Comparison of intestinal permeability of nebivolol hydrochloride loaded solid lipid nanoparticles with commercial nebivolol tablet

dc.contributor.authorÜstündağ-Okur, Neslihan
dc.contributor.authorYurdasiper, Aysu
dc.contributor.authorKaynak, Mustafa Sinan
dc.contributor.authorGökçe, Evren Homan
dc.date.accessioned2021-11-10T09:24:59Z
dc.date.available2021-11-10T09:24:59Z
dc.date.issued2018
dc.departmentİnönü Üniversitesien_US
dc.description.abstractAbstract: The oral application of drugs is the most popular route for achieving systemic effects, nevertheless, it is limited by difficulties related to physicochemical properties of the drug. Solid lipid nanoparticles (SLNs) are appealing extensive notice because of showing increased solubility and improved oral bioavailability via different mechanisms. The aim of the study is to compare and peruse the in-situ permeation of nebivolol (NBV) loaded SLN and its commercial tablet formulation used for the treatment of hypertension. For this aim Single-Pass Intestinal Perfusion (SPIP) method was used for in-situ permeation studies. NBV loaded SLNs were prepared and modified with polyethylene glycol (PEG). In order to prepare SLNs by homogenization technique, compritol, lecithin and poloxamer were chosen. Particle sizes of blank and loaded SLN were 213.4±17.5 and 264.1±18.8 nm, respectively with polydispersity index values of approximately 0.3 for each. NBV loading resulted in positive electrical charge on SLNs. The encapsulation efficiency was 98.04±0.2 %. Permeability coefficient values were tripled when NBV was incorporated in SLNs and doubled when pure NBV was given separately with a blank SLN. PEG modified SLN can be used to enhance oral absorption of NBV, and SLNs alone can be used as permeation enhancer in oral drug delivery..en_US
dc.identifier.citationGÖKÇE E. H,KAYNAK M. S,YURDASİPER A,ÜSTÜNDAĞ-OKUR N (2018). Comparison of intestinal permeability of nebivolol hydrochloride loaded solid lipid nanoparticles with commercial nebivolol tablet. Marmara Pharmaceutical Journal, 22(4), 578 - 586. Doi: 10.12991/jrp.2018.100en_US
dc.identifier.doi10.12991/jrp.2018.100en_US
dc.identifier.endpage586en_US
dc.identifier.issn1309-0801
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-85056575323en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage578en_US
dc.identifier.trdizinid382806en_US
dc.identifier.urihttps://doi.org/10.12991/jrp.2018.100
dc.identifier.urihttps://hdl.handle.net/11616/43093
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/382806
dc.identifier.volume22en_US
dc.identifier.wosWOS:000458080300013en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakTR-Dizinen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.relation.ispartofMarmara Pharmaceutical Journalen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleComparison of intestinal permeability of nebivolol hydrochloride loaded solid lipid nanoparticles with commercial nebivolol tableten_US
dc.typeArticleen_US

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