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A Scientometric Analysis
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           Figure 4. The application of bioprinting to fabricate vascularization and skin. (A) Schematic representation of the (i) bioprinting process of
           a multilayered vascularized construct. (ii) Fluorescence micrographs showing the endothelialization of the void spaces (created as a result
           of using permanent and sacrificial inks during the bioprinting process) and cross-sections showing a lumen. Adapted from Ouyang et al.,
           2020 , licensed under Creative Commons Attribution 4.0 International License. (B) A strategy to promote angiogenesis based on the use of
              [48]
           (i) a sacrificial ink that renders a channel and (ii) cell-degradable ink. (iii) Microscopy analysis showing the endothelialization of the channel
           and the angiogenic sprouting within the cell-degradable hydrogel. Magnifications show the presence of lumen structures (as small as
           ~10 µ) and the three-dimensional architecture . Reprinted (adapted) from Song KH, Highley CB, Rouff A, et al., Adv Funct Mater, 2018,
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           28(31):1–10. At 2018 WILEY-VCH Verlag GmbH Co. KGaA, Weinheim. (C) Schematic representation of the (i) bioprinting design of a
           multilayered skin construct. (ii) Experimental program involving skin bioprinting, implantation, explantation, and analysis. (iii) Histological
           micrographs showing the multilayered architecture and dermal markers of expression in human skin (for reference), grafted bioprinted skin
           without placental pericytes (PCs), and grafted bioprinted skin with PCs in the dermal bioink. EC: Endothelial cells. Adapted from Baltazar
           et al., 2020, Tissue Engineering Part A, 26: 5-6 . The publisher for this copyrighted material is Mary Ann Liebert, Inc. publishers.
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           critical situation faced by one million patients worldwide   demonstrates  the feasibility  of 3D printing  a full-size
           each year, as estimated  by the outage management   human heart made entirely of alginate (not yet including
           system . In the USA alone, 103,655 patients will    cells). To do this, the authors used Freeform Reversible
                [68]
           be waiting for an organ by 2020; these include 91,790   Embedding  of Suspended Hydrogels (FRESH), an
           patients in need of a kidney, 12,521 needing a liver, and   emerging  extrusion-based  technique  that  enables  the
           3504 needing a heart .  These are all highly complex   printing of practically any shape by injecting a hydrogel
                             [69]
           organs, not only in terms of their architecture and cell   into a thermo-reversible support bath. However, FRESH
           type  composition but  also  because  of their  size  and   (and any currently available bioprinting technique) has
           function.  Major organ fabrication  through  bioprinting   its limitation in its ability to fabricate full-size functional
           (or through any other  fabrication  technique)  remains   tissues. For example, printing this non-cellularized and
           a  major  unsolved  challenge [70,71] . A  recent  contribution   non-structured heart took 4 days .
                                                                                          [71]

           72                          International Journal of Bioprinting (2021)–Volume 7, Issue 2
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