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Noncovalent Functionalized Graphene Nanocarriers from Graphite for Treating Thyroid Cancer Cells
Suguna Perumal1, Prakash Gangadaran2,3, Ye Won Bae1
1Department of Applied Chemistry, School of Engineering, Kyungpook National University, Buk-gu, Daehak-ro 80, Daegu 41566, Republic of Korea.
ACS Biomaterials Science & Engineering
|April 19, 2021
Summary
New biocompatible graphene nanocarriers loaded with iron oxide nanoparticles show promise for targeted thyroid cancer therapy. These nanocarriers effectively deliver doxorubicin, inducing cancer cell death via apoptosis and DNA damage.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Cancer Therapy
Background:
- Development of novel nanocarriers for targeted drug delivery is crucial for improving cancer treatment efficacy.
- Graphene and iron oxide nanoparticles offer unique properties for biomedical applications.
- Existing methods for preparing graphene-based nanocarriers often involve multiple steps and harsh conditions.
Purpose of the Study:
- To synthesize biocompatible graphene nanocarriers decorated with iron oxide nanoparticles (IONPs) using a direct graphite approach.
- To evaluate the potential of these nanocarriers for targeted drug delivery in thyroid cancer.
- To investigate the cytotoxicity and cellular mechanisms of action of drug-loaded nanocarriers.
Main Methods:
- One-pot synthesis of graphene nanocarriers (in situ GIOPMPC) via copolymerization of 2-(methacryloyloxy)ethyl phosphorylcholine (MPC) and poly(ethylene glycol) monomethacrylate (PEGMA) in the presence of IONPs and graphite.
- Characterization of nanocarriers using various analytical techniques to confirm composition and distribution.
- In vitro cytotoxicity assays on bioluminescently reported thyroid cancer cells using doxorubicin (DOX)-loaded nanocarriers.
- Signaling pathway analysis to elucidate the mechanism of cell death.
Main Results:
- Successfully synthesized biocompatible graphene nanocarriers (in situ GIOPMPC) with well-distributed IONPs and polymers.
- Nanocarriers exhibited excellent water dispersibility and low cytotoxicity to thyroid cancer cells (IC50: 38.26 mg/mL).
- Doxorubicin-loaded nanocarriers effectively delivered the drug to thyroid cancer cells, inducing significant cytotoxicity through apoptosis, proliferation inhibition, and DNA damage.
Conclusions:
- The developed graphene-based nanocarriers are effective platforms for targeted doxorubicin delivery in thyroid cancer.
- The synthesis method offers a simplified approach using direct graphite.
- These nanocarriers demonstrate significant potential for developing advanced cancer therapeutics.
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