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Efficient Green Synthesis of (Fe(3)O(4)) and (NiFe(2)O(4)) Nanoparticles Using Star Anise (Illicium verum) Extract and Their Biomedical Activity against Some Cancer Cells

Magnetite Fe(3)O(4) and spinel (2:1) and (4:1) NiFe(2)O(4) magnetic nanoparticles (MNPs) were prepared by simple and affordable co-precipitation methods using an extract of star anise (Illicium verum) as a green reducing agent. The morphology and chemical composition of these MNPs were confirmed by...

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Detalles Bibliográficos
Autores principales: Al-Qasmi, Noha, Almughem, Fahad A., Jarallah, Somayah J., Almaabadi, Amani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324409/
https://www.ncbi.nlm.nih.gov/pubmed/35888298
http://dx.doi.org/10.3390/ma15144832
Descripción
Sumario:Magnetite Fe(3)O(4) and spinel (2:1) and (4:1) NiFe(2)O(4) magnetic nanoparticles (MNPs) were prepared by simple and affordable co-precipitation methods using an extract of star anise (Illicium verum) as a green reducing agent. The morphology and chemical composition of these MNPs were confirmed by field-emission scanning electron microscopy, energy-dispersive X-ray spectroscopy, UV–visible spectroscopy, and X-ray diffraction (XRD). The synthesized magnetite Fe(3)O(4) and spinel (2:1) and (4:1) NiFe(2)O(4) MNPs were in the size range of 0.1–1 µm. The MNPs had irregular clustered platelets (magnetite Fe(3)O(4)) and pyramidal structures (spinel (2:1) and (4:1) NiFe(2)O(4) NPs). The average sizes of the synthesized magnetite Fe(3)O(4), and spinel (2:1) and (4:1) NiFe(2)O(4) MNPs calculated using XRD analysis were 66.8, 72.5, and 72.9 nm, respectively. In addition to the characteristic absorption peaks of magnetite Fe(3)O(4), those of spinel (2:1) and (4:1) NiFe(2)O(4) MNPs were detected at ~300–350 nm and ~700 nm, respectively. Overall, the results of this study indicate that the synthesized magnetite Fe(3)O(4), and spinel (2:1) and (4:1) NiFe(2)O(4) MNPs showed high biomedical activities against liver carcinoma cells and non-small lung adenocarcinoma cells.