Novel Modeling Approach to Generate a Polymeric Nanofiber Scaffold for Salivary Gland CellsSource: Journal of Nanotechnology in Engineering and Medicine:;2010:;volume( 001 ):;issue: 003::page 31008Author:Riffard Jean-Gilles
,
David Soscia
,
Sharon Sequeira
,
Michael Melfi
,
Anand Gadre
,
James Castracane
,
Melinda Larsen
DOI: 10.1115/1.4001744Publisher: The American Society of Mechanical Engineers (ASME)
Abstract: Electrospun 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.
keyword(s): Fibers , Transfer functions , Electrospinning , Nanofibers , Tissue scaffolds , PLGA , Modeling , Biological tissues , Glass , Design , needles AND Self-organization ,
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contributor author | Riffard Jean-Gilles | |
contributor author | David Soscia | |
contributor author | Sharon Sequeira | |
contributor author | Michael Melfi | |
contributor author | Anand Gadre | |
contributor author | James Castracane | |
contributor author | Melinda Larsen | |
date accessioned | 2017-05-09T00:40:14Z | |
date available | 2017-05-09T00:40:14Z | |
date copyright | August, 2010 | |
date issued | 2010 | |
identifier issn | 1949-2944 | |
identifier other | JNEMAA-28038#031008_1.pdf | |
identifier uri | http://yetl.yabesh.ir/yetl/handle/yetl/144532 | |
description abstract | Electrospun 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. | |
publisher | The American Society of Mechanical Engineers (ASME) | |
title | Novel Modeling Approach to Generate a Polymeric Nanofiber Scaffold for Salivary Gland Cells | |
type | Journal Paper | |
journal volume | 1 | |
journal issue | 3 | |
journal title | Journal of Nanotechnology in Engineering and Medicine | |
identifier doi | 10.1115/1.4001744 | |
journal fristpage | 31008 | |
identifier eissn | 1949-2952 | |
keywords | Fibers | |
keywords | Transfer functions | |
keywords | Electrospinning | |
keywords | Nanofibers | |
keywords | Tissue scaffolds | |
keywords | PLGA | |
keywords | Modeling | |
keywords | Biological tissues | |
keywords | Glass | |
keywords | Design | |
keywords | needles AND Self-organization | |
tree | Journal of Nanotechnology in Engineering and Medicine:;2010:;volume( 001 ):;issue: 003 | |
contenttype | Fulltext |