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International Journal of Bioprinting                           3D bioprinting techniques & hydrogels materials




            combination with bioceramics in integrated osteochondral   Chen et al. combined a thixotropic magnesium
            repair are as follows:                                  phosphate-based hydrogel  material with  gellan/
            (i)   Hydroxyapatite (HAP): HAP, the most widely        alginate to produce bioink, and the printed scaffold
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                 used bioactive material in calcium carbonate       exhibited outstanding osteogenic activity.
                 ceramics, has outstanding biocompatibility and   (iii)  The combination of bioceramics and hydrogels as
                 mechanical properties, which  can compensate       bioinks holds significant potential for 3D printing in
                 for the deficiencies in the mechanical properties   osteochondral repair. However, the current number
                 of hydrogels. In addition, its porous structure    of studies is rather limited, warranting further
                 is conducive to the growth of bone tissue and      research to derive more precise conclusions.
                 vessels.  Recently, researchers have endeavored
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                 to print scaffolds appropriate for osteochondral   3.2.2. Synthetic polymer-reinforced hydrogels
                 repair  through the  combination  of hydrogels  and   Synthetic  polymers,  such  as  polycaprolactone  (PCL)
                 HAP. You et al. compared the biological properties   and polylactic acid (PLA), are extensively employed as
                 of pure alginate hydrogel scaffolds and alginate   tissue engineering materials due to their plasticity and
                 hydrogels combined with HAP composite scaffolds.   controllable degradation rate. These polymers are often
                 They discovered that chondrocytes exhibited a   combined with hydrogels to develop composite materials.
                 higher survival rate and proliferation efficiency in   Gao et al. combined poly(N-acryloyl 2-glycine) (PACG)
                 the composite scaffolds, as well as a higher level   and GelMA to develop a biodegradable, high-strength
                 of mineralized matrix, revealing their potential in   molecular polymer-reinforced biohybrid gradient
                 the integrated repair of osteochondral tissues.    scaffold that promoted the simultaneous regeneration
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                 Liu et al. employed a composite material consisting   of cartilage and subchondral bone in rats  (Figure 2ii).
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                 of GelMA and nanoHAP (nHAP) to fabricate      N-acryloyl glycinamide (NAGA) is also compounded
                 a three-layer scaffold for repairing OCDs in   into a GelMA hydrogel and printed as a scaffold,
                 rabbits and demonstrated a favorable therapeutic   which has great potential for treating OCDs under
                 effect  (Figure 2ii). Furthermore, Wang et al.   OA conditions and exhibits excellent antifatigue and
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                 reported  that  HAP content  and hypoxia are   antioxidation properties, as well as printability.  In
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                 important factors for osteogenic differentiation,   addition, Antich et al. utilized HA and PLA to print a
                 hypertrophy, and endochondrosis of adipose    composite scaffold with excellent mechanical properties
                 MSCs (ADMSCs), but the optimal HAP content    that can promote cartilage regeneration by increasing the
                 has not yet been determined.  HAP and hydrogel   expression of chondrogenic gene markers and specific
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                 composite scaffolds demonstrate great potential   matrix deposition. 165
                 in osteochondral repair, but the optimal ratio of
                 mixing is still uncertain, and further studies are   Due to the large amount of equipment required,
                 warranted to determine whether this combination   difficulties with bioink crosslinking, and other issues,
                 can enhance efficacy.                         traditional 3D bioprinting methods are generally printed
                                                               in vitro before implantation in the body to repair the
            (ii)  β-Tricalcium phosphate (TCP) and magnesium   damaged area. Its long waiting time without treatment
                 phosphate:  The  most  commonly  utilized  calcium   makes it a major flaw. As an emerging technology, in situ
                 phosphate derivative is TCP. Among its forms, β-TCP,   3D printing can be implemented to greatly reduce the
                 which has an inorganic composition similar to that   waiting time.  Ma et al. 3D printed a four-arm pegylated
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                 of the bone matrix, is widely used in biomaterials   hydrogel hybrid scaffold in situ with robotic assistance, and
                 due to  its ability to  effectively  bind to bone and   OCDs could be repaired in approximately 60 s. 167
                 ensure normal cell growth and differentiation. In
                 osteochondral  repair,  Kosik-Kozioł  et  al.  designed   Although many studies have explored the use of
                 a 3D hydrogel scaffold containing  β-TCP that can   polymer hydrogel composites in osteochondral integrative
                 promote the proliferation and differentiation of bone   repair, many problems remain in their clinical application.
                 marrow-derived MSCs (BMSCs) and reported that   For  example,  further  extensive  and clinical translational
                 0.5% w/v TCP was the optimal concentration for   research is required to determine how to better control
                 the formation of a stable scaffold.  Approximately   the degradation rate to match bone growth and identify
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                 60% of magnesium in the human body is found in   optimal porosity. Furthermore, while in situ 3D printing
                 the bone matrix, where it facilitates cell adhesion,   technology has begun to be applied, more relevant research
                 proliferation, and differentiation; induces bone   and better technology are needed to improve repair results
                 mineral deposition; and promotes bone formation.    in the future.
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            Volume 10 Issue 6 (2024)                        75                                doi: 10.36922/ijb.4472
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