Repositorio Dspace

Designing of SiO2 mesoporous nanoparticles loaded with mometasone furoate for potential nasal drug delivery: Ex vivo evaluation and determination of pro-inflammatory interferon and interleukin mRNA expression

Mostrar el registro sencillo del ítem

dc.rights.license CC BY eng
dc.contributor.author Mehmood, Y. cze
dc.contributor.author Shahid, H. cze
dc.contributor.author Barkat, K. cze
dc.contributor.author Ibraheem, M. cze
dc.contributor.author Riaz, H. cze
dc.contributor.author Badshah, S.F. cze
dc.contributor.author Chopra, H. cze
dc.contributor.author Sharma, R. cze
dc.contributor.author Nepovimová, Eugenie cze
dc.contributor.author Kuča, Kamil cze
dc.contributor.author Valis, M. cze
dc.contributor.author Emran, T.B. cze
dc.date.accessioned 2025-12-05T11:50:26Z
dc.date.available 2025-12-05T11:50:26Z
dc.date.issued 2023 eng
dc.identifier.issn 2296-634X eng
dc.identifier.uri http://hdl.handle.net/20.500.12603/1689
dc.description.abstract The main objective of the current research work was to synthesize mesoporous silica nanoparticles for controlled delivery of mometasone furoate for potential nasal delivery. The optimized sol–gel method was used for the synthesis of mesoporous silica nanoparticles. Synthesized nanoparticles were processed through Zeta sizer, SEM, TEM, FTIR, TGA, DSC, XRD, and BET analysis for structural characterization. The in vitro dissolution test was performed for the inclusion compound, while the Franz diffusion experiment was performed for permeability of formulation. For the determination of expression levels of anti-inflammatory cytokines IL-4 and IL-5, RNA extraction, reverse transcription, and polymerase chain reaction (RT-PCR) were performed. The MTT assay was also performed to determine cell viability. Synthesized and functionalized mesoporous silica nanoparticles showed controlled release of drugs. FT-IR spectroscopy confirmed the presence of the corresponding functional groups of drugs within mesoporous silica nanoparticles. Zeta sizer and thermal analysis confirmed the delivery system was in nano size and thermally stable. Moreover, a highly porous system was observed during SEM and TEM evaluation, and further it was confirmed by BET analysis. Greater cellular uptake with improved permeability characteristics was also observed. As compared to the crystalline drug, a significant improvement in the dissolution rate was observed. It was concluded that stable mesoporous silica nanoparticles with significant porosity were synthesized, efficiently delivering the loaded drug without any toxic effect. Copyright © 2023 Mehmood, Shahid, Barkat, Ibraheem, Riaz, Badshah, Chopra, Sharma, Nepovimova, Kuca, Valis and Emran. eng
dc.format p. "Article number: 1026477" eng
dc.language.iso eng eng
dc.publisher Frontiers Media S.A. eng
dc.relation.ispartof Frontiers in Cell and Developmental Biology, volume 10, issue: January eng
dc.subject controlled release eng
dc.subject drug delivery eng
dc.subject ex vivo study eng
dc.subject mesoporous silica nanoparticles eng
dc.subject nasal spray eng
dc.title Designing of SiO2 mesoporous nanoparticles loaded with mometasone furoate for potential nasal drug delivery: Ex vivo evaluation and determination of pro-inflammatory interferon and interleukin mRNA expression eng
dc.type article eng
dc.identifier.obd 43879634 eng
dc.identifier.doi 10.3389/fcell.2022.1026477 eng
dc.publicationstatus postprint eng
dc.peerreviewed yes eng
dc.source.url https://www.frontiersin.org/articles/10.3389/fcell.2022.1026477/full cze
dc.relation.publisherversion https://www.frontiersin.org/articles/10.3389/fcell.2022.1026477/full eng
dc.rights.access Open Access eng


Ficheros en el ítem

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem

Buscar en DSpace


Listar

Mi cuenta