The spread of antibiotic resistance and increasing prevalence of biofilm-associated infections is driving demand for new means to treat bacterial infection. Nanotechnology provides an innovative platform for addressing this challenge, with potential to manage even infections involving multidrug-resistant (MDR) bacteria. The current review summarizes recent progress over the last 2 years in the field of antibacterial nanodrugs, and describes their unique properties, mode of action and activity against MDR bacteria and biofilms. Biocompatibility and commercialization are also discussed. As opposed to the more common division of nanoparticles (NPs) into organic- and inorganic-based materials, this review classifies NPs into two functional categories. The first includes NPs exhibiting intrinsic antibacterial properties and the second is devoted to NPs serving as a cargo for delivering antibacterial agents. Antibacterial nanomaterials used to decorate medical devices and implants are reviewed here as well.

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Currently, the technologies accompanying the usage of waste materials for the fabrication of innovative useful materials have been significantly advanced. For the same purpose, a possible sustainable approach was demonstrated for the utilization of jute caddies, known as jute industry waste. From the industrial waste, carbon dots (CDs) were sonochemically prepared, followed by their surface modification with benzalkonium chloride (BZC) to yield waste jute-derived fluorescent surface-quaternized CDs (JB-CDs), which exhibit excellent water solubility, excitation-dependent emission, and good photostability, and were utilized as a fluorescent nanoswitch to detect inorganic pollutants, such as chromium (VI) [Cr­(VI)] ions, in aqueous solutions. JB-CDs can detect Cr­(VI) concentrations as low as 0.03 μM through luminescence quenching (“turn-off”) and further recover their fluorescence (“turn-on”) selectively for sensing ascorbic acid (AA), compared with other metal ions and biomolecules tested. The present technique has the advantages of fast response time and high selectivity and sensitivity in practical applications. JB-CDs were tested against a Gram-negative bacterium, Escherichia coli, and a Gram-positive bacterium, Staphylococcus aureus, to confirm their bactericidal activity. The results indicated that JB-CDs substantially inhibited the growth of the tested bacteria. Besides this, JB-CDs played the role of a nanovehicle to exemplify the release study of a model drug ciprofloxacin. It was observed that the surface-quaternized JB-CDs showed a pH-responsive release behavior, where the release behavior was found to be better controlled at pH 7.4 than at pH 5.2 and 6.8. The synthesis of such a fluorescent nanobutton, stimuli-responsive drug release, and antibacterial nanomaterial using a sustainable material such as jute industrial waste can pave the path for a smart multifunctional material.

Increased resistance of bacteria to disinfection and antimicrobial treatment poses a serious public health threat worldwide. This has prompted the search for agents that can inhibit both bacterial growth and withstand harsh conditions (e.g., high organic loads). In the current study, N-halamine-derivatized cross-linked polymethacrylamide nanoparticles (NPs) were synthesized by copolymerization of the monomer methacrylamide (MAA) and the cross-linker monomer N,N-methylenebis(acrylamide) (MBAA) and were subsequently loaded with oxidative chlorine using sodium hypochlorite (NaOCl). The chlorinated NPs demonstrated remarkable stability and durability to organic reagents and to repetitive bacterial loading cycles as compared with the common disinfectant NaOCl (bleach), which was extremely labile under these conditions. The antibacterial mechanism of the cross-linked P(MAA-MBAA)-Cl NPs was found to involve generation of reactive oxygen species (ROS) only upon exposure to organic media. Importantly, ROS were not generated upon suspension in water, revealing that the mode of action is target-specific. Further, a unique and specific interaction of the chlorinated NPs with Staphylococcus aureus was discovered, whereby these microorganisms were all specifically targeted and marked for destruction. This bacterial encircling was achieved without using a targeting module (e.g., an antibody or a ligand) and represents a highly beneficial, natural property of the P(MAA-MBAA)-Cl nanostructures. Our findings provide insights into the mechanism of action of P(MAA-MBAA)-Cl NPs and demonstrate the superior efficacy of the NPs over bleach (i.e., stability, specificity, and targeting). This work underscores the potential of developing sustainable P(MAA-MBAA)-Cl NP-based devices for inhibiting bacterial colonization and growth.

