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dc.contributor.authorRiffard Jean-Gilles
dc.contributor.authorDavid Soscia
dc.contributor.authorSharon Sequeira
dc.contributor.authorMichael Melfi
dc.contributor.authorAnand Gadre
dc.contributor.authorJames Castracane
dc.contributor.authorMelinda Larsen
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#031008_1.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl/handle/yetl/144532
dc.description.abstractElectrospun nanofibers have been utilized in many biomedical applications as biomimetics of extracellular matrix proteins that promote self-organization of cells into 3D tissue constructs. As progress toward an artificial salivary gland tissue construct, we prepared nanofiber scaffolds using PLGA, which is a biodegradable and biocompatible material. We used electrospinning to prepare nanofiber scaffolds using poly(lactic-co-glycolic acid) (PLGA) with both dimethylformamide (DMF) and hexafluoroisopropanol (HFIP) as solvents. Using a design of experiment approach, the system and process parameters were optimized concurrently, and their effects on the diameter of the resulting fibers were computed into a single model. A transfer function was used to reproducibly produce nanofibers of a defined diameter, which was confirmed by a scanning electron microscope. The salivary gland cell line was seeded on the nanofiber scaffolds, and morphology, cell proliferation, and viability were assayed. Varying two or more parameters simultaneously yielded trends diverging from the linear response predicted by previous studies. Comparison of two solvents revealed that the diameter of PLGA nanofibers generated using HFIP is less sensitive to changes in the system and process parameters than are fibers generated using DMF. Inclusion of NaCl reduced morphological inconsistencies and minimized process variability. The resulting nanofiber scaffolds supported attachment, survival, and cell proliferation of a mouse salivary gland epithelial cell line. In comparison with glass and flat PLGA films, the nanofibers promoted self-organization of the salivary gland cells into 3D cell clusters, or aggregates. These data indicate that nanofiber scaffolds promote salivary gland cell organization, and suggest that a nanofiber scaffold could provide a platform for engineering of an artificial salivary gland tissue construct. This study additionally provides a method for efficient production of nanofiber scaffolds for general application in tissue engineering.
dc.publisherThe American Society of Mechanical Engineers (ASME)
dc.titleNovel Modeling Approach to Generate a Polymeric Nanofiber Scaffold for Salivary Gland Cells
dc.typeJournal Paper
dc.journal.volume1
dc.journal.issue3
dc.journal.titleJournal of Nanotechnology in Engineering and Medicine
dc.identifier.doi10.1115/1.4001744
dc.journal.fristpage31008
dc.identifier.eissn1949-2952
dc.keywordsFibers
dc.keywordsTransfer functions
dc.keywordsElectrospinning
dc.keywordsNanofibers
dc.keywordsTissue scaffolds
dc.keywordsPLGA
dc.keywordsModeling
dc.keywordsBiological tissues
dc.keywordsGlass
dc.keywordsDesign
dc.keywordsneedles AND Self-organization
dc.treeJournal of Nanotechnology in Engineering and Medicine:;2010:;volume( 001 ):;issue: 003
dc.contenttypeFulltext


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