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Artificial vascularized scaffolds for 3D-tissue regeneration — a report of the ArtiVasc 3D Project

            order to integrate with the newly developed combined    technologies in one process,
            AM  process,  computer  programs  were  devised  that   •   To build a test rig where the combination of the
            sliced the CAD model and produced appropriate layer     technologies  can  be examined  and  developed
            data for each aspect of the AM process. This included   further.
            image data to drive the inkjet printing steps and vector
            files to control the stereolithography steps.
               For the AM process development, the first task was
            to test the new materials for their suitability for inkjet
            printing and to define the optimal printing parameters.
            Secondly, MPP was adapted with regard to the devel-
            oped  material  and the desired scaffold structures  by
            developing  appropriate beam  guidance and optics.
            Thirdly, the materials were tested for their suitability
            in the electrospinning process  and to define the
            process parameters. Further work involved the devel-
            opment of a process-strategy and concept for combin-
            ing inkjet, MPP and electrospinning and then to ex-  Figure 2.  The user interface for the automated generation of
            amine the co-action of all three production technolo-  vessel designs.

            gies. This required a test rig including all three tech-
            nologies to be produced, as well as the development   5.3 Objectives of WP7
            and generation of the necessary machine control code   The overall goal was to develop the integrated mach-
            enabling process-integration and optimization.     ine prototype encompassing the developed processes
            5.1 Objectives of WP3                              through a set of pre- and post-processing steps. Spec-
                                                               ific objectives were:
            The overall goal was the  modelling and design of a   •   To establish the  machine  prototype specifica-
            vascular system that effectively delivers O 2 and other   tions for the machine demonstrator,
            nutrients from the circulating blood flow to the sur-  •   To develop prototype solutions for the produc-
            rounding tissue. Specific objectives were:              tion  module,  combining  inkjet  printing,  MPP
              •   To  investigate the nutrient permeation  within   and electrospinning and modules for necessary
                  the vascular system to the cells,                 pre- and post-processing steps,
              •   To identify the requirements for the blood flow   •   To  manufacture  and implement the integrated
                  through  the  system  and  provide  an  informed   machine prototype,
                  design specification,                          •   To  set the prototype into  service, commissio-
              •   To develop design tools for generating 3D CAD     ning, parameters tuning and equipment adjust-
                  models of optimum vascular systems (see Fig-      ment.
                  ure 2) [11,12] ,                             5.4 Objectives of WP8
              •   To translate 3D models into an appropriate data
                  format for the proposed AM process.          The overall goal was to demonstrate and test the pro-
                                                               totype process and equipment resulting from WP7.
            5.2 Objectives of WP4                              Specific objectives were:
            The overall goal was to develop  a  combined  AM     •   To demonstrate the fulfilment of requirements
            process that integrates inkjet printing, MPP and elec-  for the scaffold generation,
            trospinning to  work as one single process. Specific   •   To make fully functional scaffolds for analysis,
            objectives were:                                     •   To produce scaffolds for biological applications.
              •   To deliver machine specification for building a   5.5 Highlights
                  working process module in WP7,
              •   To  iteratively  adapt and  optimize the process   The three AM processes have been installed and ex-
                  for each process technology in cooperation with   tensively characterized. By using UV-curing it could be
                  material development,                        demonstrated that vessels with different geometries and
              •   To develop a strategy for combining these three   sizes could be generated  either by MPP with dimen-

            96                          International Journal of Bioprinting (2016)–Volume 2, Issue 1
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