Effect of Artemisinin-Loaded Mesoporous Cerium-Doped Calcium Silicate Nanopowder on Cell Proliferation of Human Periodontal Ligament Fibroblasts.
Ioannis TsamesidisDimitrios GkiliopoulosGeorgia K PouroutzidouEvgenia LymperakiChrysanthi PapouliaKarine ReybierPierre PerioKonstantinos M ParaskevopoulosEleana KontonasakiAnna TheocharidouPublished in: Nanomaterials (Basel, Switzerland) (2021)
Ion doping has rendered mesoporous structures important materials in the field of tissue engineering, as apart from drug carriers, they can additionally serve as regenerative materials. The purpose of the present study was the synthesis, characterization and evaluation of the effect of artemisinin (ART)-loaded cerium-doped mesoporous calcium silicate nanopowders (NPs) on the hemocompatibility and cell proliferation of human periodontal ligament fibroblasts (hPDLFs). Mesoporous NPs were synthesized in a basic environment via a surfactant assisted cooperative self-assembly process and were characterized using Scanning Electron Microscopy (SEM), X-ray Fluorescence Spectroscopy (XRF), Fourier Transform Infrared Spectroscopy (FT-IR), X-ray Diffraction Analysis (XRD) and N2 Porosimetry. The loading capacity of NPs was evaluated using Ultrahigh Performance Liquid Chromatography/High resolution Mass Spectrometry (UHPLC/HRMS). Their biocompatibility was evaluated with the MTT assay, and the analysis of reactive oxygen species was performed using the cell-permeable ROS-sensitive probe 2',7'-dichlorodihydrofluorescein diacetate (H2DCFDA). The synthesized NPs presented a mesoporous structure with a surface area ranging from 1312 m2/g for undoped silica to 495 m2/g for the Ce-doped NPs, excellent bioactivity after a 1-day immersion in c-SBF, hemocompatibility and a high loading capacity (around 80%). They presented ROS scavenging properties, and both the unloaded and ART-loaded NPs significantly promoted cell proliferation even at high concentrations of NPs (125 μg/mL). The ART-loaded Ce-doped NPs with the highest amount of cerium slightly restricted cell proliferation after 7 days of culture, but the difference was not significant compared with the control untreated cells.
Keyphrases
- oxide nanoparticles
- cell proliferation
- electron microscopy
- high resolution mass spectrometry
- metal organic framework
- highly efficient
- quantum dots
- liquid chromatography
- high resolution
- reactive oxygen species
- tissue engineering
- drug delivery
- cell cycle
- endothelial cells
- cancer therapy
- cell death
- mass spectrometry
- ultra high performance liquid chromatography
- hiv infected
- wound healing
- single molecule
- pi k akt
- stem cells
- induced apoptosis
- cell therapy
- single cell
- energy transfer
- visible light
- mesenchymal stem cells
- emergency department
- antiretroviral therapy
- magnetic resonance imaging
- cell cycle arrest
- computed tomography
- signaling pathway
- bone marrow
- living cells
- dual energy
- drug induced
- plasmodium falciparum