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Han X, et al.


























                                           Figure 7. the new version of the vascular system
           they are needed the most. The pore diameters were   consisted of three monomers plus a photoinitiator. The
           engineered to maximise the diffusion rate (yielding a   formulations are BPA-ethoxylated-diacrylate, lauryl
           lower pore diameter bound for pore radii range), support   acrylate and isobornylacrylate  (BLI) shown in Figure 9.
           angiogenesis, enable steady blood circulation inside the   Three types of photo-initiator were tested to select the
           vessels and maintain their manufacturability via AM   most appropriate one that has the lowest cytotoxicity.
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           system (yielding an upper pore diameter boundary). The   They are Irgacure  184, Irgacure  2959 and Irgacure
           conical pores were selected with larger outer diameter   369. BLI samples with three photoinitiators were
           pore diameter and smaller inner diameter. This type of   investigated by the two methods WST-1assay (three
           pore leads to a reduction of the pore diameter without   replicates of each kind of a material; characteristic of
           the formation of membranes. The design of the conical   the sample: diameter: 14 mm, height: 1–2 mm, weight:
           pore is shown in Figure 8.                          200 mg) and live/dead assay (characteristic of the
                                                               sample: diameter: 14 mm, height: 2–3 mm, weight:
           3. Material and Methods                             300 mg). All samples were disinfected in 70 % ethanol
                                                               for 30 min (meanwhile the samples swelled), washed
           3.1  Photocurable resin and photoinitiator          two times for 30 min with PBS and equilibrated in cell
                                                               culture medium. For both methods the mouse fibroblast
           The material selected in this work needs to have    cell line (3T3) was used, cultured in DMEM with
           appropriate viscosity and polymerisation characteristics   glutamine (Biochrome AG, Berlin, Germany) containing
           to allow it be printed successfully. Additionally, it also   10% fetal calf serum, 50 U/mL penicillin, and 50 µg/mL
           needs to have vessel-like properties, such as appropriate   streptomycin under 5% CO  atmosphere at 37 °C.
                                                                                      2
           elasticity, biocompatibility and surface readiness for   For live/dead assay the cells were seeded at
                                                                            2
           bio-coatability. The material chosen for this study   25,000 cells/cm , and after 1, 4 and 14 days, the cells


















                                    Figure 8. the design of the conical pore on the vascular vessel wall.

                                       International Journal of Bioprinting (2018)–Volume 4, Issue 2         7
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