Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/9491
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dc.contributor.authorNur, S.G.-
dc.contributor.authorBuket, O.-
dc.contributor.authorSezgi, K.-
dc.contributor.authorCagdas, A.-
dc.contributor.authorCansu, A.-
dc.contributor.authorGuliz, A.-
dc.contributor.authorHabibe, Y.-
dc.date.accessioned2019-08-16T13:02:02Z
dc.date.available2019-08-16T13:02:02Z
dc.date.issued2016-
dc.identifier.issn1871-5206-
dc.identifier.urihttps://hdl.handle.net/11499/9491-
dc.identifier.urihttps://doi.org/10.2174/1871520616666160101120040-
dc.description.abstractThe objective of the study was to investigate the cytotoxic and apoptotic effects of Methotrexate (MTX)-loaded chitosan (CS) on LNCaP prostate cancer cell line in vitro. For this purpose, CS nanoparticles (NPs) were synthesized through ionic gelation method and MTX was loaded into the carrier with encapsulation. SEM images of the CS NPs have revealed that they have size of about 85 nm in mono-disperse manner. Drug loading yield was found to be 95.7 % with 470 µg drug/mg NP loading capacity. In vitro drug release study showed that MTX was released in a controlled manner. Cell viability was detected by using trypan blue dye exclusion test and WST-1 cell proliferation assay was performed to show cytotoxic effects of the CS, the MTX and the MTX-loaded NP. IC50 values of CS, MTX and MTX-loaded NPs were assigned from the cell survival plot and were determined as 67.18 µM, 20.21 µM and 2.94 µM at the 72nd hour, respectively. As for apoptosis analysis results, following to MTX-loaded CS treatment of LNCAP cells, apoptotic cell percent was detected as 39.3 % at the 72nd hour, that is, MTX-loaded CS induces 1.85-fold increase in apoptotic cell percent in comparison with that of MTX- induced apoptosis. © 2016 Bentham Science Publishers.en_US
dc.language.isoenen_US
dc.publisherBentham Science Publishers B.V.en_US
dc.relation.ispartofAnti-Cancer Agents in Medicinal Chemistryen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectApoptosisen_US
dc.subjectChitosan nanoparticlesen_US
dc.subjectCytotoxicityen_US
dc.subjectLNCaP cell lineen_US
dc.subjectMethotrexate deliveryen_US
dc.subjectchitosan derivativeen_US
dc.subjectmethotrexateen_US
dc.subjectnanoparticleen_US
dc.subjectapoptosisen_US
dc.subjectArticleen_US
dc.subjectcell proliferation assayen_US
dc.subjectcell viability assayen_US
dc.subjectcentrifugationen_US
dc.subjectclinical evaluationen_US
dc.subjectcomparative studyen_US
dc.subjectcontrolled studyen_US
dc.subjectcytotoxicityen_US
dc.subjectdrug releaseen_US
dc.subjectdrug synthesisen_US
dc.subjecthumanen_US
dc.subjecthuman cellen_US
dc.subjecthydrodynamicsen_US
dc.subjectIC50en_US
dc.subjectnanoencapsulationen_US
dc.subjectprostate canceren_US
dc.titleSynthesis of methotrexate loaded chitosan nanoparticles and in vitro evaluation of the potential in treatment of prostate canceren_US
dc.typeArticleen_US
dc.identifier.volume16en_US
dc.identifier.issue8en_US
dc.identifier.startpage1038
dc.identifier.startpage1038en_US
dc.identifier.endpage1042en_US
dc.identifier.doi10.2174/1871520616666160101120040-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid26721835en_US
dc.identifier.scopus2-s2.0-84981541469en_US
dc.identifier.wosWOS:000382250000009en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairetypeArticle-
item.fulltextNo Fulltext-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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