli] 35 mm zone of inhibition, [B. cereus] 20 mm zone of inhibition ▪ W-PEG-ZnO NPs: [E. coli] 400–600 μg/μL, 5–6 mm zone of inhibition, [B. cereus] 300–600 μg/μL, 6–8 mm zone of inhibition |
[120] |
K-carrageenan, bacterial cellulose, propolis extract& curcumin | |||||
Biopolymer K-carrageenan wrapped ZnO (KC-ZnO) NPs | Precipitation (zinc acetate dehydrate) |
KC-ZnO NPs: ovals/97 nm | Disk diffusion; MIC | [MRSA] MIC, 7.50 μg/mL | [27] |
Bacterial cellulose-ZnO NP-propolis extract (BC-ZnO-propolis) films | Ultrasound (zinc acetate) |
|
Disk diffusion; MIC; photocatalytic incubation (254 nm, 30 min) | MIC, [E. coli] >1.89 mg/mL, [B. subtilis] 0.44 or <0.44 mg/mL, [C. albicans] >0.8, 1.3, 1.89, >1.89 mg/mL |
[121] |
Curcumin-loaded ZnO (C-ZnO) NPs | Sol–gel method (zinc nitrate hexahydrate) |
|
Well diffusion; colony counting | Zone of inhibition (mm), [E. coli] C-sZnO, 8.4; C-rZnO, 10.1; C-jZnO, 11.1; C-spZnO, 8.1; C-lpZnO, 9.8; C, 7.4 [S. epidermis] C-sZnO, 19.1; C-rZnO, 17.2; C-jZnO, 19.4; C-spZnO, 16.4; C-lpZnO, 20.1; C, 8.2 [S. aureus] C-sZnO, 15.4; C-rZnO, 16.6; C-jZnO, 13.4; C-spZnO, 15.2; C-lpZnO, 17.0; C, 8.1 [B. cereus] C-sZnO, 17.4; C-rZnO, 18.7; C-jZnO, 18.7; C-spZnO, 14.2; C-lpZnO, 14.2; C, 8.4 |
[124] |
Graphene, graphene oxide, & reduced graphene oxide | |||||
Graphene/ZnO nanocomposite films | Ion exchange process (zinc acetate) |
|
Microdilution; MIC | [Streptococcus mutans] MIC, 125 μg/mL | [84] |
Graphene/ZnO nanocomposite with curcumin (C-ZnO) | Ion exchange process (zinc acetate dihydrate) |
|
Agar diffusion; colony counting; microdilution; MIC | MIC,
|
[85] |
Graphene oxide (GO)/ZnO nanocomposite for wound care | Co-precipitation (zinc nitrate) |
▪ GO: smooth and wrinkled surface layers/not available▪ GO/ZnO nanocomposite: well incorporated and distributed ZnO NPs (0.1–0.4 M) on GO sheets forming agglomerates/not available | Disk diffusion, colony counting; dark (D) and visible light-irradiated (L) conditions | Zone of growth inhibition (mm), ▪ ZnO NPs (0.4 M) on GO sheets, 100 μg/mL [E. coli] GO-D, 11 mm; L, 11.5 mm; GO/ZnO (0.4 M)-D, 11 mm; L, 13 mm [P. aeruginosa] GO-D, 10 mm; L, 10.5 mm; GO/ZnO (0.4 M)-D, 10 mm; L, 13 mm [S. typhi] GO-D, 10.5 mm; L, 9 mm; GO/ZnO (0.4 M)-D, 11 mm; L, 11.5 mm [S. flexneri] GO-D, 8 mm; L, 10.6 mm; GO/ZnO (0.4 M)-D, 12 mm; L, 12.5 mm |
[86] |
GO/ZnO composites | Ion exchange process (zinc acetate dihydrate) |
|
Agar disk diffusion; MIC | [E. coli] MIC, 2 μg | [87] |
Reduced graphene oxide (rGO)/ZnO films | Sol–gel synthesis (zinc acetate dihydrate) |
|
Serial dilution; colony counting; MIC; photocatalytic incubation (UV at 365 nm) | [S. aureus] 1 wt% rGO >99% (>2-log) reduction |
[88] |
Cotton fabric | |||||
ZnO MPs-loaded chitosan-coated cotton fabrics | Precipitation (zinc chloride) |
Uniformly distributed dense microstructure of rods/not available | Disk diffusion | [E. coli] 2.5 cm zone of growth inhibition (ZnCl2 4%, chitosan 1–2%/1 g cotton fabric) | [126] |
Cotton-ZnO NP composites (C-nZnO) | Precipitation (zinc chloride) |
|
Disk diffusion; colony counting | nZnO amounts in C-nZnO: 2.2, 1.7, 4.9, 4.3, 11.1, 7.8, 22.2, and 16.7 wt% 9 mm in diameter, [E. coli] 97–100% growth reduction, [S. aureus] 96–98% growth reduction |
[127] |
ZnO NP-coated fabric | Green method using starch (zinc nitrate) |
|
Colony counting | 4.8 cm in diameter of fabric, [E. coli] 80% reduction [S. aureus] 99.99% reduction |
[129] |
ZnO quantum dots (QDs) | |||||
Different nanostructure-based ZnO QDs (ZnO QD-1–ZnO QD-14) | Sol–gel method (zinc acetate dihydrate) |
Nanorods, nanotubes, nanospheres, nanowhiskers, nanoflowers/not available | Agar well diffusion; agar dilution; MIC | MIC, [E. coli] ZnO QD-1: 25 mg/mL, [Enterobacter aerogenes] ZnO QD-4 and ZnO QD-6: 25 mg/mL, [K. pneumonia] ZnO QD-3 and ZnO QD-5: 12.5 mg/mL, [P. aeruginosa] ZnO QD-3 and ZnO QD-7: 12.5 mg/mL, [Bacillus anthracis] ZnO QD-2, ZnO QD-3 and ZnO QD-8: 6.25 mg/mL, [S. aureus] ZnO QD-8: 6.25 mg/mL, [L. monocytogenes] ZnO QD-6 and ZnO QD-7: 50 mg/mL, [E. faecalis] ZnO QD-2 and ZnO QD-7: 25 mg/mL, [B. cereus] ZnO QD-3 and ZnO QD-5: 12.5 mg/mL, [S. epidermidis] ZnO QD-8: 1.5 mg/mL |
[89] |
ZnO QDs | Green method using Eclipta alba leaf extract (zinc acetate dihydrate) |
Spheres/~6 nm | Agar diffusion | [E. coli] 15.69 mm zone of inhibition (1.6-fold increase compared to bulk zinc acetate at 5 mM) | [90] |
Antimicrobial peptide-based ZnO QDs containing vancomycin and methicillin (Van@ZnO-BSA-PEP-MPA; Met@ZnO-BSA-PEP-MPA) | Precipitation (zinc acetate) |
ZnO@BSA-PEP-MPA: spheres/104 nm | Broth dilution; MIC; in vivo diagnostics-4 × 108 CFU S. aureus for infection and Van@ZnO-BSA-PEP-MPA at 5.0 mg/kg for theranostics | MIC,
|
[141] |
Polyvinylpyrrolidone-capped ZnO (PVP-ZnO) QDs | Precipitation (zinc acetate hydrate) |
|
Agar diffusion; colony counting |
|
[142] |