» Articles » PMID: 32824495

Near-Infrared Radiation-Based Mild Photohyperthermia Therapy of Non-Melanoma Skin Cancer with PEGylated Reduced Nanographene Oxide

Overview
Publisher MDPI
Date 2020 Aug 23
PMID 32824495
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Using a one-step thermal reduction and non-covalent chemical functionalization process, PEGylated reduced nanographene oxide (rGOn-PEG) was produced from nanographene oxide (GOn) and characterized in terms of particle size, dispersion stability, chemistry, and photothermal properties, in view of its use for photothermal therapy (PTT) of non-melanoma skin cancer. GOn infrared spectrum presented more intense bands assigned to oxygen containing functional groups than observed for rGOn-PEG. GOn C/O ratio decreased more than 50% comparing with rGOn-PEG and nitrogen was present in the latter (N % = 20.6) due to introduction of PEG-NH. Thermogravimetric analysis allowed estimating the amount of PEG in rGOn-PEG to be of about 56.1%. Simultaneous reduction and PEGylation increased the lateral dimensions from 287 ± 139 nm to 521 ± 397 nm, as observed by transmission electron microscopy and dynamic light scattering. rGOn-PEG exhibited ≈13-fold higher absorbance in the near-infrared radiation (NIR) region, as compared to unmodified GOn. Low power (150 mW cm) NIR irradiation using LEDs resulted in rGOn-PEG heating up to 47 °C, which is within the mild PTT temperature range. PEGylation strongly enhanced the dispersibility of rGOn in physiological media (phosphate buffered saline, fetal bovine serum, and cell culture medium) and also improved the biocompatibility of rGOn-PEG, in comparison to GOn (25-250 μg mL). After a single NIR LED irradiation treatment of 30 min, a decrease of ≈38% in A-431 cells viability was observed for rGOn-PEG (250 μg mL). Together, our results demonstrate the potential of irradiating rGOn-PEG using lower energy, cheaper, smaller, and safer LEDs, as alternative to high power lasers, for NIR mild hyperthermia therapy of cancer, namely non-melanoma skin cancer.

Citing Articles

New MoS/Tegafur-Containing Pharmaceutical Formulations for Selective LED-Based Skin Cancer Photo-Chemotherapy.

Campos M, Silva F, Fernandes J, Santos S, Magalhaes F, Oliveira M Pharmaceutics. 2024; 16(3).

PMID: 38543254 PMC: 10974967. DOI: 10.3390/pharmaceutics16030360.


Innovative Topical Patches for Non-Melanoma Skin Cancer: Current Challenges and Key Formulation Considerations.

Kim S, Day C, Song Y, Holmes A, Garg S Pharmaceutics. 2023; 15(11).

PMID: 38004557 PMC: 10674480. DOI: 10.3390/pharmaceutics15112577.


Carbonaceous Nanomaterials for Phototherapy of Cancer.

Gupta T, Pawar B, Vasdev N, Pawar V, Kumar Tekade R Technol Cancer Res Treat. 2023; 22:15330338231186388.

PMID: 37461375 PMC: 10357070. DOI: 10.1177/15330338231186388.


Review article laser-induced hyperthermia on graphene oxide composites.

Gonzalez-Rodriguez L, Perez-Davila S, Lopez-Alvarez M, Chiussi S, Serra J, Gonzalez P J Nanobiotechnology. 2023; 21(1):196.

PMID: 37340410 PMC: 10280920. DOI: 10.1186/s12951-023-01956-6.


The Role of Graphene Oxide Nanocarriers in Treating Gliomas.

Wang B, Guo H, Xu H, Chen Y, Zhao G, Yu H Front Oncol. 2022; 12:736177.

PMID: 35155223 PMC: 8831729. DOI: 10.3389/fonc.2022.736177.


References
1.
Fadeel B, Bussy C, Merino S, Vazquez E, Flahaut E, Mouchet F . Safety Assessment of Graphene-Based Materials: Focus on Human Health and the Environment. ACS Nano. 2018; 12(11):10582-10620. DOI: 10.1021/acsnano.8b04758. View

2.
Vacchi I, Spinato C, Raya J, Bianco A, Menard-Moyon C . Chemical reactivity of graphene oxide towards amines elucidated by solid-state NMR. Nanoscale. 2016; 8(28):13714-13721. DOI: 10.1039/c6nr03846h. View

3.
Hegyi G, Szigeti G, Szasz A . Hyperthermia versus Oncothermia: Cellular Effects in Complementary Cancer Therapy. Evid Based Complement Alternat Med. 2013; 2013:672873. PMC: 3638606. DOI: 10.1155/2013/672873. View

4.
Robinson J, Tabakman S, Liang Y, Wang H, Sanchez Casalongue H, Vinh D . Ultrasmall reduced graphene oxide with high near-infrared absorbance for photothermal therapy. J Am Chem Soc. 2011; 133(17):6825-31. DOI: 10.1021/ja2010175. View

5.
Kim H, Lee D, Kim J, Kim T, Kim W . Photothermally triggered cytosolic drug delivery via endosome disruption using a functionalized reduced graphene oxide. ACS Nano. 2013; 7(8):6735-46. DOI: 10.1021/nn403096s. View