Layla Bashir Larsen

Fabrication of scalable and structured tissue engineering scaffolds using water dissolvable sacrificial 3D printed moulds.

One of the major challenges in producing large scale engineered tissue is the lack of ability to create large highly perfused scaffolds in which cells can grow at a high cell density and viability. Here, we explore 3D printed polyvinyl alcohol (PVA) as a sacrificial mould in a polymer casting process. The PVA mould network defines the channels and is dissolved after curing the polymer casted around it. The printing parameters determined the PVA filament density in the sacrificial structure and this density resulted in different stiffness of the corresponding elastomer replica. It was possible to achieve 80% porosity corresponding to about 150 cm(2)/cm(3) surface to volume ratio. The process is easily scalable as demonstrated by fabricating a 75 cm(3) scaffold with about 16,000 interconnected channels (about 1m(2) surface area) and with a channel to channel distance of only 78 μm. To our knowledge this is the largest scaffold ever to be produced with such small feature sizes and with so many structured channels. The fabricated scaffolds were applied for in-vitro culturing of hepatocytes over a 12-day culture period. Smaller scaffolds (6×4 mm) were tested for cell culturing and could support homogeneous cell growth throughout the scaffold. Presumably, the diffusion of oxygen and nutrient throughout the channel network is rapid enough to support cell growth. In conclusion, the described process is scalable, compatible with cell culture, rapid, and inexpensive.

Differentiation of human-induced pluripotent stem cell under flow conditions to mature hepatocytes for liver tissue engineering

Hepatic differentiation of human‐induced pluripotent stem cells (hiPSCs) under flow conditions in a 3D scaffold is expected to be a major step forward for construction of bioartificial livers. The aims of this study were to induce hepatic differentiation of hiPSCs under perfusion conditions and to perform functional comparisons with fresh human precision‐cut liver slices (hPCLS), an excellent benchmark for the human liver in vivo. The majority of the mRNA expression of CYP isoenzymes and transporters and the tested CYP activities, Phase II metabolism, and albumin, urea, and bile acid synthesis in the hiPSC‐derived cells reached values that overlap those of hPCLS, which indicates a higher degree of hepatic differentiation than observed until now. Differentiation under flow compared with static conditions had a strong inducing effect on Phase II metabolism and suppressed AFP expression but resulted in slightly lower activity of some of the Phase I metabolism enzymes. Gene expression data indicate that hiPSCs differentiated into both hepatic and biliary directions. In conclusion, the hiPSC differentiated under flow conditions towards hepatocytes express a wide spectrum of liver functions at levels comparable with hPCLS indicating excellent future perspectives for the development of a bioartificial liver system for toxicity testing or as liver support device for patients.

Electrical impedance tomography methods for miniaturised 3D systems

Abstract In this study, we explore the potential of electrical impedance tomography (EIT) for miniaturised 3D samples to provide a non-invasive approach for future applications in tissue engineering and 3D cell culturing. We evaluated two different electrode configurations using an array of nine circular chambers (Ø 10 mm), each having eight gold plated needle electrodes vertically integrated along the chamber perimeter. As first method, the adjacent electrode configuration was tested solving the computationally simple back-projection algorithm using Comsol Multiphysics in time-difference EIT (t-EIT). Subsequently, a more elaborate method based on the “polar-offset” configuration (having an additional electrode at the centre of the chamber) was evaluated using linear t-EIT and linear weighted frequency-difference EIT (f-EIT). Image reconstruction was done using a customised algorithm that has been previously validated for EIT imaging of neural activity. All the finite element simulations and impedance measurements on test objects leading to image reconstruction utilised an electrolyte having an ionic strength close to physiological solutions. The chosen number of electrodes and consequently number of electrode configurations aimed at maximising the quality of image reconstruction while minimising the number of required measurements. This is significant when designing a technique suitable for tissue engineering applications where time-based monitoring of cellular behaviour in 3D scaffolds is of interest. The performed tests indicated that the method based on the adjacent configuration in combination with the back-projection algorithm was only able to provide image reconstruction when using a test object having a higher conductivity than the background electrolyte. Due to limitations in the mesh quality, the reconstructed image had significant irregularities and the position was slightly shifted toward the perimeter of the chamber. On the other hand, the method based on the polar-offset configuration combined with the customised algorithm proved to be suitable for image reconstruction when using non-conductive and cell-based test objects (down to 1% of the measurement chamber volume), indicating its suitability for future tissue engineering applications with polymeric scaffolds.