Poly(ε-caprolactone)-poly(ethylene glycol) Tri-Block Copolymer as Quercetin Delivery System for Human Colorectal Carcinoma Cells: Synthesis, Characterization and In Vitro Study.
Nancy FerrentinoMaria Preziosa RomanoSilvia ZappavignaMarianna AbateVitale Del VecchioDario RomanoChiara GerminarioCelestino GrifaRosanna FilosaDaniela PappalardoPublished in: Polymers (2023)
Quercetin is a hydrophobic molecule with short blood circulation times and instability. The development of a nano-delivery system formulation of quercetin may increase its bioavailability, resulting in greater tumor suppressing effects. Triblock ABA type polycaprolactone-polyethylenglycol- polycaprolactone (PCL-PEG-PCL) copolymers have been synthetized using ring-opening polymerization of caprolactone from PEG diol. The copolymers were characterized by nuclear magnetic resonance (NMR), diffusion-ordered NMR spectroscopy (DOSY), and gel permeation chromatography (GPC). The triblock copolymers self-assembled in water forming micelles consisting of a core of biodegradable polycaprolactone (PCL) and a corona of polyethylenglycol (PEG). The core-shell PCL-PEG-PCL nanoparticles were able to incorporate quercetin into the core. They were characterized by dynamic light scattering (DLS) and NMR. The cellular uptake efficiency of human colorectal carcinoma cells was quantitatively determined by flow cytometry using nanoparticles loaded with Nile Red as hydrophobic model drug. The cytotoxic effect of quercetin-loaded nanoparticles was evaluated on HCT 116 cells, showing promising results.
Keyphrases
- drug delivery
- magnetic resonance
- cancer therapy
- drug release
- tissue engineering
- flow cytometry
- endothelial cells
- cell cycle arrest
- induced pluripotent stem cells
- pluripotent stem cells
- mass spectrometry
- high resolution
- induced apoptosis
- magnetic resonance imaging
- ionic liquid
- signaling pathway
- cell death
- high speed
- tandem mass spectrometry
- cell proliferation
- arabidopsis thaliana
- liquid chromatography
- contrast enhanced
- high performance liquid chromatography
- drug induced
- adverse drug
- pi k akt