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Tekijä: | Korpela, Jyrki |
Työn nimi: | Fused deposition modeling of biodegradable polymeric scaffolds |
Biohajoavien polymeeristen kudosteknologian tukirakenteiden 3D-pikavalmistus pursotusmenetelmällä | |
Julkaisutyyppi: | Diplomityö |
Julkaisuvuosi: | 2012 |
Sivut: | [8] + 100 s. + liitt. 24 Kieli: eng |
Koulu/Laitos/Osasto: | Sähkötekniikan korkeakoulu |
Oppiaine: | Polymeeriteknologia (Kem-100) |
Valvoja: | Seppälä, Jukka |
Ohjaaja: | Korhonen, Harri ; Malin, Minna |
OEVS: | Sähköinen arkistokappale on luettavissa Aalto Thesis Databasen kautta.
Ohje Digitaalisten opinnäytteiden lukeminen Aalto-yliopiston Harald Herlin -oppimiskeskuksen suljetussa verkossaOppimiskeskuksen suljetussa verkossa voi lukea sellaisia digitaalisia ja digitoituja opinnäytteitä, joille ei ole saatu julkaisulupaa avoimessa verkossa. Oppimiskeskuksen yhteystiedot ja aukioloajat: https://learningcentre.aalto.fi/fi/harald-herlin-oppimiskeskus/ Opinnäytteitä voi lukea Oppimiskeskuksen asiakaskoneilla, joita löytyy kaikista kerroksista.
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Sijainti: | P1 Ark Aalto 898 | Arkisto |
Avainsanat: | fused deposition modeling tissue engineering scaffolds trachea scaffolds 3D-pikavalmistus pursotus kudosteknologian tukirakenteet trakean tukirakenteet |
Tiivistelmä (eng): | Three-dimensional printing (3DP) consists of a group of promising additive manufacturing techniques which can be utilized in tissue engineering applications. Fused deposition modelling (FDM) is a less studied 3DP method capable of utilizing thermoplastic common biopolymers. Little attention has been previously paid to examining the suitability of this method to such applications. The purpose of this thesis was to determine the feasibility of FDM to tissue engineering scaffold design and manufacturing. The feasibility was investigated by examining the potential material scope, the mechanical properties of FDM-printed porous structures, and the cell-cultural response to the structures by studying the proliferation on the scaffold surface. This study demonstrated the printability of a poly (epsilon-caprolactone) bioactive glass (PCL/BAG) composite as well as L-lactide/epsilon-caprolactone 75/25 mol-% copolymers for the first time as far as we know. SEM images showed BAG particles at the surface of the printed PCL/BAG scaffolds. The mechanical testing showed the possibility to alter the compressive stiffness of a scaffold matrix without a change in the compressive modulus. A structure with 0°/90° raster angles and vertical pore channels was vertically approximately 60-% stiffer than the structure with 0°/90° raster angles and diagonal pore channels. A structure with 0°/60°/120° raster angles was as stiff vertically compared to the first matrix but horizontally 25-% to 50-% less stiff. The horizontal compressive modules were 12-% to 39-% higher than vertical compressive modules, suggesting strong adhesion between the layers. The proliferation results suggested polylactide (PLA) is superior material over PCL or PCL/BAG -composite for cell growth. The proliferation was three times higher in PLA than in other materials. Bioactive glass evoked no significant additional cell growth compared to pure PCL structures. Light microscope and SEM images showed both the viability and the oriented structure of the cells. The cells were growing in multiple layers, and the biocompatibility of the structures was demonstrated. Finally, a model trachea scaffold with interconnected pores and 40 % porosity was created to show the applicability of FDM for porous scaffold design. |
ED: | 2012-09-24 |
INSSI tietueen numero: 45287
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