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Nigella sativa oil entrapped polycaprolactone nanoparticles for leishmaniasis treatment

dc.contributor.authorAbamor, Emrah Sefik
dc.contributor.authorTosyali, Ozlem Ayse
dc.contributor.authorBagirova, Melahat
dc.contributor.authorAllahverdiyev, Adil
dc.date.accessioned2026-06-27T14:13:31Z
dc.date.issued2018
dc.description.abstractThis study is the first to investigate the antileishmanial activities of Nigella sativa oil (NSO) entrapped poly--caprolactone (PCL) nanoparticles on Leishmania infantum promastigotes and amastigotes in vitro. NSO molecules with variable initial doses of 50, 100, 150, and 200mg were successfully encapsulated into PCL nanoparticles identified as formulations NSO1, NSO2, NSO3, and NSO4, respectively. This process was characterised by scanning electron microscope, dynamic light scattering, Fourier transform infrared, encapsulation efficiency measurements, and release profile evaluations. The resulting synthetised nanoparticles had sizes ranging between 200 and 390nm. PCL nanoparticles encapsulated 98% to 80% of initial doses of NSO and after incubation released approximately 85% of entrapped oil molecules after 288h. All investigated formulations demonstrated strong antileishmanial effects on L. infantum promastigotes by inhibiting up to 90% of parasites after 192h. The tested formulations decreased infection indexes of macrophages in a range between 2.4- and 4.1-fold in contrast to control, thus indicating the strong anti-amastigote activities of NSO encapsulated PCL nanoparticles. Furthermore, NSO-loaded PCL nanoparticles showed immunomodulatory effects by increasing produced nitric oxide amounts within macrophages by 2-3.5-fold in contrast to use of free oil. The obtained data showed significant antileishmanial effects of NSO encapsulated PCL nanoparticles on L. infantum promastigotes and amastigotes.en
dc.description.urihttps://doi.org/10.1049/iet-nbt.2018.5115
dc.identifier.doi10.1049/iet-nbt.2018.5115
dc.identifier.eissn1751-875X
dc.identifier.endpage1026
dc.identifier.issn1751-8741
dc.identifier.issue8
dc.identifier.pubmed30964007
dc.identifier.startpage1018
dc.identifier.urihttps://hdl.handle.net/20.500.14981/58146
dc.identifier.volume12
dc.identifier.wos000451770900003
dc.language.isoeng
dc.publisherWILEY
dc.relation.ispartofIET NANOBIOTECHNOLOGY
dc.rightsopenAccess
dc.subjectantibacterial activity
dc.subjectdrug delivery systems
dc.subjectnanofabrication
dc.subjectnitrogen compounds
dc.subjectnanomedicine
dc.subjectmicroorganisms
dc.subjectcellular biophysics
dc.subjectdiseases
dc.subjectscanning electron microscopy
dc.subjectoils
dc.subjectpolymers
dc.subjectbiomedical materials
dc.subjectnanoparticles
dc.subjectencapsulation
dc.subjectFourier transform infrared spectra
dc.subjectencapsulation efficiency measurements
dc.subjectentrapped oil molecules
dc.subjectinvestigated formulations
dc.subjectNSO-loaded PCL nanoparticles
dc.subjectNigella sativa oil entrapped polycaprolactone nanoparticles
dc.subjectantileishmanial activities
dc.subjectpoly-epsilon-caprolactone nanoparticles
dc.subjectscanning electron microscope
dc.subjectDLS
dc.subjectFourier transform infrared
dc.subjectrelease profile evaluations
dc.subjectLeishmania infantum promastigotes
dc.subjectLeishmania infantum amastigotes
dc.subjectparasites
dc.subjectinfection
dc.subjectinfection indexes
dc.subjectmacrophages
dc.subjectimmunomodulatory effects
dc.subjecttime 288
dc.subject0 hour
dc.subjecttime 192
dc.subjectmass 50
dc.subject0 mg
dc.subjectmass 100
dc.subjectmass 150
dc.subjectmass 200
dc.subjectsize 200
dc.subject0 nm to 390
dc.subject0 nm
dc.subjectANTIMICROBIAL ACTIVITY
dc.subjectCONTROLLED-RELEASE
dc.subjectANTILEISHMANIAL ACTIVITY
dc.subjectCUTANEOUS LEISHMANIASIS
dc.subjectNITRIC-OXIDE
dc.subjectCELL-LINES
dc.subjectDELIVERY
dc.subjectDRUG
dc.subjectCYTOTOXICITY
dc.subjectSEED
dc.subjectBiochemistry & Molecular Biology
dc.subjectScience & Technology - Other Topics
dc.titleNigella sativa oil entrapped polycaprolactone nanoparticles for leishmaniasis treatment
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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