Synthesis and biocompatible role of hierarchical structured carbon nanoplates incorporated alpha-Fe2O3 nanocomposites for biomedical applications with respect to cancer treatmentopen access
- Authors
- AlSalhi, Mohamad S.; Devanesan, Sandhanasamy; Shanmugam, Paramasivam; Kim, Young Ock; Kwon, Jun-Tac; Kim, Hak-Jae
- Issue Date
- Feb-2020
- Publisher
- King Saud University
- Keywords
- Biocompatibility; Carbon nanoplates; Cytotoxicity; alpha-Fe2O3; alpha-Fe2O3/C nanocomposites
- Citation
- Saudi Journal of Biological Sciences, v.27, no.2, pp 588 - 593
- Pages
- 6
- Journal Title
- Saudi Journal of Biological Sciences
- Volume
- 27
- Number
- 2
- Start Page
- 588
- End Page
- 593
- URI
- https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/3144
- DOI
- 10.1016/j.sjbs.2019.11.028
- ISSN
- 1319-562X
2213-7106
- Abstract
- This study aimed to inspect the hierarchically structured spherical-like hematite (alpha-Fe2O3) nanoparticles synthesize by simple, low temperature solution combustion process. The uniformly distributed alpha-Fe2O3/carbon nanocomposite (alpha-Fe2O3/C nanocomposite) was prepared by incorporating carbon nanoplates into sphere-like alpha-Fe2O3 nanoparticles. The synthesized nanomaterials were characterized using various techniques such as XRD, FESEM, and EDS. The cytotoxicity of the material was evaluated by MIT assay and nuclear imaging based on the cell morphological changes on both human lung cancerous cell line A549 and chang liver as non cancerous cell line. The results demonstrated that the pure and composite material exhibited above 70% viability on non-cancerous cell line and around 60% inhibition on A549 lung cancer cell line indicates the alpha-Fe2O3/C nanocomposite is biocompatible and can be used for biological applications and anticancer therapy. Cell death induced by alpha-Fe2O3, carbon nanoplates and alpha-Fe2O3 nanocomposites was further evidenced with DAPI. (C) 2019 The Author(s). Published by Elsevier B.V. on behalf of King Saud University.
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Collections - College of Medicine > Department of Clinical Pharmacology > 1. Journal Articles
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