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International Journal of Bioprinting                                 FeS /PCL scaffold for bone regeneration
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            self-repair without forming scar tissue when fractured   piezoelectric,  or  microvalve  processes .  Although  this
                                                                                              [19]
            through the bone healing process . This process is based   technique is relatively inexpensive and has high printing
                                       [4]
            on a cascade of events, which include the restoration of   speeds, there are some limitations, such as limited bioink
            vascularity, recruitment of adjacent cells, ossification, etc. .    viscosity and rapid drying of the bioink post-ejection. In
                                                        [5]
            However,  in  severe  bone  fractures,  the  bone  healing   the case of laser-assisted systems, laser is used as the energy
            process might be disrupted. In order to aid the healing   source to deposit bioink . Using laser-based methods,
                                                                                   [20]
            of severe bone fractures, the use of bone grafts, such as   high printing resolution can be achieved. However, only
            autografts, allografts, and xenografts, has been considered   photo-crosslinkable bioinks can be used. One of the most
            as the ideal method . However, issues including the lack   common 3DBP techniques is extrusion-based method,
                            [6]
            of donors, donor site morbidity, and possibility of infection   where the bioink is extruded using pneumatic pressure or
            still prevail since these grafts are donor tissues [7-9] .   mechanical force . Extrusion-based systems compensates
                                                                            [21]
               These shortcomings have compelled the search for an   for the limitations of inkjet and laser-based methods. By
            alternative, leading to the development of a new field—tissue   utilizing the extrusion-based method, heterogeneous
            engineering. This field aims to restore or replace damaged   structures can be fabricated using various types of
            tissues or organs based on the development of biological   biomaterials. Another advantage is that extrusion-based
            substitutes . Viable cells, scaffolds, and growth factors   systems are highly customizable, and recently, they have
                    [10]
            are used to induce tissue development. The bioengineered   become more affordable.
            scaffolds should provide an environment similar to the   Various biomaterials such as ceramics, metals, and
            native tissue or organ  to enable the maturation of  cells   synthetic polymers have been used to develop tissue-
            into functional tissue or organ . Therefore, the chemical   engineered scaffolds for bone tissue regeneration [22-24] .
                                    [11]
            composition and physical structure should be carefully   Regardless of their benefits, these biomaterials do not mimic
            determined depending on the target tissue. Some of the   the properties of natural bone tissue. Most metals are not
            important characteristics that scaffolds should have for   biodegradable, ceramics are very brittle, and most of the
            bone  tissue  engineering  applications  include  mechanical   synthetic polymers are non-osteoconductive [25-27] . In order
            properties matching those of the host tissue, fully   to address these problems, blends of synthetic polymers and
            interconnected porous structure, and surface properties in   ceramics have been extensively investigated, benefitting
            favor of cell adhesion, proliferation, and differentiation .   from the favorable properties of each material. Since the
                                                       [12]
               Tissue-engineered scaffolds can be fabricated using   main components of bone are composed of ceramic-based
            various techniques. Recently, there has been extensive   materials, ceramics have been used in various regenerative
            research on three-dimensional (3D) bioprinting (3DBP),   applications . Moreover, the modifiability of synthetic
                                                                        [23]
                                                                                                           [28]
            which enables the fabrication of complex 3D structures   polymers offers a wide variety of applications (Table 1) .
            mimicking the native extracellular matrix structure.   Liu  et al. fabricated a composite scaffold composed of
            The most commonly used 3DBP techniques are inkjet,   poly(e-caprolactone) (PCL) and strontium-containing
            laser, and extrusion [13-18] . In inkjet printing, the solution   hydroxyapatite (SrHA) using a 3D printing method for
                                                                                  [29]
            is dispensed in the form of droplets through thermal,   bone tissue regeneration . The incorporation of SrHA not

      AQ2   Table 1. Previous works on polymer/bioceramic-based composite scaffolds for bone tissue regeneration

             Materials       Mechanical properties  Defect model    Degree of bone formation             Ref.
             PCL/SrHA        Increased with the addition    Rat skull defect  The repair performance of the PCL/SrHA scaffold was   [29]
                             of SrHA to PCL                         better than the control group
             PCL/nHA         Compressive modulus:  Rabbit calvarial defect  Percentage of defect reduction: 11.2%  [30]
                             109.6 ± 2.0 MPa
             Bioglass/mMCS/  Compressive modulus:  Rabbit femoral defect  Percentage of new bone area: 80%  [31]
             GA/PCL          12.1 ± 2.1 MPa
             PCL/silica      Compressive modulus:  Rat calvarial defect  Percentage of new bone area: 19%  [32]
                             26.0 ± 2.2 MPa
             dECM-coated CS/PCL  N/A              Rat calvarial defect  BT/TV value of 37.75%            [33]
             Mg-P/KR-34839   N/A                  Rat calvarial defect  Newly formed bone increased by 2.3-fold  [34]
            Abbreviations: BT/TV, bone volume per tissue volume; CS, calcium silicate; dECM, decellularized extracellular matrix; GA, gliadin; Mg-P,
            Magnesium phosphate; mMCS, mesoporous bioglass fibers of magnesium calcium silicate; nHA, nano-hydroxyapatite; PCL, polycaprolactone;
            SrHA, strontium- containing hydroxyapatite.


            Volume 9 Issue 1 (2023)olume 9 Issue 1 (2023)
            V                                              200                      https://doi.org/10.18063/ijb.v9i1.636
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