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In this study, freezing was used to separate a solute (polymer) and solvent (deionized water). The polymer in the ice crystals was then crosslinked with solvents, and this diminished the linear pores to form a porous structure. Gelatin and chitosan were blended and frozen, after which crosslinking agents were added, and the whole was frozen again and then freeze-dried to form chitosan/gelatin porous bone scaffolds. Stereomicroscopy, scanning electron microscopy, compressive strength testing, porosity testing, in vitro biocompatibility, and cytotoxicity were used to evaluate the properties of the bone scaffolds. The test results show that both crosslinking agents, glutaraldehyde (GA) and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide, were able to form a porous structure. In addition, the compressive strength increased as a result of the increased crosslinking time. However, the porosity and cell viability were not correlated with the crosslinking times. The optimal porous and interconnected pore structure occurred when the bone scaffolds were crosslinked with GA for 20 min. It was proven that crosslinking the frozen polymers successfully resulted in a division of the linear pores, and this resulted in interconnected multiple pores and a compressively strong structure. The 48-h cytotoxicity did not affect the cell viability. This study successfully produced chitosan/gelatin porous materials for biomaterials application.

This study proposes braid coronary stents with a form of reticular tube by using a braiding technique. Stainless steel fibers with a diameter of 0.08 mm and nitinol fibers are braided with various tooth numbers on the take-up gear and a specified tooth number on the braid gear with a hollow braiding technique in order to have different braiding angles. The resulting braids are then immersed in a polyvinyl alcohol solution in a custom-made mold to form braid coronary stents. A stereomicroscope is used to observe the cut section, a scanning electron microscope is used to examine the treatment for sharp points of the fibers, and Image Pro Plus software is used to analyze braiding angles and metal cover rate. The experiment results show that braiding angle influences the braiding structure; in addition, the larger the braiding angle, the less easily the fiber interaction points move. The immersion in polyvinyl alcohol solution can effectively bond the fiber interaction points, resulting in a better braiding structure. Metal cover rates are all below 20.9%. This study successfully creates novel braid coronary stents.

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In order to solve the incompatibility between high porosity and mechanical properties, this study fabricates bone scaffolds by combining braids and sodium alginate (SA) membranes. Polyethylene terephthalate (PET) plied yarns are braided into hollow, porous three dimensional (3D) PET braids, which are then immersed in SA solution, followed by cross-linking with calcium chloride (CaCl2) and drying, to form PET bone scaffolds. Next, SA membranes are rolled and then inserted into the braids to form the spiral and porous PET/SA bone scaffolds. Samples are finally evaluated for surface observation, porosity, water contact angle, compressive strength, and MTT assay. The test results show that the PET bone scaffolds and PET/SA bone scaffolds both have good hydrophilicity. An increasing number of layers and an increasing CaCl2 concentration cause the messy, loose surface structure to become neat and compact, which, in turn, decreases the porosity and increases the compressive strength. The MTT assay results show that the cell viability of differing SA membranes is beyond 100%, indicating that the PET/SA bone scaffolds containing SA membranes are biocompatible for cell attachment and proliferation.