In the present study, biocompatible manganese nanoparticles have been linked with zinc and iron molecules to prepare different derivatives of MnZnErYFeO NPs (x = 0.02, 0.04, 0.06, 0.08, 0.10), using an ultrasonication approach. The structure, surface morphology, and chemical compositions of MnZnErYFeO NPs were elucidated by X-ray diffractometer (XRD), High-resolution transmission electron microscopy (HR-TEM), scanning electron microscope (SEM), and Energy Dispersive X-Ray Analysis (EDX) techniques. The bioactivity of MnZnErYFeO NPs on normal (HEK-293) and (HCT-116) colon cancer cell line was evaluated. The MnZnErYFeO NPs treatment post 48 h resulted in a significant reduction in cells (via MTT assay, having an IC value between 0.88 µg/mL and 2.40 µg/mL). The specificity of MnZnErYFeO NPs were studied by treating them on normal cells line (HEK-293). The results showed that MnZnErYFeO NPs did not incur any effect on HEK-293, which suggests that MnZnErYFeO NPs selectively targeted the colon cancerous cells. Using , antifungal activity was also studied by evaluating minimum inhibitory/fungicidal concentration (MIC/MFC) and the effect of nanomaterial on the germ tube formation, which exhibited that NPs significantly inhibited the growth and germ tube formation. The obtained results hold the potential to design nanoparticles that lead to efficient bioactivity.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150661PMC
http://dx.doi.org/10.3390/biom11050703DOI Listing

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