No abstract

In the present study, we report the formulation, characterization, and in vitro antibacterial and cytotoxicity effects of exopolysaccharide (EPS) stabilized iron oxide nanoparticles (FeONPs) against the human epidermoid carcinoma cell line (A431). EPS is extracted from a spore-forming strain of Bacillus subtilis, VT03, isolated from the gut microbiome of the freshwater fish Oreochromis mossambicus (Tilapia). FTIR, 1 H NMR and 13 C NMR spectroscopic studies show the presence of sugar moieties, confirming that EPS might be a glucan. Later, EPS is used as an eco-friendly reducing and stabilizing agent for the formulation of iron oxide nanoparticles (FeONPs). Initially, the generation of nanoscale FeO was confirmed through the formation of a black-coloured precipitate with an absorbance maxima at 250-300 nm in a UV-visible spectrometer. X-ray diffraction (XRD) planes clearly confirm that the synthesized FeONPs are in the cubic spinel phase. The morphometric features of the synthesized FeONPs are exclusively studied using electron microscopy (FESEM and HRTEM) which shows spherical FeONPs in sizes ranging between 75-120 nm; the mean size was found to be 106 AE 12 nm. Additionally, energy dispersive X-ray analysis (EDAX), selected area emission diffraction (SAED) and dynamic light scattering (DLS) confirms the purity and homogeneity of the synthesized FeONPs. The vibrating sample magnetometer (VSM) technique reveals the presence of both ferro-and antiferromagnetic phases in the EPS-stabilized FeONPs. Further, the inhibitory activity of EPS-stabilized FeONPs against human and fish pathogenic strains such as Aeromonas hydrophila (ATCC 49140), Aeromonas hydrophila (MTCC 1739), Aeromonas sobria (MTCC 3613) and Aeromonas hydrophila (obtained from OIE Reference Laboratory, C. Abdul Hakeem College, Melvisharam) was assessed. The in vitro cytotoxicity effects of free EPS and EPSstabilized FeONPs were probed in the human epidermoid carcinoma cell line A431. The IC 50 values of EPS and EPS-stabilized FeONPs were found to be 350.18 and 62.946 mg ml À1 respectively. Further, acridine orange/ethidium bromide (AO/EtBr) staining of A431 cells at different time intervals clearly distinguishes the live cells and the cells that have undergone apoptotic cell death. In conclusion, our research paves the way for a facile and greener route to synthesize FeONPs at room temperature. On the other hand, this study also proves that the formulated multifunctional hybrid FeONPs have remarkable qualities such as enhanced bioavailability and magnetic properties. This can be developed into a successful theragnostic platform for cancer treatment.D-galactose, L-rhamnose, and N-acetylglucosamine (GlcNAc), N-acetylgalactosamine (GalNAc) or glucuronic acid (GlcA)) based on the linkage bonds and nature of the monomeric units. Non-carbohydrate content may be present in a few cases, such as phosphate, acetyl and glycerol. 3 1,4-b-or 1,3-b-linkages and

No abstract

No abstract

The objective of the present work was to isolate and characterize the exopolymer producer from a marine environment. The exopolymer producing strain (S13) was identified as Bacillus thuringiensis S13. Characterization of exopolymer shows the presence of brominated compound responsible for cytotoxicity on lung cancer cell line (A549) on XTT assay. An in vitro study of bacterial exopolymer shows the presence of cytotoxic effects on cell lines. Further, active compound in exopolymer responsible for cytotoxicity has to be characterized. The exopolymer produced by B. thuringiensis S13, showed potent cytotoxic effects, and could be used as therapy in cancer after further studies.