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International Journal of Bioprinting                                    3D bioprinting of collagen hydrogels











































            Figure 2. Characterization of the collagen biomaterial ink (CML-Ink). (A) Printability zone of the CML-Ink. (B) Gum-forming properties of the collagen
            solution (Col) and CML-Ink. (C) Extrudability of the CML-Ink. (D) Stability and uniformity of the CML-Ink. (E) A multi-step rheological test of Col
            and the CML-Ink. (F) Extrudable performance of Col and the CML-Ink. (G) Viscosity of Col and the CML-Ink at different shear rates. (H) Dynamic step
            strain amplitude test of Col and the CML-Ink. Abbreviations: MA: Methacrylic anhydride; LAP: Lithium phenyl-2,4,6-trimethylbenzoylphosphinate; Gʹ:
            Storage modulus; G˝: Loss modulus.

            increased significantly, with Gʹ rising by 14 times compared   as the shear rate increased. The CML-Ink exhibited a
            to its pre-illumination level. In contrast, Col maintained   linear decrease, suggesting stable shear thinning behavior
            constant values of Gʹ and G˝ before and after illumination.   across the tested range and suitability for extruded
            These findings indicate that the mechanical strength of the   3D printing.
            CML-Ink substantially improved following illumination at
            405 nm.                                               A dynamic step strain amplitude test (γ = 1.0 or 300%)
                                                               was carried out at 25 °C to replicate the extrusion process of
               The Col and CML-Ink were loaded into the syringe   Col and the CML-Ink in a syringe through continuous step
            used for 3D printing, with consistent extrusion speed   changes of oscillating strain (Figure 2H). Upon application
            and needle size, adhering to the printing conditions. The   of high strain (300%), the internal structure of both Col
            extrusion pressure experiment was carried out at room   and the CML-Ink was immediately disrupted, leading to a
            temperature to determine the extrudable performance   decrease in Gʹ to approximately 9 and 21 Pa, respectively,
            of the prepared ink (Figure 2F). Col exhibited noticeable   with Gʹ becoming lesser than G˝ and exhibiting a sol-like
            fluctuations in the pushing force required during the   appearance. However, upon reduction to low strain (1%),
            extrusion process. In contrast, the CML-Ink could be   the Gʹ  and G˝ of both  materials  almost fully recovered
            consistently extruded as a uniform fine filament with a   within a few seconds, with Gʹ surpassing G˝ and displaying
            pushing force of approximately 15 N, indicating its stable   a gel-like appearance. Both Col and CML-Ink demonstrated
            extrudable performance and suitability for 3D printing.  rapid sol-gel conversion ability during the three rupture
               The dynamic viscosities of Col and the CML-Ink were   and reforming cycles, indicating their ability to swiftly
            measured at 25 °C across shear rates of 0.1–100 s  (Figure   transition to a sol state during syringe extrusion and return
                                                   −1
            2G). The viscosity of both Col and the CML-Ink decreased   to the pre-extrusion gel state immediately afterward.

            Volume 10 Issue 5 (2024)                       549                                doi: 10.36922/ijb.4069
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