Show simple item record

dc.contributor.authorXinsheng Gao
dc.contributor.authorBrian P. Grady
dc.contributor.authorKenneth J. Dormer
dc.contributor.authorRichard D. Kopke
dc.contributor.authorYoudan Wang
dc.contributor.authorKejian Chen
dc.date.accessioned2017-05-09T00:40:14Z
dc.date.available2017-05-09T00:40:14Z
dc.date.copyrightAugust, 2010
dc.date.issued2010
dc.identifier.issn1949-2944
dc.identifier.otherJNEMAA-28038#031010_1.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl/handle/yetl/144535
dc.description.abstractThe lack of an effective method for inner ear drug delivery is a clinical problem for the prevention and treatment of hearing loss. With technology advances in nanomedicine and the use of hydrogels, more drug delivery options are becoming available. This study tested the feasibility of using a tripartite layer round window membrane (RWM) model to evaluate the effectiveness of a magnetic assisted transport of poly(lactic-co-glycolic acid) (PLGA)/superparamagnetic iron oxide nanoparticles (SPIONs). A RWM model was constructed as a three-cell-layer model with epithelial cells cultured on both sides of a small intestinal submucosal (SIS) matrix with fibroblasts seeded within the matrix. PLGA encapsulated coumarin-6/SPION nanoparticles 100 nm in diameter were formulated by an oil-in-water emulsion/solvent evaporation method and pulled through the RWM model using permanent magnets with a flux density 0.410 T at the pole face. Independent variables such as external magnetic force and exposure time, composition of hyaluronic acid (HA) hydrogel suspending media, and particle characteristics including magnetic susceptibility were studied. Magnetic assisted transport of coumarin-6 labeled magnetic nanoparticles through the RWM inserts increased 2.1-fold in 1 h compared with the controls. HA hydrogel did prevent particle accumulation on the surface of RWM in a magnetic field but also impaired the mobility of these particles. Greater particle susceptibility or stronger external magnetic fields did not significantly improve the transmembrane transport. A RWM model was designed consisting of a SIS membrane and three co-cultured layers of cells, which was structurally and physically similar to the human. PLGA particles (100 nm) with encapsulated ∼15 nm SPIONs were transported through this model with the assistance of an external magnet, allowing quantitative evaluation of prospective targeted drug delivery through the RWM via the assistance of a magnetic field.
dc.publisherThe American Society of Mechanical Engineers (ASME)
dc.titleMagnetic Assisted Transport of PLGA Nanoparticles Through a Human Round Window Membrane Model
dc.typeJournal Paper
dc.journal.volume1
dc.journal.issue3
dc.journal.titleJournal of Nanotechnology in Engineering and Medicine
dc.identifier.doi10.1115/1.4002043
dc.journal.fristpage31010
dc.identifier.eissn1949-2952
dc.keywordsMagnetic fields
dc.keywordsNanoparticles
dc.keywordsParticulate matter
dc.keywordsMembranes
dc.keywordsPLGA
dc.keywordsHydrogels
dc.keywordsWater
dc.keywordsDrug delivery systems
dc.keywordsMagnets
dc.keywordsEar
dc.keywordsDensity AND Iron
dc.treeJournal of Nanotechnology in Engineering and Medicine:;2010:;volume( 001 ):;issue: 003
dc.contenttypeFulltext


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record