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dc.contributor.authorAlpdemir, Sukran
dc.contributor.authorVural, Tayfun
dc.contributor.authorKara, Goknur
dc.contributor.authorBayram, Cem
dc.contributor.authorHaberal, Erdem
dc.contributor.authorDenkbas, Emir Baki
dc.date.accessioned2021-04-28T06:29:21Z
dc.date.available2021-04-28T06:29:21Z
dc.date.issued2020
dc.identifier.issn1751-8741en_US
dc.identifier.urihttps://ietresearch.onlinelibrary.wiley.com/doi/pdfdirect/10.1049/iet-nbt.2020.0139
dc.identifier.urihttp://hdl.handle.net/11727/5785
dc.description.abstractThis study aimed to develop sorafenib loaded magnetic microspheres for the treatment of hepatocellular carcinoma. To achieve this goal, superparamagnetic iron oxide nanoparticles (SPIONs) were synthesised and encapsulated in alginate microspheres together with an antineoplastic agent, sorafenib. In the study, firstly SPIONs were synthesised and characterised by dynamic light scattering, energy-dispersive X-ray spectroscopy, and scanning electron microscopy. Then, alginate-SPIONs microspheres were developed, and further characterised by electron spin resonance spectrometer and vibrating sample magnetometer. Besides the magnetic properties of SPIONs, alginate microspheres with SPIONs were also found to have magnetic properties. The potential use of microspheres in hyperthermia treatment was then investigated and an increase of about 4 degrees C in the environment was found out. Drug release studies and cytotoxicity tests were performed after sorafenib was encapsulated into the magnetic microspheres. According to release studies, sorafenib has been released from microspheres for 8 h. Cytotoxicity tests showed that alginate-SPION-sorafenib microspheres were highly effective against cancerous cells and promising for cancer therapy.en_US
dc.language.isoengen_US
dc.relation.isversionof10.1049/iet-nbt.2020.0139en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectdrug delivery systemsen_US
dc.subjectdrugsen_US
dc.subjectnanofabricationen_US
dc.subjectmagnetic particlesen_US
dc.subjectiron compoundsen_US
dc.subjectscanning electron microscopyen_US
dc.subjecthyperthermiaen_US
dc.subjectbiomedical materialsen_US
dc.subjectencapsulationen_US
dc.subjectnanoparticlesen_US
dc.subjectlight scatteringen_US
dc.subjectnanomagneticsen_US
dc.subjectcellular biophysicsen_US
dc.subjecttoxicologyen_US
dc.subjectcanceren_US
dc.subjectnanomedicineen_US
dc.subjectsuperparamagnetismen_US
dc.subjectnanocompositesen_US
dc.subjectmagnetometryen_US
dc.subjectparamagnetic resonanceen_US
dc.subjectX-ray chemical analysisen_US
dc.subjectsorafenib loaded alginate microspheresen_US
dc.subjecthepatocellular carcinoma treatmenten_US
dc.subjectsorafenib loaded magnetic microspheresen_US
dc.subjectsuperparamagnetic iron oxide nanoparticlesen_US
dc.subjectdynamic light scatteringen_US
dc.subjectenergy-dispersive X-ray spectroscopyen_US
dc.subjectscanning electron microscopyen_US
dc.subjectelectron spin resonance spectrometeren_US
dc.subjectvibrating sample magnetometeren_US
dc.subjecthyperthermia treatmenten_US
dc.subjectdrug releaseen_US
dc.subjectalginate-SPION-sorafenib microspheresen_US
dc.subjectantineoplastic agenten_US
dc.subjectcytotoxicity testsen_US
dc.subjectcancerous cellsen_US
dc.subjecttime 8en_US
dc.subject0 houren_US
dc.subjectFe3O4en_US
dc.titleMagnetically responsive, sorafenib loaded alginate microspheres for hepatocellular carcinoma treatmenten_US
dc.typearticleen_US
dc.relation.journalIET NANOBIOTECHNOLOGYen_US
dc.identifier.volume14en_US
dc.identifier.issue7en_US
dc.identifier.startpage617en_US
dc.identifier.endpage622en_US
dc.identifier.wos000577098100011en_US
dc.identifier.scopus2-s2.0-85092430830en_US
dc.contributor.pubmedID33010138en_US
dc.contributor.orcID0000-0003-2788-550Xen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.contributor.researcherIDABC-8833-2020en_US


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