Probing Internalization Effects and Biocompatibility of Ultrasmall Zirconium Metal-Organic Frameworks UiO-66 NP in U251 Glioblastoma Cancer Cells.
Cataldo ArcuriLorenzo MonarcaFrancesco RagoneseCarmen MeccaStefano BruscoliStefano GiovagnoliRosario DonatoOxana BereshchenkoBernard FiorettiFerdinando CostantinoPublished in: Nanomaterials (Basel, Switzerland) (2018)
The synthesis of ultrasmall UiO-66 nanoparticles (NPs) with an average size of 25 nm, determined by X-ray powder diffraction and electron microscopies analysis, is reported. The NPs were stabilized in water by dialyzing the NP from the DMF used for the synthesis. DLS measurements confirmed the presence of particles of 100 nm, which are spherical aggregates of smaller particles of 20⁻30 nm size. The NP have a BET surface area of 700 m²/g with an external surface area of 300 m²/g. UiO-66_N (UiO-66 nanoparticles) were loaded with acridine orange as fluorescent probe. UV-vis spectroscopy analysis revealed no acridine loss after 48 h of agitation in simulated body fluid. The biocompatibility of UiO-66_N was evaluated in human glioblastoma (GBM) cell line U251, the most malignant (IV grade of WHO classification) among brain tumors. In U251 cells, UiO-66_N are inert since they do not alter the cell cycle, the viability, migration properties, and the expression of kinases involved in cancer cell growth. The internalization process was evident after a few hours of incubation. After 24 h, UiO-66_N@Acr (UiO-66_N loaded with acridine orange) were detectable around the nuclei of the cells. These data suggest that small UiO-66 are biocompatible NP and could represent a potential carrier for drug delivery in glioblastoma therapies.
Keyphrases
- metal organic framework
- drug delivery
- cell cycle
- induced apoptosis
- fluorescent probe
- cell proliferation
- photodynamic therapy
- high resolution
- cancer therapy
- cell cycle arrest
- living cells
- papillary thyroid
- risk assessment
- magnetic resonance
- magnetic resonance imaging
- cell death
- single molecule
- computed tomography
- signaling pathway
- wound healing
- endoplasmic reticulum stress
- electronic health record
- squamous cell carcinoma
- big data
- long non coding rna
- oxidative stress
- electron microscopy
- artificial intelligence
- lymph node metastasis
- contrast enhanced