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Review

Iron Oxide Nanoparticles as Promising Antibacterial Agents of New Generation

by
Tian-Guang Zhang
* and
Chao-Yu Miao
*
Department of Pharmacology, Second Military Medical University/Naval Medical University, Shanghai 200433, China
*
Authors to whom correspondence should be addressed.
Nanomaterials 2024, 14(15), 1311; https://doi.org/10.3390/nano14151311
Submission received: 5 June 2024 / Revised: 27 July 2024 / Accepted: 1 August 2024 / Published: 3 August 2024
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Abstract

:
Antimicrobial resistance (AMR) is growing into a major public health crisis worldwide. The reducing alternatives to conventional agents starve for novel antimicrobial agents. Due to their unique magnetic properties and excellent biocompatibility, iron oxide nanoparticles (IONPs) are the most preferable nanomaterials in biomedicine, including antibacterial therapy, primarily through reactive oxygen species (ROS) production. IONP characteristics, including their size, shape, surface charge, and superparamagnetism, influence their biodistribution and antibacterial activity. External magnetic fields, foreign metal doping, and surface, size, and shape modification improve the antibacterial effect of IONPs. Despite a few disadvantages, IONPs are expected to be promising antibacterial agents of a new generation.

1. Introduction

AMR is growing into a major public health crisis worldwide and has been prioritized by the World Health Organization (WHO) as one of the top 10 global public health threats to humanity [1,2]. Without proactive solutions, it is estimated that global deaths due to AMR could reach up to 10 million annually by 2050 [3]. The increasing AMR and the reducing alternatives to conventional agents prompt the development of novel strategies to treat microbial diseases. Nanoparticles have received significant attention in medical sciences over the past decade due to their unique physicochemical properties [4,5]. Metal-based nanoparticles are among the most promising novel antimicrobial agents because of their strong antimicrobial activity [6,7,8,9]. Not only are some of the mechanisms of action they use different from those of traditional agents, but they also target multiple biomolecules, delaying the development of resistant strains [6,9].
IONPs are the most preferable nanomaterials in biomedicine, primarily due to their relative safety and magnetic properties [10]. The major forms of IONPs are magnetite (Fe3O4) and its oxidized forms, maghemite (γ-Fe2O3) and hematite (α-Fe2O3). Superparamagnetic iron oxide nanoparticles (Fe3O4 and γ-Fe2O3) can be used in an increasing number of biomedical applications, including but not limited to targeted drug delivery, magnetic resonance imaging (MIR), and magnetic hyperthermia, depending on their advantages such as an ability to be guided to a selected location by an external magnetic field, magnetic resonance imaging, and the generation of heat in an alternating magnetic field [11]. In 1957, the potential of IONPs for the heating of tumor tissue under an alternating magnetic field was examined for the first time [12], and magnetic hyperthermia was invented in 1993 [13]. In 1960, the concept of magnetic targeting was proposed and magnetic NPs are successfully accumulated in the body by magnetic field [14]. In 1996, the first phase I clinical trial of magnetic drug targeting using IONPs was conducted on patients bearing cancer [15]. Also occurring in 1996, the United States Food and Drug Administration (FDA) approved the first contrast agent based on IONPs [16]. Though magnetic hyperthermia was in the development stage, the FDA approved the first iron-replacement agent for the treatment of iron deficiency anemia in 1992 [17].
Iron is an essential element for most microorganisms. Bacteria also have an obligate requirement for iron to support their growth and survival. However, iron has double-edged sword effects on bacteria. High levels of iron are detrimental to bacteria. Bacteria have evolved a variety of mechanisms to maintain iron homeostasis, which not only allow them to survive under iron-restricted conditions but also protect them from iron-induced free radical damage under iron-rich conditions [18,19]. IONPs can result in cell iron overload. Thus, IONPs have also exhibited great antimicrobial activity against microorganisms, including bacteria, fungi, and viruses [8].
In this review, focusing on the antibacterial properties of IONPs, we introduce their potential mechanisms of action against pathogenic bacteria, their structure, the main factors influencing their antibacterial activity and biodistribution, and their biocompatibility. Additionally, we point out the disadvantages of IONPs and propose approaches for enhancing their antibacterial effect.

