Please use this identifier to cite or link to this item:
https://hdl.handle.net/10356/164383
Title: | Ball-milled graphene quantum dots for enhanced anti-cancer drug delivery | Authors: | Prabhakar, Arun Kumar Ajith, M.P. Ananthanarayanan, Arundithi Routh, Parimal Mohan, Babu Cadiam Thamizhchelvan, Anbu Mozhi |
Keywords: | Engineering::Bioengineering | Issue Date: | 2022 | Source: | Prabhakar, A. K., Ajith, M., Ananthanarayanan, A., Routh, P., Mohan, B. C. & Thamizhchelvan, A. M. (2022). Ball-milled graphene quantum dots for enhanced anti-cancer drug delivery. OpenNano, 8, 100072-. https://dx.doi.org/10.1016/j.onano.2022.100072 | Project: | MOE2011-T2–2–010 | Journal: | OpenNano | Abstract: | Graphene quantum dots (GQDs) exhibit excellent opto-electronic properties along with fine-tunable structure and surface properties, which have made them versatile drug carriers. Here GQDs were prepared using carbon black as precursor through oxidation and ball-milling. The prepared GQDs were found to be nano-sized, oxidized, water-soluble and highly fluorescent. The GQDs were found to be extremely biocompatible against the tested cell lines namely: LO2, HeLa, PC-12 and MCF-7 and uptaken by cancer cells in greater amounts with increased concentrations and incubation times. B-Lapachone, an anti-cancer hydrophobic drug, was loaded onto the GQDs through pi-pi bonding and tested for its release profile through dialysis. The drug was released at a significantly higher rate at acidic pH specifically, to cancer cells as compared to the normal cell's relative alkaline pH. The GQD-drug conjugate was found to exhibit enhanced cytotoxicity in cancer cell lines relative to free drug from MTT assay. In whole, sized-down GQDs, having excellent biocompatibility and photostability with enhanced drug delivery properties has been designed and tested. | URI: | https://hdl.handle.net/10356/164383 | ISSN: | 2352-9520 | DOI: | 10.1016/j.onano.2022.100072 | Rights: | © 2022 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
Appears in Collections: | SCBE Journal Articles |
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1-s2.0-S2352952022000342-main.pdf | 7.28 MB | Adobe PDF | View/Open |
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