Visible Pulsed Laser-Assisted Selective Killing of Cancer Cells with PVP-Capped Plasmonic Gold Nanostars.
Aniket MishraRafia InaamShunya OkamotoTakayuki ShibataTuhin Subhra SantraMoeto NagaiPublished in: Micromachines (2023)
A new generation of nanoscale photosensitizer agents has improved photothermal capabilities, which has increased the impact of photothermal treatments (PTTs) in cancer therapy. Gold nanostars (GNS) are promising for more efficient and less invasive PTTs than gold nanoparticles. However, the combination of GNS and visible pulsed lasers remains unexplored. This article reports the use of a 532 nm nanosecond pulse laser and polyvinylpyrrolidone (PVP)-capped GNS to kill cancer cells with location-specific exposure. Biocompatible GNS were synthesized via a simple method and were characterized under FESEM, UV-visible spectroscopy, XRD analysis, and particle size analysis. GNS were incubated over a layer of cancer cells that were grown in a glass Petri dish. A nanosecond pulsed laser was irradiated on the cell layer, and cell death was verified via propidium iodide (PI) staining. We assessed the effectiveness of single-pulse spot irradiation and multiple-pulse laser scanning irradiation in inducing cell death. Since the site of cell killing can be accurately chosen with a nanosecond pulse laser, this technique will help minimize damage to the cells around the target cells.
Keyphrases
- cell death
- cell cycle arrest
- cancer therapy
- photodynamic therapy
- blood pressure
- gold nanoparticles
- induced apoptosis
- high speed
- drug delivery
- single cell
- systematic review
- high resolution
- cell therapy
- oxidative stress
- single molecule
- randomized controlled trial
- drug release
- endoplasmic reticulum stress
- radiation therapy
- atomic force microscopy
- pi k akt
- cell proliferation
- mesenchymal stem cells
- drug induced
- plant growth