نمایش پرونده ساده آیتم

dc.contributor.authorNakhlband, A
dc.contributor.authorEskandani, M
dc.contributor.authorSaeedi, N
dc.contributor.authorGhafari, S
dc.contributor.authorOmidi, Y
dc.contributor.authorBarar, J
dc.contributor.authorGarjani, A
dc.date.accessioned2018-08-26T09:00:45Z
dc.date.available2018-08-26T09:00:45Z
dc.date.issued2018
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/54940
dc.description.abstractOxidative stress possesses a key role in the onset and development of cardiovascular diseases (CVDs), thus it can be an efficient target to tackle such ailment. Marrubiin, a bioactive diterpene, is a potent antioxidant against oxidative stress. Herein, we aimed to formulate marrubiin loaded solid lipid nanoparticles (SLNs) to improve its pharmacokinetics and bioavailability and also to investigate free drug and formulation's protective impact against intracellular reactive oxygen species (ROS) generation in HUVECs. Marrubiin-SLNs were formulated using hot homogenization/solidification method and then were subjected to physicochemical characterizations, i.e. size, zeta potential, morphology, polydispersity index (PDI), encapsulation efficiency (% EE), drug loading/content and physical stability assessments. MTT assay was performed to study the cytotoxicity of the intact and SLN incorporated marrubiin on HUVECs. Further, the antioxidant property of marrubiin and formulations was evaluated using DPPH radical scavenging assay and their protective effect against TNF-? induced oxidative stress was assessed by the means of intracellular ROS assessment, and also apoptosis/necrosis, cell cycle, and DNA fragmentation assays. Electron microscopy analysis showed spherical monodispersed SLNs with the size less than 100 nm, particle/zeta size analyses also approved the size of particles with a zeta potential of ?1.28 آ± 0.17 mV. Results also showed high EE (98%), drug loading (31.74 mg/g) with 3.15% drug content. In vitro release studies revealed about 90% of marrubiin cumulative release during 24 h. The stability of marrubiin-SLNs in terms of size, zeta potential, polydispersity index, EE and drug leakage was approved. Marrubiin antioxidant stability after formulation was approved by DPPH analysis. MTT cell survival assay showed no significant cytotoxicity after 24 h and 48 h. Intracellular ROS detection assay revealed that marrubiin and marrubiin-SLNs, play protective effect against TNF-? induced oxidative stress in HUVECs which was further approved by apoptosis assessment. Conclusively, based on our findings, marrubiin nanoparticles are proposed as a preventive/therapeutic remedy against disorders elicited by increased levels of intracellular ROS in CVDs. é 2018
dc.language.isoEnglish
dc.relation.ispartofColloids and Surfaces B: Biointerfaces
dc.subjectAntioxidants
dc.subjectAssays
dc.subjectBiochemistry
dc.subjectCardiology
dc.subjectCell death
dc.subjectControlled drug delivery
dc.subjectDiseases
dc.subjectEncapsulation
dc.subjectEndothelial cells
dc.subjectHomogenization method
dc.subjectNanoparticles
dc.subjectOxidative stress
dc.subjectParticle size analysis
dc.subjectPolydispersity
dc.subjectSystem stability
dc.subjectTargeted drug delivery
dc.subjectZeta potential
dc.subjectCardio-vascular disease
dc.subjectCardioprotection
dc.subjectDNA damages
dc.subjectHot homogenization/solidification method
dc.subjectIntracellular ROS
dc.subjectMarrubiin
dc.subjectSolid lipid nanoparticles
dc.subjectDrug delivery
dc.subjectditerpene
dc.subjectmarrubiin
dc.subjectreactive oxygen metabolite
dc.subjectsolid lipid nanoparticle
dc.subjecttumor necrosis factor
dc.subjectunclassified drug
dc.subjectantioxidant activity
dc.subjectapoptosis
dc.subjectArticle
dc.subjectcell cycle assay
dc.subjectcell death
dc.subjectcontrolled study
dc.subjectcytotoxicity
dc.subjectdispersity
dc.subjectDNA fragmentation assay
dc.subjectDPPH radical scavenging assay
dc.subjectdrug bioavailability
dc.subjectdrug effect
dc.subjectdrug release
dc.subjectdrug stability
dc.subjectelectron microscopy
dc.subjectheart protection
dc.subjecthuman
dc.subjecthuman cell
dc.subjectin vitro study
dc.subjectMTT assay
dc.subjectnanoencapsulation
dc.subjectparticle size
dc.subjectphysical chemistry
dc.subjectpriority journal
dc.subjectquantitative analysis
dc.subjectumbilical vein endothelial cell
dc.subjectzeta potential
dc.titleMarrubiin-loaded solid lipid nanoparticles' impact on TNF-? treated umbilical vein endothelial cells: A study for cardioprotective effect
dc.typeArticle
dc.citation.volume164
dc.citation.spage299
dc.citation.epage307
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1016/j.colsurfb.2018.01.046


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