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@PHDTHESIS{Hansen:1020439,
      author       = {Hansen, Nadja},
      othercontributors = {Fischer, Horst and Jockenhövel, Stefan},
      title        = {{E}ntwicklung eines 3{D}-biogedruckten
                      {B}lutgefäßersatzes zur {U}ntersuchung des zellulären
                      {V}erhaltens in {I}n-vitro-{G}ewebemodellen unter
                      dynamischer {K}ultivierung},
      school       = {Rheinisch-Westfälische Technische Hochschule Aachen},
      type         = {Dissertation},
      address      = {Aachen},
      publisher    = {RWTH Aachen University},
      reportid     = {RWTH-2025-08995},
      pages        = {1 Online-Ressource : Illustrationen},
      year         = {2025},
      note         = {Veröffentlicht auf dem Publikationsserver der RWTH Aachen
                      University 2026; Dissertation, Rheinisch-Westfälische
                      Technische Hochschule Aachen, 2025},
      abstract     = {The present work describes the development of a novel
                      3D-bioprinted in vitro model of a blood vessel to provide
                      new insights into the mechanisms of tissue angiogenesis and
                      to test new drug substances. A bioreactor made of PEEK was
                      developed, which enables direct imaging and perfusion.
                      Furthermore, different collagen- and fibrin-based hydrogels
                      were tailored to the different cell types, compared with
                      each other and the cell-ECM interactions were studied. The
                      results show the benefit of pure 2.5 $\%$ fibrin for
                      obtaining a stable endothelial layer as a lining for the
                      3D-bioprinted macrovessels. In contrast, collagen-fibrin
                      compositions with larger pores and less stiffness were
                      particularly suitable for tissue models of the liver and as
                      matrices of tumor spheroids. In particular, hepatocytes
                      showed an increased metabolic activity by an increased
                      production of albumin in the hydrogel that corresponded to
                      the stiffness of the healthy liver (4.5 kPa). It was also
                      shown, that the introduction of fibroblast and HUVECs into
                      the matrix had a positive influence on cell adhesion and
                      metabolism. HUVECs in the surrounding matrix increased the
                      formation of microvessels from the printed macrovessel. It
                      was advantageous if the printed HUVECs were first cultured
                      in the gelatine for three hours to adhere to the surrounding
                      matrix, before the gel was rinsed out. The endothelial layer
                      was significantly more stable if it had 72 hours to form
                      under static conditions before the flow through and thus the
                      dynamic cultivation started. Using the double sacrificial
                      material method, branched vascular structures up to a
                      diameter of 10 µm could be produced. The combination of the
                      developed in vitro model with a further developed liver and
                      the tumor model could provide new insights into the
                      metastatic cascade and subsequently for new approaches for
                      cancer therapy.},
      cin          = {542000-2 ; 937710 / 520000},
      ddc          = {620},
      cid          = {$I:(DE-82)542000-2_20140620$ / $I:(DE-82)520000_20140620$},
      typ          = {PUB:(DE-HGF)11},
      doi          = {10.18154/RWTH-2025-08995},
      url          = {https://publications.rwth-aachen.de/record/1020439},
}