2017
DOI: 10.1016/j.biomaterials.2016.10.040
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Electrospinning versus microfluidic spinning of functional fibers for biomedical applications

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Cited by 295 publications
(246 citation statements)
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“…Current methods of preparing fibers mainly include melt spinning,14 wet spinning,15,16 and electrospinning 17–19. However, the presence of high temperatures and volatile solvents in the melt spinning and electrospinning processes limits the encapsulation of cells, microtissues, and other bioactive molecules in fibers 20. For example, electrospinning microfibers must be removed with organic solvents before they can be used as a substrate for cell culture, which limits the construction of more complex 3D tissues.…”
Section: Introductionmentioning
confidence: 99%
“…Current methods of preparing fibers mainly include melt spinning,14 wet spinning,15,16 and electrospinning 17–19. However, the presence of high temperatures and volatile solvents in the melt spinning and electrospinning processes limits the encapsulation of cells, microtissues, and other bioactive molecules in fibers 20. For example, electrospinning microfibers must be removed with organic solvents before they can be used as a substrate for cell culture, which limits the construction of more complex 3D tissues.…”
Section: Introductionmentioning
confidence: 99%
“…[ 16,17,19,20 ] The first commonly used approach is the electrospinning technique that has been intensively applied due to the advantages of reproducibility, simplicity, and diversity in producing fibers with micro‐ or nanoscale diameters and different topographical features. [ 21,22 ] The fibers' membrane produced by electrospinning can provide large surface areas for cells to attach and proliferate, which could also enhance the penetration of nutrients and oxygen. [ 23,24 ] However, electrospinning is hard to fabricate 3D structure due to the nanoscale of fibers, which results in 2D structures in most cases.…”
Section: Introductionmentioning
confidence: 99%
“…(MS2b) Localization of encapsulated cells in the outer layer of the DEM-MA matrix-core/shell capsule (cells nuclei: blue-4′,6-diamidine-2′-phenylindole dihydrochloride (DAPI); F-actin filaments: red-phalloidin). [64,[67][68][69][70][71][72][73][74][75][76] Microfibers are continuously formed in a microchannel with a coaxial flow composed by the fiber precursor solution and sheathed by the crosslinking agent. Adapted with permission.…”
Section: Fiber-shaped Systemsmentioning
confidence: 99%