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      A novel method for fabricating engineered structures with branched micro-channel using hollow hydrogel fibers

      1 , 1 , 2 , 1 , 1 , 1 , 1 , 2
      Biomicrofluidics
      AIP Publishing

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          Abstract

          <p class="first" id="d1822390e182">Vascularization plays a crucial role in the regeneration of different damaged or diseased tissues and organs. Vascularized networks bring sufficient nutrients and oxygen to implants and receptors. However, the fabrication of engineered structures with branched micro-channels (ESBM) is still the main technological barrier. To address this problem, this paper introduced a novel method for fabricating ESBM; the manufacturability and feasibility of this method was investigated. A triaxial nozzle with automatic cleaning function was mounted on a homemade 3D bioprinter to coaxially extrude sodium alginate (NaAlg) and calcium chloride (CaCl <sub>2</sub>) to form the hollow hydrogel fibers. With the incompleteness of cross-linking and proper trimming, ESBM could be produced rapidly. Different concentrations of NaAlg and CaCl <sub>2</sub> were used to produce ESBM, and mechanical property tests were conducted to confirm the optimal material concentration for making the branched structures. Cell media could be injected into the branched channel, which showed a good perfusion. Fibroblasts were able to maintain high viability after being cultured for a few days, which verified the non-cytotoxicity of the gelation and fabrication process. Thus, hollow hydrogel fibers were proved to be a potential method for fabricating micro-channels for vascularization. </p>

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          Most cited references29

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          Omnidirectional printing of 3D microvascular networks.

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            Engineering vascularized tissue.

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              Vascularized bone tissue engineering: approaches for potential improvement.

              Significant advances have been made in bone tissue engineering (TE) in the past decade. However, classical bone TE strategies have been hampered mainly due to the lack of vascularization within the engineered bone constructs, resulting in poor implant survival and integration. In an effort toward clinical success of engineered constructs, new TE concepts have arisen to develop bone substitutes that potentially mimic native bone tissue structure and function. Large tissue replacements have failed in the past due to the slow penetration of the host vasculature, leading to necrosis at the central region of the engineered tissues. For this reason, multiple microscale strategies have been developed to induce and incorporate vascular networks within engineered bone constructs before implantation in order to achieve successful integration with the host tissue. Previous attempts to engineer vascularized bone tissue only focused on the effect of a single component among the three main components of TE (scaffold, cells, or signaling cues) and have only achieved limited success. However, with efforts to improve the engineered bone tissue substitutes, bone TE approaches have become more complex by combining multiple strategies simultaneously. The driving force behind combining various TE strategies is to produce bone replacements that more closely recapitulate human physiology. Here, we review and discuss the limitations of current bone TE approaches and possible strategies to improve vascularization in bone tissue substitutes.
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                Author and article information

                Journal
                Biomicrofluidics
                Biomicrofluidics
                AIP Publishing
                1932-1058
                November 2016
                November 2016
                : 10
                : 6
                : 064104
                Affiliations
                [1 ]Rapid Manufacturing Engineering Center, Shanghai University, Shanghai 200444, People's Republic of China
                [2 ]Shanghai Key Laboratory of Intelligent Manufacturing and Robotics, Shanghai University, Shanghai 200072, People's Republic of China
                Article
                10.1063/1.4967456
                5116029
                27965729
                418fc10f-1617-411f-94b5-b7a17f96554b
                © 2016
                History

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