WS 2 /Polyethylene Glycol Nanostructures for Ultra-Efficient MCF-7 Cancer Cell Ablation and Electrothermal Therapy.
Maria Prisca MeivitaSophia S Y ChanShao Xiang GoDenise LeeNatasa BajalovicDesmond K LokePublished in: ACS omega (2022)
Developing novel nanostructures and advanced nanotechnologies for cancer treatment has attracted ever-increasing interest. Electrothermal therapy offers many advantages such as high efficiency and minimal invasiveness, but finding a balance between increasing stability of the nanostructure state and, at the same time, enhancing the nanostructure biodegradability presents a key challenge. Here, we modulate the biodegradation process of two-dimensional-material-based nanostructures by using polyethylene glycol (PEG) via nanostructure disrupt-and-release effects. We then demonstrate the development of a previously unreported alternating current (AC) pulse WS 2 /PEG nanostructure system for enhancing therapeutic performance. A decrease in cell viability of ∼42% for MCF-7 cells with WS 2 /PEG was achieved, which is above an average of ∼25% for current electrothermal-based therapeutic methods using similar energy densities, as well as degradation time of the WS 2 of ∼1 week, below an average of ∼3.5 weeks for state-of-the-art nanostructure-based systems in physiological media. Moreover, the incubation time of MCF-7 cells with WS 2 /PEG reached ∼24 h, which is above the average of ∼4.5 h for current electrothermal-based therapeutic methods and with the use of the amount of time harnessed to incubate the cells with nanostructures before applying a stimulus as a measure of incubation time. Material characterizations further disclose the degradation of WS 2 and the grafting of PEG on WS 2 surfaces. These WS 2 -based systems offer strong therapeutic performance and, simultaneously, maintain excellent biodegradability/biocompatibility, thus providing a promising route for the ablation of cancer.
Keyphrases
- induced apoptosis
- drug delivery
- cell cycle arrest
- high efficiency
- breast cancer cells
- squamous cell carcinoma
- endoplasmic reticulum stress
- cell death
- oxidative stress
- clinical trial
- escherichia coli
- staphylococcus aureus
- randomized controlled trial
- bone marrow
- young adults
- pseudomonas aeruginosa
- cystic fibrosis
- replacement therapy
- smoking cessation
- atrial fibrillation
- cell therapy
- preterm birth