Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/47454
Title: Investigation of in vitro biological activities of hollow mesoporous carbon nanoparticles bearing D-NMAPPD on human lung adenocarcinoma cells
Authors: Ugur N.
Harputlu E.
Sezer C.V.
Demirdogen R.E.
Ince M.
Unlu C.G.
Yurt F.
Keywords: Cytotoxicity
D-NMAPPD
Hollow mesoporous carbon nanoparticles
Lung cancer
1 (4' nitrophenyl) 2 (tetradecanoylamido) 1,3 propanediol
antineoplastic agent
carbon nanoparticle
ceramide derivative
hollow mesoporous carbon nanoparticle
unclassified drug
A-549 cell line
antineoplastic activity
antiproliferative activity
apoptosis
Article
biological activity
cell ultrastructure
cell viability
chromatin condensation
confocal microscopy
controlled study
drug cytotoxicity
drug release
field emission scanning electron microscopy
Fourier transform infrared spectroscopy
human
human cell
IC50
immobilization
in vitro study
lung adenocarcinoma
transmission electron microscopy
Publisher: Editions de Sante
Abstract: The uniformly dispersed hollow mesoporous carbon nanoparticles (HMCNPs) were successfully synthesized by hard-template methods, and D-NMAPPD (B13) was successfully loaded onto the nanoparticle surface for the first time. Structural properties of bare and B13 loaded HMCNPs (HMCNs-B-13) were investigated by Fourier Transform Infrared Spectroscopy (FT-IR), Field Emission-Scanning Electron Microscopy (FE-SEM), Thermal Gravimetric Analysis (TG). The amount of drug released was determined via in vitro drug release studies at 37 °C in SBF through UV–Vis spectrometric and thermal analyses. TG data revealed that the proportion of loaded B-13 was 33.60%. Their ability to induce apoptosis in cultures of A549 human lung adenocarcinoma cells was investigated, and the inhibitory effect of HMCNPs-B-13 on lung cancer cell proliferation was determined in vitro. The IC50 values determined after application periods of 24 and 48 h were found to be 16.13 ?g/mL and 12.96 ?g/mL, respectively. The role of HMCNPs-B-13 on the morphology and ultrastructure of A549 cells was also investigated by confocal microscopy and Transmission electron microscopy (TEM) studies. © 2021 Elsevier B.V.
URI: https://doi.org/10.1016/j.jddst.2021.102778
https://hdl.handle.net/11499/47454
ISSN: 1773-2247
Appears in Collections:Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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