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International Journal of Bioprinting                             Skin bioprinting: Keratinocytes and stem cells




            for cell-laden Alg/HA/Gel constructs over 14 days, while a   Ethics approval and consent to participate
            degradation of 20% was observed for GelMA constructs,   Not applicable.
            highlighting the importance of optimizing the degradation
            rate in accordance with the tissue repair rate.  Depending   Consent for publication
                                                27
            on the type of wound, the cutaneous healing time can last up
                                                         16
                     17
            to 8 weeks.  Crosslinking delays the degradation process.    Not applicable.
            For instance, photo-crosslinking of GelMA produces a stable
            construct with slow degradation rates, making GelMA suitable   Availability of data
            for long-term applications.  During long-term incubation,   Data are available on request from the authors.
                                 19
            the rapid degradation rate of Alg/HA/Gel-based skin
            substitutes could limit its application, but this may be avoided   References
            by additional  crosslinking  of  Alg/HA/Gel  with microbial
            transglutaminase (mTG) to slow down degradation. 26  1.   Tottoli EM, Dorati R, Genta I, Chiesa E, Pisani S, Conti B. Skin
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                                                                  doi: 10.3390/pharmaceutics12080735
            Biofabricated potential skin substitutes made of GelMA
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            HaCaT    keratinocytes,  outperforming  bioprinted    the current state of bioprinted skin substitutes for wound
                                                                  healing. Biomedicines. 2023;11(10):2678.
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            These findings indicate that GelMA-based constructs with   3.   Zuo KJ, Medina A, Tredget EE. Important developments in
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                                                               4.   Wang Y, Beekman J, Hew J, et al. Burn injury: challenges
            Acknowledgments                                       and advances in burn wound healing, infection, pain and
                                                                  scarring. Adv Drug Deliv Rev. 2018;123:3-17.
            We would like to thank Stefan Fleischer for the excellent      doi: 10.1016/j.addr.2017.09.018
            technical assistance during the study.
                                                               5.   Jeschke MG, Shahrokhi S, Finnerty CC, Branski LK,
                                                                  Dibildox M. Wound coverage technologies in burn care:
            Funding                                               established techniques. J Burn Care Res. 2018;39(3):313-318.

            The   work   was   funded   by   the   Deutsche       doi: 10.1097/BCR.0b013e3182920d29
            Forschungsgemeinschaft  (DFG,  German  Research    6.   Varkey M, Visscher DO, van Zuijlen PPM, Atala A, Yoo JJ.
            Foundation;  project  number  326998133,  TRR  225;   Skin bioprinting: the future of burn wound reconstruction?
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                                                                  doi: 10.1186/s41038-019-0142-7
            Conflict of interest                               7.   Sorgel CA, Schmid R, Kengelbach-Weigand A, Promny T,
            The authors declare no conflict of interest.          Horch RE. Air-pressure-supported application of cultured
                                                                  human keratinocytes in a fibrin sealant suspension as a
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            Author contributions                                  2022;11(17):5032.
            Conceptualization: Rafael Schmid, Celena A. Sörgel     doi: 10.3390/jcm11175032
            Formal analysis: Eva Bettendorf, Rafael Schmid     8.   Tan SH, Ngo ZH, Sci DB, Leavesley D, Liang K. Recent
            Investigation:  Eva Bettendorf, Celena A. Sörgel,     advances in the design of three-dimensional and bioprinted
               Yvonne Kulike                                      scaffolds for full-thickness wound healing. Tissue Eng Part B
            Methodology: Rafael Schmid, Celena A. Sörgel          Rev. 2022;28(1):160-181.
            Resources: Stefan Schrüfer, Dirk W. Schubert, Zan      doi: 10.1089/ten.TEB.2020.0339
               Lamberger, Philipp Stahlhut, Gregor Lang, Raymund   9.   Weng T, Zhang W, Xia Y, et al. 3D bioprinting for skin tissue
               E. Horch                                           engineering: current status and perspectives. J Tissue Eng.
            Supervision: Raymund E. Horch, Celena A. Sörgel       2021;12:20417314211028574.
            Writing – original draft: Eva Bettendorf              doi: 10.1177/20417314211028574
            Writing  –  review  &  editing:  Eva Bettendorf, Annika   10.  Park J, Lee SJ, Chung S, et al. Cell-laden 3D bioprinting
               Kengelbach-Weigand, Rafael Schmid, Celena A. Sörgel  hydrogel matrix depending on different compositions for


            Volume 10 Issue 6 (2024)                       279                                doi: 10.36922/ijb.3925
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