2. Antibacterial Potential Mechanisms of IONPs

Two main mechanisms are involved in the antibacterial action of IONPs, including damage to the cell wall and cell membrane through an electrostatic and van der Waals interaction and oxidative stress by ROS formation (Figure 1).
Bacterial membranes contain highly electronegative chemical groups that serve as the binding sites of metal cations [20]. Metal oxides promote adhesion to the surfaces of negatively charged bacteria, primarily due to their positive charge [21]. IONPs can adhere to the cell wall and cell membrane of bacteria by the electrostatic and van der Waals interaction [22]. Then, IONPs form clusters on the bacterial surface and cause cell wall and cell membrane disruption, leading to leakage of bacterial content [23].
The most important mechanism of antibacterial effects of IONPs is the induction of oxidative stress by the production of ROS such as superoxide anion, hydroxyl radical and nonradical hydrogen peroxide through Fenton or Fenton-like reactions [24]. After internalization in bacteria, iron ions are released from IONPs and react with hydrogen peroxide to produce ROS, which may directly damage DNA, lipids, and protein, resulting in the accumulation of oxidative injury and thus bacterial death [25].
The Fenton reaction occurs when hydrogen peroxide is converted into a hydroxyl free radical via a Fe2+-catalyzed process, and Fe2+ is an accelerator for this reaction. Fenton oxidants (such as hydroxyl radicals) are generated in the cells of Escherichia coli exposed to bactericidal antibiotics [26], suggesting that the Fenton reaction occurs in bacteria. IONPs can act as a source of ferrous ions and serve as the role of catalysts [27]. A recent study evaluated the antibacterial activity of superparamagnetic iron oxide nanoparticles (SPIONs), ferrous and ferric ions against Staphylococcus aureus and Escherichia coli [28]. Under aerobic conditions, ferrous ions showed the strongest inhibitory effect against the growth of both stains. In fact, the antimicrobial effect of ferric ions depends on their conversion to ferrous ions by bacteria [29]. As the SPIONs showed less ROS production and antibacterial activity than ferrous, it could be concluded that similar to ferrous ions, the main mechanism of antibacterial effects for SPIONs was ROS generation.

3. Structure of IONPs

Due to their high surface energies from the great surface-to-volume ratio, bare IONPs have a high tendency to aggregate into large particles to reduce the energy of the surface, resulting in a loss of magnetism. Moreover, due to the high chemical activity of their surface, bare IONPs are easily oxidized, causing a loss of magnetism. Therefore, coating IONPs is essential to make them stable and biocompatible. Organic and inorganic materials can function as a coating for IONPs. The core–shell structure is typical for IONPs. In this structure, the iron oxide core was encapsulated in an inorganic or organic coating, which renders the particle stable.
Organic compounds have good biodegradability and biocompatibility and can provide functional groups such as carboxyl, hydroxyl, thiol, and amino groups. These groups not only possess strong binding affinity towards IONPs but also enable linkage with active bio-substances such as drugs and antibodies for bio-applications. Organic compounds include small-molecule organic and polymeric-coating materials. Oleic acid and trisodium citrate can stabilize nanoparticles mainly by steric repulsive forces to balance the magnetic and van der Waals attractive forces [30], thereby producing highly uniform IONPs. 2,3-Dimercaptosuccinic acid (DMSA), with two carboxyl groups and two sulfhydryl groups, is another typical organic surface-coating compound of IONPs [31]. The DMSA binds to the IONP surface through its carboxyl groups and strengthens the nanocrystal stability. The remaining carboxylic acid groups supply the surface with a negative charge, which makes IONPs hydrophilic and is easy for further conjugation of other bio-substances. In contrast to most small molecules, polymers bind to nanoparticles by multiple groups, contributing to stronger steric repulsive forces. Due to the excellent colloidal stability of IONPs, polymeric-coating materials are the most used in IONPs. Natural and synthetic polymers such as polyethylene glycol (PEG) and chitosan are used to coat IONPs. PEG is a hydrophilic, uncharged polymer whose biocompatibility has been recognized by the FDA [32,33]. The only disadvantage of PEG is that it is not easily biodegraded under biological conditions [34]. Chitosan is a positively charged, hydrophilic polymer with good biocompatibility and biodegradability [35,36]. The positive charge can drive the chitosan-based nanoparticles to the negatively charged cell membrane. Owing to the cell adhesion and positive charge, chitosan is a frequent choice for drug delivery [37]. Furthermore, chitosan has a broad antimicrobial spectrum and is susceptible to a variety of Gram-negative and Gram-positive bacteria [35].
Inorganic compounds such as SiO2, gold (Au), and silver(Ag) are able to increase the antioxidant properties of IONPs [38]. Silica is one of the extensively used coating materials due to its hydrophilicity, biocompatibility, and ability to prevent nanoparticle aggregation [39]. The negatively charged surface of silica, derived from the deprotonation of silanol groups, stabilizes the IONPs coated in silica by electrostatic repulsive forces. In addition, the abundant silanol groups of the silica can be easily activated and offer perfect anchorages for various functional groups [40]. Coating IONPs with melt provides a relatively inert layer with increased biocompatible and stability [41,42]. Similar to the gold coating, the electron transfer between silver and IONPs creates a positively charged silver coating, allowing the conjugation of different antibiotics to the silver-decorated IONPs by electrostatic interaction [43,44].

