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contributor authorXinsheng Gao
contributor authorBrian P. Grady
contributor authorKenneth J. Dormer
contributor authorRichard D. Kopke
contributor authorYoudan Wang
contributor authorKejian Chen
date accessioned2017-05-09T00:40:14Z
date available2017-05-09T00:40:14Z
date copyrightAugust, 2010
date issued2010
identifier issn1949-2944
identifier otherJNEMAA-28038#031010_1.pdf
identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/144535
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.
publisherThe American Society of Mechanical Engineers (ASME)
titleMagnetic Assisted Transport of PLGA Nanoparticles Through a Human Round Window Membrane Model
typeJournal Paper
journal volume1
journal issue3
journal titleJournal of Nanotechnology in Engineering and Medicine
identifier doi10.1115/1.4002043
journal fristpage31010
identifier eissn1949-2952
keywordsMagnetic fields
keywordsNanoparticles
keywordsParticulate matter
keywordsMembranes
keywordsPLGA
keywordsHydrogels
keywordsWater
keywordsDrug delivery systems
keywordsMagnets
keywordsEar
keywordsDensity AND Iron
treeJournal of Nanotechnology in Engineering and Medicine:;2010:;volume( 001 ):;issue: 003
contenttypeFulltext


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