6533b858fe1ef96bd12b5a6a
RESEARCH PRODUCT
Natural payload delivery of the doxorubicin anticancer drug from boron nitride oxide nanosheets
Eric DuvergerFabien PicaudPhilippe MieleSebastien BalmeMikhael Bechelanysubject
General Physics and Astronomy02 engineering and technologyMolecular dynamics010402 general chemistry01 natural sciences[SPI.MAT]Engineering Sciences [physics]/MaterialsCell membranechemistry.chemical_compoundmedicinepolycyclic compoundsTime-dependent density functional theoryMolecule[CHIM]Chemical SciencesDoxorubicin[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/MicroelectronicsBoron nitride oxide nanosheetsNanosheet[SPI.ACOU]Engineering Sciences [physics]/Acoustics [physics.class-ph]Therapeutic agentsChemistrytechnology industry and agricultureSurfaces and InterfacesGeneral ChemistryTime-dependent density functional theory021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesSurfaces Coatings and FilmsSolventmedicine.anatomical_structureBoron nitrideDrug deliveryBiophysics0210 nano-technologymedicine.drugdescription
International audience; We studied the behavior of doxorubicin (DOX; an anticancer drug) molecules loaded on a boron nitride oxide nanosheet (BNO-NS) using the density functional theory (DFT), time-dependent density functional theory (TDDFT), and molecular dynamic (MD) simulation methods. We found that DOX molecules in pi-pi or covalent interaction with BNO-NS preserve their optical properties in water. Moreover, the BNO-NS vector allowed stabilizing the DOX molecules on a cellular membrane contrary to isolated DOX that randomly moved in the solvent box without any interaction with the cell membrane. From these results, we conclude that hydrophilic BNO-NS represents a good candidate for DOX molecule transport and stabilization near a cell membrane. In this drug delivery system, the choice of BNO-NS as nanovector is important because it allows delivering an elevated therapeutic dose directly on the cancer cell target without hindrance of the DOX payload.
year | journal | country | edition | language |
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2019-05-01 |