4. Main Factors Influencing the Antibacterial Activity of IONPs

The unique physicochemical properties of IONPs have a profound effect on antibacterial activity. The size, shape, and surface charge of IONPs are some of the main factors determining the antibacterial activity.
Size effects on the adsorption of α-Fe2O3 nanoparticles were studied in Escherichia coli. Adsorption of large α-Fe2O3 nanoparticles (76 and 96 nm) on Escherichia coli cells, which took 30–40 min, reached equilibrium faster than small nanoparticles, which took approximately 60–90 min [45]. However, the size of nanoparticles is inversely proportional to their bacterial activity. Small Fe2O3 nanoparticles tend to be more toxic than large nanoparticles for Pseudomonas putida because small nanoparticles have a relatively larger surface area to volume ratio than large nanoparticles, resulting in a great increase in the production of ROS [46,47]. Another study also showed that small-size Zero-valent iron nanoparticles with an average diameter (~35 nm) could rapidly inactivate Escherichia coli [48].
Various types of nanostructures of IONPs have been prepared, such as nanosphere, nanorod, nanowire, nanocrystal, and so on [49]. Sphere-shaped iron oxide nanoparticles and rod-shaped iron oxide nanoparticles were found to show good antibacterial activity [50]. Rod-shaped IONPs are shown to be more toxic than sphere-shaped IONPs [51]. This is because, unlike spherical nanoparticles, nonspherical particles such as rod-shaped nanoparticles can increase the propensity of nanoparticle–cell wall contact and potential penetration through the cell wall [52].
Positively charged IONPs have been shown to have higher antimicrobial activity than negatively charged ones, as the negative charge of the bacterial cell wall more easily electrostatically attracts the positively charged IONPs [53]. Due to the increased negative net charge of the outer membrane as a result of their composition, Gram-negative bacteria interact more with positively charged IONPs than Gram-positive bacteria, which lack a cell envelope structure [6]. A study explored the antibacterial properties of both negatively charged IONPs and positively charged IONPs against Gram-positive Bacillus subtilis and Gram-negative Escherichia coli [54]. The experiments showed higher antimicrobial activity of positively charged IONPs than negatively charged IONPs, and positively charged IONPs are more toxic to Escherichia coli than Bacillus subtilis. In addition, positively charged and neutral IONPs showed higher toxicity on Streptococcus mutans biofilms in comparison with their negatively charged counterparts, highlighting the effect of the surface charge of IONPs on antibiofilm activity [55].

