One-Pot Synthesis of Luminescent and Photothermal Carbon Boron-Nitride Quantum Dots Exhibiting Cell Damage Protective Effects.
Grazia M L ConsoliLudovica MaugeriNicolò MussoAntonino GulinoLuisa D'UrsoPaolo BonacciGianpiero BuscarinoGiuseppe ForteSalvatore PetraliaPublished in: Advanced healthcare materials (2024)
Zero-dimensional boron nitride quantum dots (BNQDs) are arousing interest for their versatile optical, chemical, and biochemical properties. Introducing carbon contents in BNQDs nanostructures is a great challenge to modulate their physicochemical properties. Among the carbon moieties, phenolic groups have attracted attention for their biochemical properties and phenol-containing nanomaterials are showing great promise for biomedical applications. Herein, the first example of direct synthesis of water dispersible BNQDs exposing phenolic and carboxylic groups is presented. The carbon-BNQDs are prepared in a single-step by solvent-assisted reaction of urea with boronic reagents and are characterized by optical absorption, luminescence, Raman, Fourier transform infrared and NMR spectroscopy, X-ray photoelectron spectroscopy, dynamic light scattering, and atomic force microscopy. The carbon-BNQDs exhibit nanodimension, stability, high photothermal conversion efficiency, pH-responsive luminescence and Z-potential. The potential of the carbon-BNQDs to provide photothermal materials in solid by embedding in agarose substrate is successfully investigated. The carbon-BNQDs exhibit biocompatibility on colorectal adenocarcinoma cells (Caco-2) and protective effects from chemical and oxidative stress on Caco-2, osteosarcoma (MG-63), and microglial (HMC-3) cells. Amplicon mRNA-seq analyses for the expression of 56 genes involve in oxidative-stress and inflammation are performed to evaluate the molecular events responsible for the cell protective effects of the carbon-BNQDs.
Keyphrases
- quantum dots
- oxidative stress
- induced apoptosis
- atomic force microscopy
- high resolution
- single cell
- high speed
- sensitive detection
- squamous cell carcinoma
- cancer therapy
- drug delivery
- dna damage
- single molecule
- cell therapy
- ischemia reperfusion injury
- magnetic resonance imaging
- genome wide
- energy transfer
- signaling pathway
- cell cycle arrest
- stem cells
- endoplasmic reticulum stress
- poor prognosis
- rna seq
- cell proliferation
- inflammatory response
- working memory
- risk assessment
- big data
- heat shock
- mass spectrometry
- deep learning
- artificial intelligence
- human health