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Optimized vascular network by stereolithography for tissue engineered skin












































           Figure 13. Results of the WST-1 assays. The Box-whisker-plots indicate the median in the centre of the box, 25th and 75th percentile by
           the lower and upper margin of the box, 10th and 90th percentile by the whiskers and values outside this range.





           4.3  Degradation test of a printed tube             4.4   In vitro testing

           The gravimetric analysis of the dip-coated tubes shows a   hASCs were evaluated regarding their viability using a
           slight mass loss of approximately -1% (-1.9%) after two   live/dead assay for seven days of culture. Results of cell
           months shaking in PBS buffer (H O  respectively) with   viability are shown in Figure 17. Figure 17 illustrates the
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           a standard deviation of 0.5% (1.9%). The results of the   cell vitality within a 1 x 1 cm hydrogel supported via a
           tubes show no uniform degradation behaviour, which   stainless steel moulded central tube (Figure 17(A)), an
           would have to be expressed in a mass decrease. In some   SLA-formed branched PA tube containing pores (Figure
           measurements, even mass increases were observed,    17(B–C)) and a single central SLA-formed PA tube
           which could probably be due to inclusions of PBS    containing pores (Figure 17(D)). By comparing Figure
           salts. Overall, it is assumed that the inconsistent results   17(A,B), it is demonstrated that the ability of a branched
           in the stereolithographic samples are due to a non-  tube can support the whole volume more appropriately
           homogeneous production method and the results show   compared with the central steel tube. Additionally, it
           no significant degradation effect rather than the washing   is also shown that the surrounding cells get in contact
           out of not reacted monomers and inclusion effects   to parts of the material, infiltrating the pores (in Figure
           since we could not observe structural changes of the   17(C)) and form more complex structures within the
           samples by sight test. The more uniform results with less   hydrogel (in Figure 17(D)).
           scattering of the dip-coated samples show, although very   Figure 18 gives a preliminary comparison of dead cell
           low mass loss both in the hydrolytic and oxidative cases.   rate with different embedded tubes. It can be seen from
           So we can assume a very slow degradable material.   this picture that after seven days, cell death rate in the


           12                          International Journal of Bioprinting (2018)–Volume 4, Issue 2
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