5. Main Factors Influencing the Biodistribution of IONPs

In addition to the ability to be directed to the desired tissues and organs by an external magnetic field, the size, shape, and surface charge of IONPs also influence their biodistribution in different organs (Figure 2 and Table 1). Intravenously injected IONPs are mainly accumulated and cleared in the liver and spleen by mononuclear phagocytic system (MPS) such as hepatic Kupffer cells and splenic macrophages [56,57]. For spherical IONPs, large-sized nanoparticles (>100 nm) accumulate readily within the liver and spleen, whereas small-sized nanoparticles (<15 nm) are eliminated by the kidneys [58].
Size is one of the primary factors determining the biodistribution of nanoparticles; however, shape is also as important. Discoidal particles favor their interaction with vessel–wall due to tumbling and oscillatory effects as well as more binding and contact points with the cell wall, compared with spherical particles [52]. For nanoparticles in the range of 20–150 nm, discoidal particles have been shown to accumulate more easily in the lung, liver, and spleen than spherical particles [52]. However, nanoparticles with a large length-to-width aspect ratio may increase their in vivo blood circulation time, owing to the tendency to align with blood flow and slower macrophage internalization [59,60]. For example, nanotube-shaped magnetic iron oxide nanoworms prolonged blood circulation times over their spherical counterparts [61].
The surface of IONPs is rapidly covered by blood plasma proteins in vivo after injection. The surface charge affects protein adsorption on the IONP surface and their MPS elimination. Adsorption of plasma proteins on the IONPs increases the size andthus MPS elimination [62]. Positively charged IONPs have a higher affinity to plasma proteins and show faster blood clearance in comparison with negatively charged IONPs [63,64]. Nanoparticles with a neutral or negative surface charge have been shown to have a longer circulation time due to a reduction in the adsorption of serum proteins [65]. Furthermore, negatively charged IONPs show a much lower affinity with cell membranes and less internalization due to the repulsive interactions with cell membranes [66]. Positively charged particles, such as positive charge IONPs, are more easily bound to macrophages in the lung, liver, and spleen, whereas neutral and negatively charged nanoparticles are less likely to accumulate in these organs [52,67].
Table 1. Antibacterial properties of IONPs.
Table 1. Antibacterial properties of IONPs.
TypeSize
(nm)		ShapeSurface
Charge		MIC
(µg/mL)		MBC
(µg/mL)		BacteriaRef.
Chitosan-Fe3O410–20SphericalPositiveNR
NR		NR
NR		E. coli
B. subtilis		[54]
PVA-Fe2O3/Fe3O49 ± 4SphericalNegativeNRNRS. aureus[68]
Amine-Fe3O46–15SphericalNegativeNR
NR		NR
NR		S. aureus
E. coli		[69]

Arg-Fe3O46–15SphericalNegativeNRNRS. aureus
APTMS -Fe3O46–15SphericalPositive125
125		NR
NR		S. aureus
E. coli
Oleic acid-Fe3O46–15SphericalNegative31
63		NR
NR		S. aureus
E. coli
Fe3O4 @PEG-Ag20–25SphericalNR16
16		32
32		E. coli
S. aureus		[70]
Fe3O4@Ag60 ± 20SphericalNR≥70
≥60
≥70		NR
NR
NR		E. coli
S. epidermidis
B. subtilis		[71]
CES-Fe3O413.8 ± 2.1SphericalNegativeNR
NR		NR
NR		S. aureus
S epidermidis		[72]
APTES-Fe3O417.8 ± 2.6SphericalPositiveNR
NR		NR
NR		S. aureus
S epidermidis
Fe3O413.7 ± 2.1SphericalPositiveNR
NR		NR
NR		S. aureus
S epidermidis
TEPSA-Fe3O412.1 ± 0.5SphericalNegativeNRNR [55]
TPED-Fe3O411.4 ± 0.4SphericalPositiveNRNRS. mutans Biofilm
Fe3O410.1 ± 0.6SphericalPositiveNRNR
Fe3O4@APTES17SphericalPositiveNRNRB. subtilis biofilm[73]
Fe2O335.16 ± 1.47SphericalNRNR
NR
NR
NR		65 ± 1.5
120 ± 2.3
80 ± 1.5
78 ± 1.4		E. coli
P. aeruginosa
S. aureus
B. subtilis		[74]
α-Fe2O320–30SphericalPositive>150
>150		NR
NR		V. cholerae
E. coli		[75]
CEL/γ-Fe2O3/Ag15–20 NRNR512
1024		1024
1024		S. aureus
E. coli		[76]
FeO20–80RodNegativeNRNRE. coli
K. pneumoniae
S. aureus		[77]
MIC: minimum inhibitory concentration; MBC: minimum bactericidal concentration; NR: not reported; Ref.: reference; PVA: polyvinyl alcohol; APTMS: amino-propyl trimethoxy silane; CES: carboxyethylsilanetriol; APTES: 3-aminopropyltriethoxysilane; TEPSA: 3-(triethoxysilyl) propylsuccinic anhydride; TPED: N-[3-(trimethoxysilyl)propyl] ethylenediamine; APTES: 3-aminopropyltriethoxy silane; CEL: cellulose.

