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Fibrin-based Bioinks
           example, oxygen consumption, and changes in         revision  support  from  PS,  RS,  and  EB.  PS  and
           pH level. This approach was previously realized     VM coordinated the manuscript preparation. All
           using scaffolds, but  no study regarding  bioinks,   authors read and approved the final manuscript.
           particularly  fibrin-based  bioinks,  has  been
           performed.  For  instance,  O’Donnell  fabricated   Acknowledgments
           pH-sensitive  cellulose-based  scaffolds  labeled   This work was supported by the Russian Science
           through cellulose-binding domain with enhanced      Foundation (18-15-00407, general  information,
           cyan fluorescent protein . Such scaffolds ensured   applications,  biological  properties  and their
                                 [98]
           the analysis of extracellular acidification combined
           with probe-based monitoring of cell oxygenation.    tuning) and Russian academic excellence project
           Moreover, being “smart,” such bioinks may adapt     5–100 (trends).
           to  meet  cell  requirements  that  include  not  only   Conflicts of interest
           matrix  re-modeling  but  also bioactive  substance
           release.  Hence,  researchers  will  have  a  unique   The authors declare that they have no conflicts of
           in vitro platform for organ and tissue fabrication.  interest.
             Compared to the majority of biomaterials, fibrin
           can be autologously derived that is a significant   References
           advantage  for further clinical  translation  of the   1.   Antoshin AA, Churbanov SN, Minaev NV, et al., 2019, LIFT-
           bioprinted  constructs.  However,  the  fibrinogen
           concentration  in  blood  is relatively  low  in        bioprinting,  is  it  Worth  it?  Bioprinting,  15:e00052.  DOI:
           comparison with the used one for bioink preparation     10.1016/j.bprint.2019.e00052.
           (2 mg/ml  vs. 20 mg/ml ). Therefore, in recent      2.   Jiang T,  Munguia-Lopez  JG,  Flores-Torres  S,  et al.,  2019,
                                   [95]
                    [99]
           papers [87,100] , such bioinks were prepared not from   Extrusion Bioprinting  of Soft Materials:  An Emerging
           pure fibrinogen, but blood plasma.                      Technique for Biological Model Fabrication. Appl Phys Rev,
                                                                   6:011310. DOI: 10.1063/1.5059393.
           4 Conclusions                                       3.   Gudapati  H,  Dey  M,  Ozbolat  I,  2016,  A  Comprehensive
                                                                   Review on Droplet-based Bioprinting: Past, Present
           The development of bioprinting has inspired new         and  Future.  Biomaterials,  102:20–42.  DOI:  10.1016/j.
           applications of fibrin as a bioink. Compared to other   biomaterials.2016.06.012.
           biomaterials, fibrin can be autologously derived that   4.   Unagolla  JM,  Jayasuriya  AC,  2020,  Hydrogel-based
           facilitates its clinical translation and has significant   3D Bioprinting:  A  Comprehensive Review on Cell-
           intrinsic  properties  such  as  induction  of  wound   laden  Hydrogels,  Bioink  Formulations,  and  Future
           healing and angiogenesis that are highly valuable       Perspectives. Appl Mater Today, 18:100479. DOI: 10.1016/j.
           in tissue engineering. It also provides a possibility   apmt.2019.100479.
           for  fine  tuning  both  mechanical  and  biological   5.   Kurniawan  NA,  Van  Kempen  TH,  Sonneveld  S,  et al.,
           properties. Fibrin and its blends can be pioneering     2017, Buffers Strongly Modulate Fibrin Self-Assembly into
           in the development of smart bionks that provide not     Fibrous  Networks.  Langmuir,  33:6342–52.  DOI:  10.1021/
           only an adaptable cell-friendly microenvironment        acs.langmuir.7b00527.
           but also the information on cell functioning.       6.   Kurniawan NA, Grimbergen J, Koopman J, et al., 2014, Factor

           Authors’ contributions                                  XIII  Stiffens  Fibrin  Clots  by  Causing  Fiber  Compaction.
                                                                   J Thromb Haemost, 12:1687–96. DOI: 10.1111/jth.12705.
           AS,  VM,  and  PS  outlined  the  manuscript.       7.   Weisel JW, Litvinov RI, 2017, Fibrin Formation, Structure
           DO  contributed  to  “Fibrin  overview,”  YE  –         and Properties. Subcell Biochem, 82:405–56.
           “Mechanical properties,” PB, EB, and NK             8.   Kim  E,  Kim  OV,  Machlus  KR,  et  al.,  2011,  Correlation
           –  “Wound  healing,”  AS  and  ASo  -  “Trends”,        between Fibrin Network Structure and Mechanical Properties:
           and  RS,  ML,  and  MV  –  “Angiogenesis.”  AS          An Experimental and Computational Analysis. Soft Matter,
           drafted the manuscript with primary editing and         7:4983–92. DOI: 10.1039/c0sm01528h.

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