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Biosynthesis of reduced graphene oxide using Turbinaria ornata and its cytotoxic effect on MCF‐7 cells
Graphene‐based nanomaterials are gaining importance in biomedicine because of their large surface areas, solubility, and biocompatibility. Green synthesis is the most economical method for application, as it is rapid and sustainable. Biofunctionalized reduced graphene oxide (TrGO) nanosheets were sy...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675839/ https://www.ncbi.nlm.nih.gov/pubmed/34694710 http://dx.doi.org/10.1049/nbt2.12057 |
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author | Smita, K. M. Abraham, L. Stanley Kumar, V. Ganesh Vasantharaja, Raguraman Thirugnanasambandam, R. Antony, Ajit Govindaraju, K. Velan, T. Senthil |
author_facet | Smita, K. M. Abraham, L. Stanley Kumar, V. Ganesh Vasantharaja, Raguraman Thirugnanasambandam, R. Antony, Ajit Govindaraju, K. Velan, T. Senthil |
author_sort | Smita, K. M. |
collection | PubMed |
description | Graphene‐based nanomaterials are gaining importance in biomedicine because of their large surface areas, solubility, and biocompatibility. Green synthesis is the most economical method for application, as it is rapid and sustainable. Biofunctionalized reduced graphene oxide (TrGO) nanosheets were synthesized using methanol extract of Turbinaria ornata, and bioreduction of graphene oxide was primarily confirmed and characterized using UV‐visible, Fourier transform infrared (FTIR), and X‐ray diffraction spectroscopy and further characterized by zeta potential and transmission electron microscopy. The FTIR spectra of TrGO showed a decrease in the band intensities of oxygen groups, thus confirming effective deoxygenation. The zeta potential value of −34.6 mV revealed that synthesized TrGO was highly stable. The cytotoxic effect of TrGO against MCF‐10A and MCF‐7 cells was ascertained using MTT assay, showed a greater cytotoxic effect on MCF‐7 cells. The IC(50) of TrGO treatment against MCF‐7 was calculated to be 31.25 µg, which is onefold lower than the cytotoxic effect of methanolic extract of T. ornata (60.0 ± 1.14 µg/ml). In addition, there was a statistically significant difference in cell viability between MCF‐10A and MCF‐7 cells in the treatment of TrGO. Hence, this study results in an efficient green reductant for producing rGO nanosheets that possess cytotoxicity against breast cancer cells. |
format | Online Article Text |
id | pubmed-8675839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86758392022-02-03 Biosynthesis of reduced graphene oxide using Turbinaria ornata and its cytotoxic effect on MCF‐7 cells Smita, K. M. Abraham, L. Stanley Kumar, V. Ganesh Vasantharaja, Raguraman Thirugnanasambandam, R. Antony, Ajit Govindaraju, K. Velan, T. Senthil IET Nanobiotechnol Original Research Paper Graphene‐based nanomaterials are gaining importance in biomedicine because of their large surface areas, solubility, and biocompatibility. Green synthesis is the most economical method for application, as it is rapid and sustainable. Biofunctionalized reduced graphene oxide (TrGO) nanosheets were synthesized using methanol extract of Turbinaria ornata, and bioreduction of graphene oxide was primarily confirmed and characterized using UV‐visible, Fourier transform infrared (FTIR), and X‐ray diffraction spectroscopy and further characterized by zeta potential and transmission electron microscopy. The FTIR spectra of TrGO showed a decrease in the band intensities of oxygen groups, thus confirming effective deoxygenation. The zeta potential value of −34.6 mV revealed that synthesized TrGO was highly stable. The cytotoxic effect of TrGO against MCF‐10A and MCF‐7 cells was ascertained using MTT assay, showed a greater cytotoxic effect on MCF‐7 cells. The IC(50) of TrGO treatment against MCF‐7 was calculated to be 31.25 µg, which is onefold lower than the cytotoxic effect of methanolic extract of T. ornata (60.0 ± 1.14 µg/ml). In addition, there was a statistically significant difference in cell viability between MCF‐10A and MCF‐7 cells in the treatment of TrGO. Hence, this study results in an efficient green reductant for producing rGO nanosheets that possess cytotoxicity against breast cancer cells. John Wiley and Sons Inc. 2021-05-18 /pmc/articles/PMC8675839/ /pubmed/34694710 http://dx.doi.org/10.1049/nbt2.12057 Text en © 2021 The Authors. IET Nanobiotechnology published by John Wiley & Sons Ltd on behalf of The Institution of Engineering and Technology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Paper Smita, K. M. Abraham, L. Stanley Kumar, V. Ganesh Vasantharaja, Raguraman Thirugnanasambandam, R. Antony, Ajit Govindaraju, K. Velan, T. Senthil Biosynthesis of reduced graphene oxide using Turbinaria ornata and its cytotoxic effect on MCF‐7 cells |
title | Biosynthesis of reduced graphene oxide using Turbinaria ornata and its cytotoxic effect on MCF‐7 cells |
title_full | Biosynthesis of reduced graphene oxide using Turbinaria ornata and its cytotoxic effect on MCF‐7 cells |
title_fullStr | Biosynthesis of reduced graphene oxide using Turbinaria ornata and its cytotoxic effect on MCF‐7 cells |
title_full_unstemmed | Biosynthesis of reduced graphene oxide using Turbinaria ornata and its cytotoxic effect on MCF‐7 cells |
title_short | Biosynthesis of reduced graphene oxide using Turbinaria ornata and its cytotoxic effect on MCF‐7 cells |
title_sort | biosynthesis of reduced graphene oxide using turbinaria ornata and its cytotoxic effect on mcf‐7 cells |
topic | Original Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675839/ https://www.ncbi.nlm.nih.gov/pubmed/34694710 http://dx.doi.org/10.1049/nbt2.12057 |
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