6. Biocompatibility of IONPs

IONPs present low toxicity in the human body. After internalization in eukaryotic cells, the IONPs are presumably degraded into iron ions in the lysosomes, and then these iron ions are released to the cytoplasm [46]. These iron ions are either incorporated in hemoglobin in red blood cells or eliminated from the body through the kidneys [78]. Due to their broad safety margin, several IONPs have been approved by the FDA for clinical application as imaging contrast agents and iron-replacement agents, as mentioned above. Among several other metal oxide nanoparticles, IONPs display an acceptable safety profile and no or low cytotoxicity [79]. Cytotoxicity tests for human glia, breast cancer, and normal cell lines demonstrated that Fe3O4 nanoparticles showed almost nontoxicity at doses of <10 μg/mL [80]. No clinically significant side effects have been reported for dextran-coated IONPs (e.g., Ferumoxytol) by intravenous injection and silica-coated IONPs (e.g., Ferumoxsil) by oral administration according to the standard pharmacological tests [81,82].

7. Disadvantages of IONPs

For metal oxide nanoparticles, the antimicrobial action of IONPs is relatively weak [22]. The inhibitory action of Fe2O3 nanoparticles on both Gram-negative Escherichia coli and Pseudomonas aeruginosa and Gram-positive Staphylococcus aureus and Bacillus subtilis are less effective than ZnO or CuO nanoparticles [74]. There was even a study that showed that IONPs could promote the growth of Pseudomonas aeruginosa grown in iron-deficient media due to an exogenous iron source for the bacteria [83]. In addition, the non-specificity of the antimicrobial action of IONPs on pathogens and symbiotic microbes can be detrimental to the host. IONPs may inhibit symbiotic microbes within the gastrointestinal tract, which provide many benefits to the host, such as the promotion of host immunity.
Biosafety is important when applying IONPs in biomedical applications. IONPs have bacteriostatic and bactericidal activities, whereas excess iron can be lethal to not only bacterial cells but also eukaryotic cells. Most nanotoxicities from IONPs derive from the aforementioned production of ROS from the nanoparticle surface or iron ions release [33]. In spite of low cytotoxicity, some IONPs have also been reported to cause toxic effects related to the nanoparticle size, administered dose, and age or preexistent pathological state of the study animals [84].

