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Graphene Oxide-Gallic Acid Nanodelivery System for Cancer Therapy
Dena Dorniani1,2, Bullo Saifullah2, Farahnaz Barahuie2,3
1Department of Chemistry, University of Sheffield, Dainton Building, Brook Hill, Sheffield, S3 7HF, UK.
Abstract:
Despite the technological advancement in the biomedical science, cancer remains a life-threatening disease. In this study, we designed an anticancer nanodelivery system using graphene oxide (GO) as nanocarrier for an active anticancer agent gallic acid (GA). The successful formation nanocomposite (GOGA) was characterized using XRD, FTIR, HRTEM, Raman, and UV/Vis spectroscopy. The release study shows that the release of GA from the designed anticancer nanocomposite (GOGA) occurs in a sustained manner in phosphate-buffered saline (PBS) solution at pH 7.4. In in vitro biological studies, normal fibroblast (3T3) and liver cancer cells (HepG2) were treated with different concentrations of GO, GOGA, and GA for 72 h. The GOGA nanocomposite showed the inhibitory effect to cancer cell growth without affecting normal cell growth. The results of this research are highly encouraging to go further for in vivo studies.
Insights
This study developed a graphene oxide (GO) and gallic acid (GA) nanocomposite (GOGA) for targeted cancer therapy. The GOGA system effectively inhibited liver cancer cell growth while sparing normal cells.
Area of Science:
- Biomedical Science
- Nanotechnology
- Materials Science
Background:
- Cancer remains a significant global health challenge despite advances in biomedical science.
- Developing effective and targeted drug delivery systems is crucial for improving cancer treatment outcomes.
- Graphene oxide (GO) offers potential as a nanocarrier due to its unique properties.
Purpose of the Study:
- To design and characterize a novel anticancer nanodelivery system using graphene oxide (GO) as a carrier for gallic acid (GA).
- To evaluate the in vitro efficacy of the developed gallic acid-graphene oxide nanocomposite (GOGA) against liver cancer cells.
Main Methods:
- Synthesis and characterization of the gallic acid-graphene oxide nanocomposite (GOGA) using techniques like XRD, FTIR, HRTEM, Raman, and UV/Vis spectroscopy.
- In vitro release studies of gallic acid from the GOGA nanocomposite in phosphate-buffered saline (PBS) at pH 7.4.
- In vitro cytotoxicity assays using normal fibroblast (3T3) and liver cancer cells (HepG2) treated with GO, GOGA, and GA.
Main Results:
- The GOGA nanocomposite was successfully synthesized and characterized.
- Sustained release of gallic acid from the GOGA nanocomposite was observed at physiological pH (7.4).
- The GOGA nanocomposite demonstrated significant inhibition of liver cancer cell (HepG2) growth without adversely affecting normal fibroblast cells (3T3).
Conclusions:
- The developed GOGA nanocomposite is a promising targeted anticancer nanodelivery system.
- This system exhibits selective toxicity towards cancer cells, highlighting its therapeutic potential.
- Further in vivo studies are warranted to explore the full therapeutic capabilities of the GOGA nanocomposite.
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