dc.contributor.author | Ogunc, Yüksel | |
dc.contributor.author | Demirel, Müzeyyen | |
dc.contributor.author | Yakar, Arzu | |
dc.contributor.author | Seller, Zerrin | |
dc.date.accessioned | 2019-10-19T14:03:03Z | |
dc.date.available | 2019-10-19T14:03:03Z | |
dc.date.issued | 2017 | |
dc.identifier.issn | 0265-2048 | |
dc.identifier.issn | 1464-5246 | |
dc.identifier.uri | https://dx.doi.org/10.1080/02652048.2017.1282549 | |
dc.identifier.uri | https://hdl.handle.net/11421/12487 | |
dc.description | WOS: 000396038300005 | en_US |
dc.description | PubMed ID: 28084127 | en_US |
dc.description.abstract | The objective of this study was to prepare the epsilon-viniferine and vincristine-loaded PLGA-b-PEG nanoparticle and to investigate advantages of these formulations on the cytotoxicity of HepG2 cells. Prepared nanoparticle has shown a homogeneous distribution with 113 +/- 0.43nm particle size and 0.323 +/- 0.01 polydispersity index. Zeta potential was determined as -35.03 +/- 1.0mV. The drug-loading percentages were 6.01 +/- 0.23 and 2.01 +/- 0.07 for epsilon-viniferine and vincristine, respectively. The cellular uptake efficiency of coumarin-6-loaded nanoparticles was increased up to 87.8% after 4h. Nanoparticles loaded with high concentrations of both drugs showed a cytotoxic effect on HepG2 cells, having the percentage of cell viability of between 43.23% and 47.37%. Unfortunately, the percentage of apoptotic cells after treated with drugs-loaded nanaoparticles (10.93%) was similar to free forms of drugs (12.1%) that might be due to low epsilon-viniferine release in biological pH at 24h. | en_US |
dc.description.sponsorship | Anadolu University [1406S313] | en_US |
dc.description.sponsorship | This work was funded by a grant from the Anadolu University (Project No. 1406S313). | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Taylor & Francis LTD | en_US |
dc.relation.isversionof | 10.1080/02652048.2017.1282549 | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Nanoparticle | en_US |
dc.subject | Plga-B-Peg | en_US |
dc.subject | Passive Targeting | en_US |
dc.subject | Epsilon-Viniferine | en_US |
dc.subject | Vincristine | en_US |
dc.title | Vincristine and epsilon-viniferine-loaded PLGA-b-PEG nanoparticles: pharmaceutical characteristics, cellular uptake and cytotoxicity | en_US |
dc.type | article | en_US |
dc.relation.journal | Journal of Microencapsulation | en_US |
dc.contributor.department | Anadolu Üniversitesi, Eczacılık Fakültesi, Biyokimya Anabilim Dalı | en_US |
dc.identifier.volume | 34 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.startpage | 38 | en_US |
dc.identifier.endpage | 46 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.contributor.institutionauthor | Demirel, Müzeyyen | |
dc.contributor.institutionauthor | Seller, Zerrin | |