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International Journal of Bioprinting                                  3D printing technology in neurotrauma




            proper bioinks for SLA-based 3D printing due to special   nerve repair. For example, microgel with sustained drug
            photocuring characteristics of printed biomaterials, and   release can be prepared by the DLP method. In addition,
            possible cytotoxicity of photoinitiator and uncured resin.  cells can be printed into microgel with high survival
                                                               and proliferation.  This approach offers a compelling
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            2.2.4. Digital light processing                    alternative to conventional methods for the neurotrauma.
            Digital light processing (DLP) is an advanced 3D printing   In summary, the DLP technology has garnered significant
            technology that utilizes digital micromirror devices   attention due to its precision, speed, and versatility, finding
            (DMD) to construct 3D objects by selectively solidifying   applications across fields of the neurotrauma. Nonetheless,
            light-sensitive polymers or other materials in a layer-by-  it has limitations, such as material compatibility and
            layer fashion.  The object is systematically built layer by   potential requirements for post-processing.
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            layer, with each layer solidified by the DMD projecting a
            2D image of the desired cross-section onto the liquid resin.   3. Three-dimensional printing strategies for
            When exposed to the light pattern, the photopolymer
            undergoes solidification, resulting in the formation   neurotrauma treatment
            of that specific layer of the object. After each layer is   External intervention is usually required to repair the
            solidified, the build platform incrementally moves upward,   damage following neurotrauma. Current 3D printing
            creating  space  for  the  subsequent  layer.  This  process   strategies for neurotrauma treatment mainly include
            iterates until the entire 3D structure is fully realized.   biomaterials, physical regulation, bioactive substances,
            DLP technology boasts numerous advantages, including   and cell transplantation. 3D printing can prepare
            rapid production, high precision, no artificial interfaces,   corresponding bulk hydrogels, microspheres, conduits, or
            absence of nozzles, and suitability for crafting intricate   microneedles to treat neurotrauma in combination with the
            structures. DLP technology shows great promise in the   above strategies. Figure 2 summarizes current 3D printing
            neurotrauma. On the one hand, DLP technology enables   strategies  for neurotrauma treatment.  Besides,  Tables  2
            the customization of patient-specific constructs with finely   and 3 list the detailed studies related to 3D printing for
            tuned structures. Its ability to create intricate hierarchal   neurotrauma treatment.
            branched geometries and achieve printing resolutions
            as fine as 1 μm represents a significant advancement in   3.1. Biomaterials
            bioprinting technology.  On the other hand, DLP can be   Biomaterials  can  bridge  damaged  areas  of  the  nervous
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            leveraged to create constructs that integrate nanoparticles   system, promote axon extension and cell migration, and
            and drugs, facilitating sustained drug release to enhance   be used as carriers of neurotrophic or regulatory drugs.






























            Figure 2. Schematic diagram of various treatment strategies for neurotrauma using 3D printing technology. Strategies such as biomaterial, physical
            regulation, bioactive substance, and cell transplantation are combined with various constructs of 3D printing from different angles to treat neurotrauma.
            At the same time, combinations of these strategies are increasingly common. The figure is generated with BioRender.com.


            Volume 10 Issue 3 (2024)                        67                                doi: 10.36922/ijb.2311
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