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International Journal of Bioprinting                     Decellularized  materials for bioprinting of liver constructs






































                                                                              [74]
            Figure 1. Crosslinking methods used in the synthesis of different kinds of hydrogels. Adapted from ref. , with copyright permission under the terms of
            the CC-BY-NC-ND 3.0 license.

            degradability, tuneability molecular weight, and material   polyethylene  glycol  (PEG),  polyethylene  oxide  (PEO),
            concentration must be optimized in the preprinting stages   polyvinylpyrrolidone (PVP), polylactic-glycolic acid
            to ensure efficient printability and reproducibility of the   (PLGA), polylactic acid (PLA), polycaprolactone (PCL),
            bioprinted products.                               and gelatin methacryloyl (GelMA) are commonly used
               Several  studies have  demonstrated  the  design  and   for 3D bioprinting applications [88,89] .
            synthesis of a wide variety of cytocompatible bioink   Arguably, recent advances in the design of a variety
            materials that can be printed alone as scaffolds or as   of  bio-interesting  materials  using  different  chemical,
            living cells embedded hydrogel for the 3D bioprinting of   physical, and enzymatic crosslinking strategies have
            spatially defined tissue constructs [73,80-87] . These bioink   enabled the formulation of several bioinks [90-92] .
            materials are mostly prepared from natural, synthetic,   Although bioinks based on natural and synthetic
            and semisynthetic polymer systems featuring typical   or semisynthetic materials are endowed with pro-
            native-like extracellular matrix (ECM)-mimicking   regenerative biophysiochemical attributes that are,
            features. Although commonly used natural biopolymers   to some extent, adaptable to the requirements of
            (e.g.,  alginate,  collagen,  chitosan,  gelatin,  hyaluronic   biologically active tissue regeneration, they are still
            acid, and agarose) offer biophysical and biochemical   far  from  ideal  bioinks  for  establishing  complex  tissue-
            resemblances with the native ECM; the printability,   engineered products for clinical applications (Figure 3).
            mechanical integrity, batch-to-batch variability, and   Poor cytocompatibility, anchorage-providing scaffolds,
            cell-adhesive properties of natural biopolymers are   cellular recognition, immunomodulation, and tissue-
            not  yet  fully  compatible  with  existing  bioprinting   specific degradation of synthetic materials are among
            modalities. Synthetic  bioinks, on  the  other hand,   the  limiting  factors  hindering  the  wider  application  of
            are generally synthesized by chemically modifying   synthetic polymers in the bioengineering of complex, and
            polymeric materials. Synthetic biomaterials are often   functional  hierarchical  structures.  Thus,  there  remains
            tailored with more supramolecular chemistries and   a significant tradeoff between the printing methods,
            mostly exhibit acceptable rheological, crosslinking,   the printing process efficiency, and the rheological and
            and gelling properties. Synthetic polymers such as   physicochemical parameters of bioinks .
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            Volume 9 Issue 3 (2023)                        343                          https://doi.org/10.18063/ijb.714
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