Synthesis and biocompatible role of hierarchical structured carbon nanoplates incorporated α-Fe2O3 nanocomposites for biomedical applications with respect to cancer treatment

被引:17
作者
AlSalhi, Mohamad S. [1 ]
Devanesan, Sandhanasamy [1 ]
Shanmugam, Paramasivam [2 ]
Kim, Young Ock [3 ]
Kwon, Jun-Tac [4 ]
Kim, Hak-Jae [4 ]
机构
[1] King Saud Univ, Coll Sci, Dept Phys & Astron, POB 2455, Riyadh 11451, Saudi Arabia
[2] St Joseph Univ, Dept Chem, Dimapur 797115, Nagaland, India
[3] Chungnam Natl Univ, Coll Agr & Life Sci, Dept Bioenvironm Chem, 99 Daehak Ro, Daejeon 34134, South Korea
[4] Soonchunhyang Univ, Coll Med, Dept Clin Pharmacol, Cheonan, South Korea
关键词
Biocompatibility; Carbon nanoplates; Cytotoxicity; alpha-Fe2O3; alpha-Fe2O3/C nanocomposites; HEMATITE NANOPARTICLES; MAGNETIC-PROPERTIES; CYTOTOXICITY; ELECTRODE; TOXICITY;
D O I
10.1016/j.sjbs.2019.11.028
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:588 / 593
页数:6
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