8. Approaches for Increasing the Antibacterial Effect of IONPs

The antimicrobial effect of IONPs can be improved by enhancing their antibacterial activity through external magnetic field application, foreign metal doping, and surface, shape, and size modification, as well as by influencing their biodistribution related to their size, shape, surface charge, and superparamagnetism (Figure 3 and Table 2).
SPIONs possess superparamagnetism, allowing them to undergo magnetization only under a magnetic field. It is notable that SPIONs have the capability to penetrate into bacteria and biofilms and produce localized heat under an external magnetic field. The use of an alternating magnetic field can dramatically improve the antibacterial activity of mesoporous hollow Fe3O4 nanoparticles (MHFPs) against Escherichia coli and Staphylococcus aureus and disperse bacterial biofilms due to the elevated local temperature and vibration damage [85]. Without an external magnetic field, 1000 μg mL−1 MHFPs induced a 22.70% and 23.54% reduction in CFU mL−1 for Escherichia coli and Staphylococcus aureus separately. However, the final counts of CFU mL−1 showed that there were 99.15% and 79.88% reductions in Escherichia coli and Staphylococcus aureus, individually with 1000 μg mL−1 MHFPs after external magnetic field treatment for 25 min.
Doping foreign metals into IONPs exhibited higher antimicrobial activity than IONPs [89,90,91]. Doping is the controlled insertion of a foreign element into the unoccupied crystal lattice to alter the characteristics of nanoparticles [94]. Doped IONPs alter the size and magnetic properties, facilitating interactions with bacteria and increased the charge density of magnetic nanoparticles, promoting ROS production [95]. The size of Fe3O4/ZnO nanoparticles decreased with the Ni dopant concentration, promoting antibacterial activity [90]. The average size of Fe3O4/ZnO was 36 nm, and the size decreased to 33 nm and 28 nm after the doping of 3% and 5% Ni individually. The zone of inhibition value of the Fe3O4/ZnO nanoparticles for both Staphylococcus aureus and Klebsiella pneumoniae was 6 mm individually. Furthermore, the 3% Ni-doped Fe3O4/ZnO nanocomposite increased the zone of inhibition value to 10–11 mm, and higher inhibitory zone values were found to be 11–12 mm for Klebsiella pneumoniae and 13–14 mm for Staphylococcus aureus for 5% Ni. Another study showed that the antibacterial activity of Ag-doped α-Fe2O3 nanoparticles was higher than that of α-Fe2O3 nanoparticles [89]. For Staphylococcus aureus and Bacillus, the zone of inhibition values were about 10 mm for α-Fe2O3 nanoparticles, and the corresponding values were about 14 mm for 5% Ag-doped nanoparticles. The main challenge of using doped IONPs is the choice of doping material. Incorporating hypotoxic metals such as Ag [96] or Au [97] are beneficial to the biocompatibility of doped IONPs.
Surface modification is also an important way to improve the antibacterial properties of IONPs. Hydrophobic negatively charged oleic acid-coated IONPs (OA-IONPs) show stronger antibacterial effects on Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli compared to the unmodified IONPs [69]. Furthermore, 100 μg mL−1 OA-IONPs showed a 61% and 54% reduction in the count of CFU mL−1 for Staphylococcus aureus and Escherichia coli, respectively, whereas the unmodified IONPs had no effect on the growth of these bacteria at the same concentration. Positively charged chitosan-coated IONPs promote interactions with bacteria at the interfaces, resulting in enhancements of ROS production and antimicrobial activity [54]. The viability of Bacillus subtilis and Escherichia coli was reduced by approximately 30% by 50 μM unmodified IONPs, whereas the chitosan-coated IONPs had a significant effect on bacterial viability, and their viability was reduced by approximately 70% in the presence of chitosan-coated IONPs at the same concentration. Coating IONPs with trained immunity agonist β-glucan enhanced the antibacterial action of the IONPs against Escherichia coli, macrophage engulfment of pathogens, and the prevention and treatment of sepsis and secondary infections by inducing trained immunity [92]. Mucilage-coated IONPs, loaded with ciprofloxacin (Fe3O4@QSM-CIP), possess stronger antibacterial activity against standard strains of both Gram-positive and Gram-negative bacteria [93]. Specifically, the zone of inhibition values of Fe3O4 nanoparticles for Bacillus cereus, Escherichia coli, Salmonella typhimurium, and Staphylococcus aureus were 6.4, 7.2, 7.6, and 6.4 mm, whereas the corresponding values of Fe3O4@QSM-CIP extended to 19.9, 24.8, 29.7, 35.8 mm individually. Additionally, size modification and shape modification are alternative approaches to antibacterial activity improvement for IONPs. Applications of relatively small-sized or nonspherical IONPs are preferred due to their stronger antibacterial activity, as mentioned above.
Owing to the biodistribution of IONPs being influenced by their size, shape, surface charge, and superparamagnetism, as previously mentioned, the antibacterial effect of IONPs on some specific tissues and organs can also be improved by governing their biodistribution behavior through modulating the size, shape, and surface charge, besides directing them to the desired site of action using an external magnetic field.

9. Conclusions

Bacterial resistance evolves faster than the creation of new antibacterial agents. The uniqueness of magnetic IONPs brings benefits to their use in antibacterial applications. Among metal oxide nanoparticles, the antibacterial activity of IONPs is relatively weak, whereas IONPs have better biocompatibility [98]. Furthermore, external magnetic fields, foreign metal doping, and surface, size, and shape modification can enhance the antibacterial effect of IONPs. In view of a balance between antimicrobial action and biocompatibility, IONPs are expected to be potential antimicrobial agents of a new generation.

Author Contributions

Conceptualization, T.-G.Z. and C.-Y.M.; writing—original draft preparation, T.-G.Z.; figure design, T.-G.Z.; writing—review and editing, T.-G.Z. and C.-Y.M. All authors have read and agreed to the published version of the manuscript.

