Development of hydrophobic reduced graphene oxide as a new efficient approach for photochemotherapy.
Seyyed Mojtaba MousaviFoo Wah LowSeyyed Alireza HashemiNurul Asma SamsudinMohammad ShakeriYulisa YusoffMansoor RahseparChin Wei LaiAziz BabapoorSadaf SoroshniaSu Mei GohSieh Kiong TiongNowshad AminPublished in: RSC advances (2020)
Nowadays, chemotherapy is one of the crucial and common therapies in the world. So far, it has been revealed to be highly promising, yet patients suffer from the consequences of severe negative medical dosages. In order to overcome these issues, the enhancement of photothermal chemotherapy with reduced graphene oxide (rGO) as a photothermal agent (PTA) is widely utilised in current medical technologies. This is due to its high near-infrared region (NIR) response, in vitro or in vivo organism biocompatibility, low risk of side effects, and effective positive results. Moreover, rGO not only has the ability to ensure that selective cancer cells have a higher mortality rate but can also improve the growth rate of recovering tissues that are untouched by necrosis and apoptosis. These two pathways are specific diverse modalities of cell death that are distinguished by cell membrane disruption and deoxyribonucleic acid (DNA) disintegration of the membrane via phosphatidylserine exposure in the absence of cell membrane damage. Therefore, this review aimed to demonstrate the recent achievements in the modification of rGO nanoparticles as a PTA as well as present a new approach for performing photochemotherapy in the clinical setting.
Keyphrases
- reduced graphene oxide
- gold nanoparticles
- cell death
- photodynamic therapy
- drug release
- healthcare
- oxidative stress
- ejection fraction
- end stage renal disease
- drug delivery
- locally advanced
- newly diagnosed
- cell cycle arrest
- cancer therapy
- gene expression
- prognostic factors
- cardiovascular events
- circulating tumor
- patient reported outcomes
- single molecule
- radiation therapy
- chronic kidney disease
- cardiovascular disease
- ionic liquid
- single cell
- endoplasmic reticulum stress
- squamous cell carcinoma
- coronary artery disease
- fluorescence imaging
- drug induced
- signaling pathway