Publication:
Formulation development and in vitro evaluation of transferrin-conjugated liposomes as a carrier of ganciclovir targeting the retina

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.date.issuedBE2563
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.format.mimetypeapplication/pdf
dc.identifier.citationInternational Journal of Pharmaceutics. Vol 577, (2020)
dc.identifier.doi10.1016/j.ijpharm.2020.119084
dc.identifier.issn3785173
dc.identifier.other2-s2.0-85078451640
dc.identifier.urihttps://swu-dspace2.eval.plus/handle/123456789/4626
dc.rights.holderมหาวิทยาลัยศรีนครินทรวิโรฒ
dc.subject.otherDrug carrier
dc.subject.otherGanciclovir
dc.subject.otherGlycoprotein B
dc.subject.otherLiposome
dc.subject.otherTransferrin
dc.subject.otherAntivirus agent
dc.subject.otherDrug carrier
dc.subject.otherGanciclovir
dc.subject.otherLiposome
dc.subject.otherTransferrin
dc.subject.otherAntiviral activity
dc.subject.otherARPE-19 cell line
dc.subject.otherArticle
dc.subject.otherCell surface
dc.subject.otherControlled study
dc.subject.otherCytotoxicity test
dc.subject.otherDispersity
dc.subject.otherDrug conjugation
dc.subject.otherDrug delivery system
dc.subject.otherDrug formulation
dc.subject.otherDrug release
dc.subject.otherEndocytosis
dc.subject.otherEndosome
dc.subject.otherFourier transform infrared spectroscopy
dc.subject.otherHuman
dc.subject.otherHuman cell
dc.subject.otherIn vitro study
dc.subject.otherInternalization
dc.subject.otherParticle size
dc.subject.otherPhysical chemistry
dc.subject.otherPriority journal
dc.subject.otherRetina cell
dc.subject.otherRetinal pigment epithelium
dc.subject.otherZeta potential
dc.subject.otherCell line
dc.subject.otherChemistry
dc.subject.otherComparative study
dc.subject.otherCytology
dc.subject.otherCytomegalovirus retinitis
dc.subject.otherIntravitreal drug administration
dc.subject.otherMetabolism
dc.subject.otherTopical drug administration
dc.subject.otherAdministration, Topical
dc.subject.otherAntiviral Agents
dc.subject.otherCell Line
dc.subject.otherCytomegalovirus Retinitis
dc.subject.otherDrug Carriers
dc.subject.otherDrug Delivery Systems
dc.subject.otherGanciclovir
dc.subject.otherHumans
dc.subject.otherIntravitreal Injections
dc.subject.otherLiposomes
dc.subject.otherParticle Size
dc.subject.otherRetinal Pigment Epithelium
dc.subject.otherTransferrin
dc.titleFormulation development and in vitro evaluation of transferrin-conjugated liposomes as a carrier of ganciclovir targeting the retina
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85078451640&doi=10.1016%2fj.ijpharm.2020.119084&partnerID=40&md5=a6fc280a6249dfb9d2fed6fbda55d966

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