Funding

This study was supported by the National Natural Science Foundation of China Young Program, funded by the Chinese government (No. 81903728).

Data Availability Statement

Not applicable.

Acknowledgments

The material used to produce the figures of this article was provided by Servier Medical Art (http://smart.servier.com/), licensed under a Creative Common Attribution 3.0 Generic License (https://creativecommons.org/licenses/by/3.0/, accessed on 1 August 2024).

Conflicts of Interest

The authors declare no conflicts of interest.

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Nanomaterials 14 01311 g001
Figure 1. Antibacterial potential mechanisms of IONPs. (1) Cell wall and cell membrane damage via electrostatic and van der Waals interaction. (2) DNA fragmentation, (3) protein oxidation, and (4) lipid membrane oxidation are caused by ROS.
Figure 1. Antibacterial potential mechanisms of IONPs. (1) Cell wall and cell membrane damage via electrostatic and van der Waals interaction. (2) DNA fragmentation, (3) protein oxidation, and (4) lipid membrane oxidation are caused by ROS.
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Figure 2. Main factors influencing the biodistribution of IONPs. Surface charge, shape, size, and superparamagnetism influencing the biodistribution of IONPs.
Figure 2. Main factors influencing the biodistribution of IONPs. Surface charge, shape, size, and superparamagnetism influencing the biodistribution of IONPs.
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Figure 3. Approaches for increasing the antibacterial effect of IONPs. Surface, shape, size modification, and external magnetic field application improve both the antibacterial activity and biodistribution of IONPs, besides the improvement of antibacterial activity by foreign metal doping. The brown sphere represents bio-substances such as antibiotics or β-glucan.
Figure 3. Approaches for increasing the antibacterial effect of IONPs. Surface, shape, size modification, and external magnetic field application improve both the antibacterial activity and biodistribution of IONPs, besides the improvement of antibacterial activity by foreign metal doping. The brown sphere represents bio-substances such as antibiotics or β-glucan.
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Table 2. Approaches including external magnetic field, foreign metal doping, and surface modification for increasing the antibacterial effect of IONPs.
Table 2. Approaches including external magnetic field, foreign metal doping, and surface modification for increasing the antibacterial effect of IONPs.
MethodNanoparticle TypeBacteriaRef.
External magnetic fieldMesoporous hollow Fe3O4E. coli
S. aureus		[85]
Hydroxyapatite-Fe3O4S. aureus
E. coli		[86]
SPION-encapsulating
polymersome		S. epidermidis biofilms[87]
Fe3O4@Ag@HydroxyapatiteS. aureus biofilms[88]
Foreign metal dopingAg-doped α-Fe2O3S. aureus
Bacillus
Klebsiella
E. col		[89]
Ni-doped Fe3O4/ZnOS. aureus
K. pneumoniae		[90]
Au-doped Fe3O4A. baumannii
S. enterica
S. aureus
M. luteus		[91]
Surface modificationOleic acid-Fe3O4S. aureus
E. coli		[69]
Chitosan-Fe3O4B. subtilis
E. coli		[54]
β-glucan-Fe2O3E. coli.[92]
Fe3O4@QSM-CIPB. cereus
E. coli
S. typhimurium
S. aureus		[93]
QSM: quince seed mucilage; CIP: ciprofloxacin; Ref.: reference.
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Zhang, T.-G.; Miao, C.-Y. Iron Oxide Nanoparticles as Promising Antibacterial Agents of New Generation. Nanomaterials 2024, 14, 1311. https://doi.org/10.3390/nano14151311

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Zhang T-G, Miao C-Y. Iron Oxide Nanoparticles as Promising Antibacterial Agents of New Generation. Nanomaterials. 2024; 14(15):1311. https://doi.org/10.3390/nano14151311

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Zhang, Tian-Guang, and Chao-Yu Miao. 2024. "Iron Oxide Nanoparticles as Promising Antibacterial Agents of New Generation" Nanomaterials 14, no. 15: 1311. https://doi.org/10.3390/nano14151311

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Zhang, T.-G., & Miao, C.-Y. (2024). Iron Oxide Nanoparticles as Promising Antibacterial Agents of New Generation. Nanomaterials, 14(15), 1311. https://doi.org/10.3390/nano14151311

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