Abstract
Hexagonal molybdenum trioxide (h-MoO3) was synthesized using egg white with MoO3 precursor, which was further treated with nitric acid (HNO3) by solution-based chemical precipitation technique for comparison without treatment. The XRD analysis confirms the formation of metastable phase with hexagonal crystal system for h-MoO3 with and without HNO3 treatment. Subsequently, the result indicate that the HNO3 treated h-MoO3 shows enhanced crystalline behavior compared to untreated h-MoO3. Raman and FTIR analysis confirmed the formation of h-MoO3 where the variation in intensity of the peaks were observed when comparing h-MoO3 with and without HNO3 treatment as well as due to the changes in the crystalline structure of the samples. The band gaps obtained from Tauc plot for the synthesized h-MoO3 with and without HNO3 treatment were 3.17 eV and 3.26 eV, respectively. Observations by HRSEM and HRTEM allowed confirming the formation of nanorod and nanoplate like structures for h-MoO3 treated with and without HNO3, respectively. In addition, the increased crystallinity of the HNO3 treated h-MoO3 was displayed higher anti-bacterial activity than untreated h-MoO3 with zones of inhibition values of 14 ± 1 and 12 ± 1 mm against multi drug resistant (MDR) E. coli and K. pneumoniae, respectively. Subsequently, the quantitative analysis of HNO3 treated h-MoO3 demonstrated 94% and 96% inhibition against E. coli and K. pneumoniae, respectively, at 250 µg/mL concentration. Oxidative stress mediated membrane damages and surface morphology alterations were observed after exposure of HNO3-treated h-MoO3 (improved crystallinity) against E. coli and K. pneumoniae as suggested by confocal laser scanning electron microscopy and scanning electron microscopy. Furthermore, very minimal cytotoxicity to human alveolar epithelial cell line (A549) for HNO3 treated h-MoO3 was observed, suggesting that this material is benign. The present study indicates that the enhanced crystallinity of HNO3 treated h-MoO3 synthesized in the presence of egg white can be considered as a promising alternative drug target material to fight against MDR bacteria.
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Data sets generated during the current study are available from the corresponding author on reasonable request.
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Acknowledgements
MD would like to thank and acknowledge SCIF, SRMIST, Kattankulathur for providing the instrumentation facilities and SRMIST, Ramapuram campus for research support. The authors express their sincere appreciation to the Researchers Supporting Project Number (RSP2024R70), King Saud University, Riyadh, Saudi Arabia.
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This work was supported by Researchers Supporting Project Number (RSP2024R70), King Saud University, Riyadh, Saudi Arabia.
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M. Dhanasekar designed the entire work, conceptualization, synthesis of nanomaterial, data curation, writing original draft and supervision of the manuscript. Mudaliar Mahesh Margoni contributed in synthesis and characterization of nanomaterial formal analysis and writing part of the manuscript. Gnansekaran Chackaravarthi and Govindan Rajivgandhi contributed in the biological experiment, writing, and interpretation part of the manuscript. Muthuchamy Maruthupandy contributed entire cytotoxicity part of the manuscript. Nandhu Suresh contributed on the collection of resources, arrangement and material synthesis. V. Krishna involved in the interpretation and writing part of the nanomaterial. Ali Akbari-Fakhrabadi participated in the review& editing process. Franck Quero contributed in biological part of the entire manuscript. Natesan Manoharan contributed in the design, concept and analysis of the biological part of the manuscript. N. Asokan and Sakthivel Sankaran contributed in the review, writing and graphical representation of the manuscript. Naiyf. S. Alharbi contributed in the toxicity analysis of the manuscript.
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Dhanasekar, M., Margoni, M.M., Rajivgandhi, G. et al. Enhanced Crystallinity Behavior of Egg White Mediated h-MoO3 Using Acid Precipitation Method for Improved Anti-Bacterial Properties against Multi Drug Resistant Bacteria. J Clust Sci (2024). https://doi.org/10.1007/s10876-024-02626-9
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DOI: https://doi.org/10.1007/s10876-024-02626-9