Fe-Doped MoS2 Nanozyme for Antibacterial Activity and Detoxification of Mustard Gas Simulant.

The peroxidase-like catalytic activity of various nanozymes was extensively applied in various fields. In this study, we have demonstrated the preparation of Fe-doped MoS2 (Fe@MoS2) nanomaterials with enhanced peroxidase-like activity of MoS2 in a co-catalytic pathway. In view of Fenton reaction, the peroxidase-like Fe@MoS2 nanozyme prompted the decomposition of hydrogen peroxide (H2O2) to a reactive hydroxyl radical (·OH). The efficient decomposition of H2O2 in the presence of Fe@MoS2 has been employed toward the antibacterial activity and detoxification of mustard gas simulant. The combined effect of Fe@MoS2 and H2O2 showed remarkable antibacterial activity against the drug-resistant bacterial strain methicillin-resistant Staphylococcus aureus and Escherichia coli with the use of minimal concentration of H2O2. Fe@MoS2 was further applied for the detoxification of the chemical warfare agent sulfur mustard simulant, 2-chloroethyl ethyl sulfide, by selective conversion to the nontoxic sulfoxide. This work demonstrates the development of a hybrid nanozyme and its environmental remediation from harmful chemicals to microbes.

Superparamagnetic Nickel Nanocluster-Embedded MoS2 Nanosheets for Gram-Selective Bacterial Adhesion and Antibacterial Activity.

Ever increasing infectious diseases caused by pathogenic bacteria are creating one of the greatest health problems. The extensive use of numerous antibiotics and antimicrobial agents has prompted the growth of multidrug-resistant bacterial strains. The ancient biomedical application of metals and the recent advancement in the field of nanotechnology have encouraged us to explore the antimicrobial activity of nanomaterials. Herein, we have synthesized a magnetically separable superparamagnetic nickel nanocluster-loaded two-dimensional molybdenum disulfide nanocomposite (Ni@2D-MoS2). It can selectively bind with Gram-positive bacteria such as methicillin-resistant Staphylococcus aureus (MRSA) and Enterococcus faecalis over Gram-negative bacteria such as Escherichia coli and Pseudomonas aeruginosa. After the functionalization of Ni@2D-MoS2 with a positively charged ligand, it showed an excellent Gram-selective antibacterial activity toward MRSA and E. faecalis. Furthermore, the superparamagnetic property of the synthesized material can be used for the simultaneous removal and killing of the microbes and recycled for further use. This study demonstrates strategies to develop hybrid antimicrobial nanomaterial systems for selective antibacterial activity with recyclability.

Self-Assembled Pd12 Coordination Cage as Photoregulated Oxidase-Like Nanozyme.

Designing supramolecular architectures with uncommon geometries embedded with functional building units is of immense importance in contemporary research. In this report, we present a new water-soluble Pd12L6 supramolecular coordination nanocage (1) that was synthesized via self-assembly of a tetradentate donor (L) with ditopic acceptor cis-[(en)Pd(NO3)2] [en = ethylenediamine]. Self-assembly of a tetratopic donor with a cis-blocked 90° acceptor commonly produces tri/tetra- or hexagonal barrel-type structures. However, the resulting cage 1 has an uncommon geometry consisting of two triangular cupolas conjoined through an irregular common hexagonal base. Incorporation of the benzothiadiazole unit in the structure helped in the photogeneration of reactive oxygen species (ROS) in water. Many nanomaterials have shown to have the ability to mimic the catalytic activity of natural enzymes (nanozymes). Majority of such nanozymes are water insoluble metal/metal-oxide nanoparticles or extended metal organic frameworks (MOFs)/metal-carbon composites, etc. The present water-soluble Pd12 nanocage 1 has shown excellent oxidase-like activity upon irradiation with white light. The enzymatic activity of 1 is photoregulated which offers other obvious advantages, such as external control of enzymatic activity and noninvasiveness. The oxidase-like activity and exogenous ROS generation have been further exploited in photocatalytic antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) bacterial strain.

2D-MoS2-Based ß-Lactamase Inhibitor for Combination Therapy against Drug-Resistant Bacteria.

Despite the remarkable improvement in modern medicine, the ever-increasing abundance of antibiotic-resistant microorganisms remains a catastrophic threat to global health care. ß-Lactamase is playing one of the major roles in antibiotic resistance by making the conventional antibacterial agents abortive by destroying their lactam ring. The combination therapy of traditional antibiotics along with ß-lactamase inhibitors is a potential solution to this problem. In this work, we have screened various functionalized two-dimensional molybdenum disulfide (2D-MoS2) nanomaterials as enzyme inhibitors that effectively bind with ß-lactamase enzyme and reveal competitive inhibition. Among these, carboxylate-functionalized negatively charged 2D-MoS2 is the most potent inhibitor, and in vitro combinatorial application of this with conventional antibiotics has been able to remarkably suppress relevant drug-resistant bacterial growth rate. This study will help to further explore different surface-functionalized 2D nanomaterials with improved ß-lactamase inhibition to fight against multidrug-resistant bacterial infections.