The emergence of antibiotic resistance of pathogenic bacteria has led to renewed interest in exploring the potential of plant-derived antimicrobials e.g., essential oils (EOs), as an alternative strategy to reduce microbial contamination. However, the volatile nature of EOs presents a major challenge in their incorporation into polymers by conventional high-temperature processing techniques. Herein, we employ halloysite nanotubes (HNTs) as efficient nano-carriers for carvacrol (a model EO). This precompounding encapsulation step imparts enhanced thermal stability to the carvacrol, allowing for its subsequent melt compounding with low-density polyethylene (LDPE). The resulting polymer nanocomposites exhibit outstanding antimicrobial properties with a broad spectrum of inhibitory activity against Escherichia coli, Listeria innocua in biofilms, and Alternaria alternata. Their antimicrobial effectiveness is also successfully demonstrated in complex model food systems (soft cheese and bread).This superior activity, compared to other studied carvacrol containing films, is induced by the significantly higher carvacrol content in the film as well as its slower out-diffusion from the hybrid system. Thus, these new active polymer nanocomposites presents an immense potential in controlling microbial contamination and biofilm related adverse effects, rendering them as excellent candidate materials for a wide range of applications.

A simple one-step process for the polymerization of dopamine has been developed using nitrogen-doped carbon dots (N@C–dots) as the sole initiator. The synthesized amorphous polydopamine (PDA)-doped N@C–dots (PDA–N@C–dots composite) exhibited a negative charge of –39 mV with particle sizes ranging from 200 to 1700 nm. The stable colloidal solution was active against methicillin-resistant Staphylococcus aureus (MRSA), a Gram-negative bacterium. The strong adhesion of the polymer to the bacterial membrane resulted in a limited diffusion of nutrients and wastes in and out of the cell cytosol, which is a generic mechanism to trigger cell death. Another possible route is the autoxidation of the catechol moiety of PDA to form quinone and release reactive oxygen species (ROS) such as superoxide radicle and hydrogen peroxide, two well-known ROS with antimicrobial properties against both Gram-negative and Gram-positive bacteria.

In recent years, lignin has drawn increasing attention for different applications due to its intrinsic antibacterial and antioxidant properties, coupled with biodegradability and biocompatibility. However, chemical modification or combination with metals is usually required to increase its antimicrobial functionality and produce biobased added-value materials for applications wherein bacterial growth should be avoided, such as biomedical and food industries. In this work, a sonoenzymatic approach for the simultaneous functionalization and nanotransformation of lignin to prepare metal-free antibacterial phenolated lignin nanoparticles (PheLigNPs) is developed. The grafting of tannic acid, a natural phenolic compound, onto lignin was achieved by an environmentally friendly approach using laccase oxidation upon the application of high-intensity ultrasound to rearrange lignin into NPs. PheLigNPs presented higher antibacterial activity than nonfunctionalized LigNPs and phenolated lignin in the bulk form, indicating the contribution of both the phenolic content and the nanosize to the antibacterial activity. Studies on the antibacterial mode of action showed that bacteria in contact with the functionalized NPs presented decreased metabolic activity and high levels of reactive oxygen species (ROS). Moreover, PheLigNPs demonstrated affinity to the bacterial surface and the ability to cause membrane destabilization. Antimicrobial resistance studies showed that the NPs did not induce resistance in pathogenic bacteria, unlike traditional antibiotics.

Essential oils (EOs) have a long history as food preservatives and many advantages compared to synthetic preservatives. The major limitation of EOs as antimicrobial agents incorporated into a polymeric matrix is their low thermal stability and their high volatility from polymers. This study suggests a new methodology approach to bypass the key limitations of adding EOs into active packaging, as food preservatives. Antimicrobial active films based on linear low density polyethylene (LLDPE) and Montmorillonite (MMT) were produced by incorporating the EO thymol in a stepwise procedure. The production of the film composites, containing thymol, has been conducted, under a protocol of three stages: (1) production of a highly porous nano composite master batch; (2) impregnation of thymol into the master batch; and (3) cast film extrusion. Adding MMT incorporated together with a foaming agent at stage‐(1) increased significantly the heat stability of the EO during melt processing at stage‐(3). Finally, the film obtained showed a high antimicrobial activity. The results obtained have proven the synergistic interaction between MMT, foaming agent and thymol. As the MMT content in the film increased, the loss of EO in the processing decreased, leading to a natural antimicrobial film with improved antibacterial properties. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 40564.