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contributor authorRiffard Jean-Gilles
contributor authorDavid Soscia
contributor authorSharon Sequeira
contributor authorMichael Melfi
contributor authorAnand Gadre
contributor authorJames Castracane
contributor authorMelinda Larsen
date accessioned2017-05-09T00:40:14Z
date available2017-05-09T00:40:14Z
date copyrightAugust, 2010
date issued2010
identifier issn1949-2944
identifier otherJNEMAA-28038#031008_1.pdf
identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/144532
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.
publisherThe American Society of Mechanical Engineers (ASME)
titleNovel Modeling Approach to Generate a Polymeric Nanofiber Scaffold for Salivary Gland Cells
typeJournal Paper
journal volume1
journal issue3
journal titleJournal of Nanotechnology in Engineering and Medicine
identifier doi10.1115/1.4001744
journal fristpage31008
identifier eissn1949-2952
keywordsFibers
keywordsTransfer functions
keywordsElectrospinning
keywordsNanofibers
keywordsTissue scaffolds
keywordsPLGA
keywordsModeling
keywordsBiological tissues
keywordsGlass
keywordsDesign
keywordsneedles AND Self-organization
treeJournal of Nanotechnology in Engineering and Medicine:;2010:;volume( 001 ):;issue: 003
contenttypeFulltext


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