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contributor authorSaif Khalil
contributor authorWei Sun
date accessioned2017-05-09T00:31:28Z
date available2017-05-09T00:31:28Z
date copyrightNovember, 2009
date issued2009
identifier issn0148-0731
identifier otherJBENDY-27068#111002_1.pdf
identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/139816
description abstractAdvanced solid freeform fabrication (SFF) techniques have been an interest for constructing tissue engineered polymeric scaffolds because of its repeatability and capability of high accuracy in fabrication resolution at the scaffold macro- and microscales. Among many important scaffold applications, hydrogel scaffolds have been utilized in tissue engineering as a technique to confide the desired proliferation of seeded cells in vitro and in vivo into its architecturally porous three-dimensional structures. Such fabrication techniques not only enable the reconstruction of scaffolds with accurate anatomical architectures but also enable the ability to incorporate bioactive species such as growth factors, proteins, and living cells. This paper presents a bioprinting system designed for the freeform fabrication of porous alginate scaffolds with encapsulated endothelial cells. The bioprinting fabrication system includes a multinozzle deposition system that utilizes SFF techniques and a computer-aided modeling system capable of creating heterogeneous tissue scaffolds. The manufacturing process is biologically compatible and is capable of functioning at room temperature and relatively low pressures to reduce the fluidic shear forces that could deteriorate biologically active species. The deposition system resolution is 10 μm in the three orthogonal directions XYZ and has minimum velocity of 100 μm/s. The ideal concentrations of sodium alginate and calcium chloride were investigated to determine a viable bioprinting process. The results indicated that the suitable fabrication parameters were 1.5% (w/v) sodium alginate and 0.5% (w/v) calcium chloride. Degradation studies via mechanical testing showed a decrease in the elastic modulus by 35% after 3 weeks. Cell viability studies were conducted on the cell encapsulated scaffolds for validating the bioprinting process and determining cell viability of 83%. This work exhibits the potential use of accurate cell placement for engineering complex tissue regeneration using computer-aided design systems.
publisherThe American Society of Mechanical Engineers (ASME)
titleBioprinting Endothelial Cells With Alginate for 3D Tissue Constructs
typeJournal Paper
journal volume131
journal issue11
journal titleJournal of Biomechanical Engineering
identifier doi10.1115/1.3128729
journal fristpage111002
identifier eissn1528-8951
keywordsManufacturing
keywordsStress
keywordsShear (Mechanics)
keywordsBiological tissues
keywordsDisks
keywordsSodium
keywordsTissue engineering
keywordsTissue scaffolds
keywordsEndothelial cells
keywordsOptimization
keywordsElastic moduli
keywordsDesign
keywordsHydrogels
keywordsDensity
keywordsComputer-aided design
keywordsForce AND Biological cells
treeJournal of Biomechanical Engineering:;2009:;volume( 131 ):;issue: 011
contenttypeFulltext


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