A comparative study of cytotoxicity of PPG and PEG surface-modified 2-D Ti3C2 mxene flakes on human cancer cells and their photothermal response

• Main Authors: Anwar, A. (Author), Aslfattahi, N. (Author), Mohan, G. (Author), Rashid, B. (Author), Saidur, R. (Author), Shahabuddin, S. (Author), Sridewi, N. (Author)
• Format: Article
• Language: English
• Published: MDPI AG 2021
• Series: Materials
• Subjects: Anticancer; Anti-cancer agents; Anticancer potentials; Biomedical activity; Cell culture; Cells; Chemical modification; Comparative studies; Cytotoxicity; Elemental compositions; Fourier transform infrared spectroscopy; Light absorption; Metabolism; Morphology; MXene; PEG; Photothermal response; Polypropylene glycol; Polypropylene oxides; Polypropylenes; PPG; PTT; Surface morphology; Synthesis (chemical); Titanium compounds; Toxicity; Ultraviolet visible spectroscopy; UV-vis spectroscopy; Wet etching
• Online Access: View Fulltext in Publisher; View in Scopus

 The MXenes are a novel family of 2-D materials with promising biomedical activity, however, their anticancer potential is still largely unexplored. In this study, a comparative cytotoxicity investigation of Ti3C2 MXenes with polypropylene glycol (PPG), and polyethylene glycol (PEG) surface-modified 2-D Ti3C2 MXene flakes has been conducted towards normal and cancerous human cell lines. The wet chemical etching method was used to synthesize MXene followed by a simple chemical mixing method for surface modification of Ti3C2 MXene with PPG and PEG molecules. SEM and XRD analyses were performed to examine surface morphology and elemental composition, respectively. FTIR and UV-vis spectroscopy were used to confirm surface modification and light absorption, respectively. The cell lines used to study the cytotoxicity of MXene and surface-modified MXenes in this study were normal (HaCaT and MCF-10A) and cancerous (MCF-7 and A375) cells. These cell lines were also used as controls (without exposure to study material and irradiation) to measure their baseline cell viability under the same lab environment. The surface-modified MXenes exhibited a sharp reduction in cell viability towards both normal (HaCaT and MCF-10A) and cancerous (MCF-7 and A375) cells but cytotoxicity was more pronounced towards cancerous cell lines. This may be due to the difference in cell metabolism and the occurrence of high pre-existing levels of reactive oxygen species (ROS) within cancerous cells. The highest toxicity towards both normal and cancerous cell lines was observed with PEGylated MXenes followed by PPGylated and bare MXenes. The normal cell’s viability was barely above 70% threshold with 250 mg/L PEGylated MXene concentration whereas PPGylated and bare MXene were less toxic towards normal cells, even at 500 mg/L concentration. Moreover, the toxicity was found to be directly related to the type of cell lines. In general, the HaCaT cell line exhibited the lowest toxicity while toxicity was highest in the case of the A375 cell line. The photothermal studies revealed high photo response for PEGylated MXene followed by PPGylated and bare MXenes. However, the PPGylated MXene’s lower cytotoxicity towards normal cells while comparable toxicity towards malignant cells as compared to PEGylated MXenes makes the former a relatively safe and effective anticancer agent. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.