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Melt electrospinning of poly(ε-caprolactone) scaffolds: phenomenological observations associated with collection and direct writing.
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för kirurgiska vetenskaper, Öron-, näs- och halssjukdomar.
Vise andre og tillknytning
2014 (engelsk)Inngår i: Materials science & engineering. C, biomimetic materials, sensors and systems, ISSN 0928-4931, E-ISSN 1873-0191, Vol. 45Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Melt electrospinning and its additive manufacturing analogue, melt electrospinning writing (MEW), are two processes which can produce porous materials for applications where solvent toxicity and accumulation in solution electrospinning are problematic. This study explores the melt electrospinning of poly(ε-caprolactone) (PCL) scaffolds, specifically for applications in tissue engineering. The research described here aims to inform researchers interested in melt electrospinning about technical aspects of the process. This includes rapid fiber characterization using glass microscope slides, allowing influential processing parameters on fiber morphology to be assessed, as well as observed fiber collection phenomena on different collector substrates. The distribution and alignment of melt electrospun PCL fibers can be controlled to a certain degree using patterned collectors to create large numbers of scaffolds with shaped macroporous architectures. However, the buildup of residual charge in the collected fibers limits the achievable thickness of the porous template through such scaffolds. One challenge identified for MEW is the ability to control charge buildup so that fibers can be placed accurately in close proximity, and in many centimeter heights. The scale and size of scaffolds produced using MEW, however, indicate that this emerging process will fill a technological niche in biofabrication.

sted, utgiver, år, opplag, sider
2014. Vol. 45
Emneord [en]
Blood coagulation, endothelial cells, heparin, surface modification, collagen
HSV kategori
Identifikatorer
URN: urn:nbn:se:uu:diva-266582DOI: 10.1016/j.msec.2014.07.034PubMedID: 25491879OAI: oai:DiVA.org:uu-266582DiVA, id: diva2:868334
Tilgjengelig fra: 2015-11-10 Laget: 2015-11-10 Sist oppdatert: 2017-12-01

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