Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/11978
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dc.contributor.authorAsasutjarit R.
dc.contributor.authorManagit C.
dc.contributor.authorPhanaksri T.
dc.contributor.authorTreesuppharat W.
dc.contributor.authorFuongfuchat A.
dc.date.accessioned2021-04-05T03:01:34Z-
dc.date.available2021-04-05T03:01:34Z-
dc.date.issued2020
dc.identifier.issn3785173
dc.identifier.other2-s2.0-85078451640
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/11978-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85078451640&doi=10.1016%2fj.ijpharm.2020.119084&partnerID=40&md5=a6fc280a6249dfb9d2fed6fbda55d966
dc.description.abstractGanciclovir (GCV) is an antiviral drug approved for treatment of cytomegalovirus (CMV) retinitis. It can be delivered to the eye via systemic administrations. However, local delivery of GCV that targets the retina is considered as an alternative to increase efficacy of the treatment and lessen side effects. Thus, this study aimed to develop formulations of transferrin (Tf)-conjugated liposomes containing GCV (Tf-GCV-LPs) for intravitreal injection and topical instillation. Tf-GCV-LPs were prepared by the reverse-phase evaporation technique and then conjugated to Tf. Their physicochemical properties were evaluated. The optimized formulation was selected and subjected to the cytotoxicity test, cellular uptake study in the human retinal pigment epithelial cells (the ARPE-19 cells) and antiviral activity evaluation. The results showed that physicochemical properties of Tf-GCV-LPs were affected by formulation compositions. The optimized Tf-GCV-LPs had a particle size lower than 100 nm with a negative value of zeta potential. They were safe for the ARPE-19 cells. These Tf-GCV-LPs were taken up by these cells via Tf receptors-mediated endocytosis and showed inhibitory activity on CMV in the infected cells. Therefore, the optimized Tf-GCV-LPs could be accepted as a promising drug delivery system for targeted GCV delivery to the retina in the treatment of CMV retinitis. © 2020 Elsevier B.V.
dc.subjectdrug carrier
dc.subjectganciclovir
dc.subjectglycoprotein B
dc.subjectliposome
dc.subjecttransferrin
dc.subjectantivirus agent
dc.subjectdrug carrier
dc.subjectganciclovir
dc.subjectliposome
dc.subjecttransferrin
dc.subjectantiviral activity
dc.subjectARPE-19 cell line
dc.subjectArticle
dc.subjectcell surface
dc.subjectcontrolled study
dc.subjectcytotoxicity test
dc.subjectdispersity
dc.subjectdrug conjugation
dc.subjectdrug delivery system
dc.subjectdrug formulation
dc.subjectdrug release
dc.subjectendocytosis
dc.subjectendosome
dc.subjectFourier transform infrared spectroscopy
dc.subjecthuman
dc.subjecthuman cell
dc.subjectin vitro study
dc.subjectinternalization
dc.subjectparticle size
dc.subjectphysical chemistry
dc.subjectpriority journal
dc.subjectretina cell
dc.subjectretinal pigment epithelium
dc.subjectzeta potential
dc.subjectcell line
dc.subjectchemistry
dc.subjectcomparative study
dc.subjectcytology
dc.subjectCytomegalovirus retinitis
dc.subjectintravitreal drug administration
dc.subjectmetabolism
dc.subjecttopical drug administration
dc.subjectAdministration, Topical
dc.subjectAntiviral Agents
dc.subjectCell Line
dc.subjectCytomegalovirus Retinitis
dc.subjectDrug Carriers
dc.subjectDrug Delivery Systems
dc.subjectGanciclovir
dc.subjectHumans
dc.subjectIntravitreal Injections
dc.subjectLiposomes
dc.subjectParticle Size
dc.subjectRetinal Pigment Epithelium
dc.subjectTransferrin
dc.titleFormulation development and in vitro evaluation of transferrin-conjugated liposomes as a carrier of ganciclovir targeting the retina
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationInternational Journal of Pharmaceutics. Vol 577, (2020)
dc.identifier.doi10.1016/j.ijpharm.2020.119084
Appears in Collections:Scopus 1983-2021

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