Green Light-Triggerable Chemo-Photothermal Activity of Cytarabine-Loaded Polymer Carbon Dots: Mechanism and Preliminary In Vitro Evaluation.
Grazia Maria Letizia ConsoliMaria Laura GiuffridaStefania ZimboneLoredana FerreriLudovica MaugeriMichele PalmieriCristina SatrianoGiuseppe ForteSalvatore PetraliaPublished in: ACS applied materials & interfaces (2023)
Carbon-based nanostructures are attracting a lot of attention because of their very low toxicity, excellent visible light-triggered optical and photothermal properties, and intriguing applications. Currently, the development of multifunctional carbon-based nanostructures for a synergistic chemo-photothermal approach is a challenging topic for the advancement of cancer treatment. Here, we report an unprecedented example of photoresponsive carbon-based polymer dots (CPDs-PNM) obtained by a one-pot thermal process from poly( N -isopropylacrylamide) (PNIPAM) without using organic solvent and additional reagents. The CPDs-PNM nanostructures were characterized by spectroscopic techniques, transmission electron microscopy, and atomic force microscopy. The CPDs-PNM exhibited high photothermal conversion efficiency, lower critical solution temperature (LCST) behavior, and good cytarabine (arabinosyl cytosine, AraC) loading capacity (62.3%). The formation of a CPDs-PNM/AraC adduct and photothermal-controlled drug release, triggered by green light excitation, were demonstrated by spectroscopic techniques, and the drug-polymer interaction and drug release mechanism were well supported by modeling simulation calculations. The cellular uptake of empty and AraC-loaded CPDs-PNM was imaged by confocal laser scanning microscopy. In vitro experiments evidenced that CPDs-PNM did not affect the viability of neuroblastoma cells, while the CPDs-PNM/AraC adduct under light irradiation exhibited significantly higher toxicity than AraC alone by a combined chemo-photothermal effect.
Keyphrases
- drug release
- drug delivery
- cancer therapy
- photodynamic therapy
- high speed
- atomic force microscopy
- electron microscopy
- high resolution
- high dose
- oxidative stress
- molecular docking
- visible light
- optical coherence tomography
- single molecule
- working memory
- induced apoptosis
- cell cycle arrest
- low dose
- radiation induced
- mass spectrometry
- cell death
- high throughput
- radiation therapy
- cell proliferation
- density functional theory
- liquid chromatography
- single cell
- metal organic framework