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Horch et al.                                                                                                                                                                           Towards the future of plastic surgery





























           Figure 3: 3D negative imprint of angio- and vasculogenesis network   Figure 4: Future applications of 3D bioprinting envision a precise
           sprouting out from arterio-venous loop in an isolated chamber after   specialdeposition of cells and molecules into 3D scaffolds to
           6 weeks                                            mimick natural tissue conditions and to facilitate artificial tissue
                                                              replacement, such as in this artistic rendering an ear or a noise for
                                                              example, using tools of biofabrication
           tissue loss and tissue replacement. Therefore it is of
           no wonder that plastic surgeons who were engaged in
           replacing lost tissue were amongst the initial founders
           of what has then be termed tissue engineering (TE)
           and hence have been involved into all kinds of research
           in TE and regenerative medicine. Basically the initial
           idea of TE was to build appropriate scaffolds and then
           seed cells on such matrices to transplant them into the
           recipient area. In the laboratory considerable results
           have been obtained in generating replacement tissue
           but have not found their way into daily clinical practice
           yet. The main obstacle has turned out to be the lack of
           initial vascularization especially in large constructs [19] .
           These  suffer  from  sufficient  initial  blood  supply  after
           transplantation to nourish inherent or adherent cells
           right  from  the  beginning  of  their  inset.  One  possible
           way to overcome this problem is the prevascularization   Figure 5: 3D bioprinted ear frame work with bioink that can contain
           of  such  scaffolds utilizing  microsurgically  created   living cells to be positioned into the printed construct
           arterio-venous  (av-)  loops  to  three-dimensionally
           vascularize  large  constructs  before  the  designated   and  proteins  together  with  biodegradable  matrices
           cells are inoculated [Figure 3]. These prevascularized   [Figures 4 and 5], generally now perceived as the new
           constructs can then be successfully transplanted [20-23] .   field  of  “biofabrication” [29] . It has been postulated by
           Methods derived from such approaches have been     researchers that bioprinting would now be on the cusp
           successfully implemented into the clinical scenario [24-27] .   of entering the translational phase where laboratory
           For  the  first  time  in  the  literature  we  were  able  to   research practices can be scaled up into manufacturing
           successfully apply av-loops in two patients, fill in the   products specifically designed for individual patients [30] .
           patient´s own bone marrow stem cells, along with   In  addition  to  tissue  replacement  such  modalities
           a  hydroxyl-apatite  powder  and  fibrin  sealant  and   could  help  to  also  fight  systemic  conditions,  such  as
           we then have seen a permanent replacement and      diabetes mellitus or malignant diseases. With the help
           restoration of large human bone defects [28] . This is a   of biofabricated protein synthesizing producer cells
           very promising approach that offers a way from bench   in  a  3D  microvascularly  connected  defined  container
           to bedside already in selected cases. Latest advances   it can become possible to treat systemic or local
           now include the integration of 3D bioprinting of cells   diseaeses. The advantage of such containers with 3D
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