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International Journal of Bioprinting                              Design and property of PLPG/PDLA scaffold




            2. Materials and methods                              The  PLPG/PDLA  scaffolds  were  fabricated  using  a
                                                               3D bioprinter (Beijing Advanced Medical Technologies
            2.1. Materials                                     Inc., Beijing, China). The job program was designed in
            L-lactic acid (LLA), D-lactic acid (D-LA), and GA were
            obtained from Jinan Daigang Biomaterial (China).   SolidWorks and saved in STL format. To ensure good
            p-Dioxanone (PDO) was sourced from Bangcheng Chems   porosity, the fiber diameter and layer spacing of the PLPG/
            (China), and Sn(Oct)  was purchased from Adamas    PDLA scaffolds were set to 300 µm.
                               2
            Reagent Co. Ltd. (China).                             The preparation and manufacturing process of the
                                                               PLPG/PDLA scaffolds is illustrated in Scheme 1.
            2.2. Preparation of the PLPG copolymers
            The PLPG copolymers with a molar ratio of 90:5:5 for LLA,   2.4. Characterization of the PLPG/PDLA scaffolds
            GA, and PDO were synthesized using the same method   The surface morphology of the PLPG/PDLA scaffolds was
            described in our previously published article.  Specifically,   examined using scanning electron microscopy (SEM). The
                                               29
            the PLPG copolymers were prepared by ring-opening   porosity of the scaffolds was calculated using the ethanol
            polymerization of the following amounts: 184 g of LLA,   liquid displacement method according to Equation I:
            8.3 g of GA, and 7.3 g of PDO. Sn(Oct)  was used as the
                                            2
            catalyst, and the polymerization process was conducted
            at 135°C for three days. The resulting copolymers were      Porosity (%)      100              (I)
            treated with  dichloromethane  (CH Cl )  and  precipitated
                                           2
                                         2
            with ethanol. Finally, the obtained PLPG copolymers were
            dried at 70°C until their mass remained unchanged.    where V  and V refer to the ethanol volume before and
                                                                        1
                                                                              2
                                                               after  soaking  in  the PLPG/PDLA scaffolds, respectively,
            2.3. Fabrication of the PLPG/PDLA scaffolds        while V  represents the ethanol volume after wiping off the
                                                                     3
            The synthesized PLPG and PDLA polymers were        scaffolds. Each experiment had three parallel samples.
            thoroughly dissolved in CH Cl  for 0.5 h. The resulting
                                     2
                                   2
            solutions were then placed at 30°C until the solvent   2.5. Mechanical performance of the
            evaporated. The PLPG/PDLA composites were placed   PLPG/PDLA scaffolds
            in a vacuum-drying oven until their mass stabilized and   The mechanical performance of the PLPG/PDLA scaffolds
            were subsequently cut into pellets. Later, the PLPG/PDLA   (5 × 5 × 5 mm ) was measured using a static and dynamic
                                                                          3
            pellets were processed into powders using a wall crusher.  material testing machine (CMT2502; Shandong Wanchen





























            Scheme 1. Schematic illustration of the fabrication of PLPG/PDLA scaffolds for bone regeneration. Abbreviations: PDO: p-Dioxanone; PLLA:
            Poly(L-lactic acid); GA: Glycolic acid; PDLA: Poly(D-lactic acid); PLPG: PLLA-ran-PDO-ran-GA.


            Volume 10 Issue 6 (2024)                       534                                doi: 10.36922/ijb.4645
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