Biocompatible L-Cysteine Capped MoS$_2$ Nanoflowers for Antibacterial Applications: Mechanistic Insights

TL;DR

This study presents a biocompatible, L-cysteine capped MoS2 nanoflower that exhibits strong antibacterial activity against E. coli and S. aureus through oxidative stress mechanisms, with high biocompatibility for potential biomedical applications.

Contribution

It introduces a novel surface modification of MoS2 nanoflowers with L-cysteine, enhancing stability and antibacterial efficacy without external stimuli or drug loading.

Findings

Achieved 97% and 90% bacterial inhibition at 250 μg/mL.

Confirmed antibacterial mechanism involves ROS-dependent and independent oxidative stress.

Demonstrated high biocompatibility with 90% cell viability.

Abstract

The development of multi-drug-resistant bacterial infections seriously threatens public health, so efforts are needed to develop a new class of safe and effective antibacterial agents. Here, we report a bio-inspired synthesis of surface-modified MoS$_2$ Nanoflowers with L-cysteine (MoS$_2$-cys NFs) that show good colloidal stability in an aqueous medium. The FE-SEM and TEM data confirm the flower-like morphology and determine the size of NFs (537+-12 nm); the XRD data predicts the hexagonal crystal structure of the NFs. The XPS peaks confirm the formation of MoS$_2$ NFs with surface modification by L-cysteine. FTIR measurements also confirm the presence of L-cysteine in the NFs. The antibacterial activity of as-prepared MoS$_2$-cys NFs examined over gram-negative Escherichia coli and gram-positive Staphylococcus aureus bacteria shows inhibition of nearly 97% and 90%, respectively, at concentrations 250 $\mu$g/mL each after incubation of 6 hrs. The antibacterial mechanism is mainly attributed to the generation of oxidative stress, which can occur through both ROS-dependent and ROS-independent pathways. The ROS-dependent and ROS-independent oxidative stresses were measured using flow cytometry and fluorescence imaging using DCFH-DA staining, and Ellman's assay, respectively. Moreover, the toxicity studies of the MoS$_2$-cys NFs towards HFF cell lines suggested the high biocompatibility of the nanomaterial with a cell viability of nearly 90%. We report the intrinsic antibacterial efficiency of MoS$_2$-cys NFs without any external stimulus (light, H2O2, etc.), doping, or drug loading. Our study indicates that the proper surface modification can enhance the colloidal stability and antibacterial potency of MoS$_2$-based nanomaterials for further applications such as antibacterial coatings, water disinfection, and wound healing.