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International Journal of Bioprinting                           3D-printed PPDO/GO stents for CHD treatment.












































            Figure 6. In vitro hemocompatibility of PPDO/GO stents. (a) Photograph of hemolysis test. (b) Hemolysis rate of different samples. (c) Number of
            adhered platelets per unit area on the surface of the stents. *p <0.05, ***p < 0.001. (d–f) SEM images of platelets adhered to the surface of the stents: (d)
            PPDO; (e) PPDO/0.2%GO; and (f) PPDO/0.5%GO. Scale bars: 20 μm. Abbreviations: GO, graphene oxide; PPDO, poly(p-dioxanone); SEM, scanning
            electron microscopy.



               Stent implantation inevitably damages the endothelium,   also observed in PPDO/GO groups. After 7 days of culture,
            a physical barrier between blood and vascular tissues that   HUVECs form a confluent layer in PPDO/GO groups
            is composed of endothelial cells (ECs). ECs secrete a series   (Figure 7b). These results indicate that PPDO/GO stents
            of substances, including anticoagulation molecules, nitric   are not cytotoxic to HUVECs and enhance their adhesion
            oxide, etc., to prevent thrombosis, inflammation, and in-  and proliferation. The π-electron cloud of graphene
            stent restenosis, and to restore vasomotion. 96,97  In order   interacts  with  the  hydrophobic  cores  of  proteins,  while
            to realize endothelialization, ECs have to  adhere and   the  high-density oxygen-containing  groups  of  GO  bind
            proliferate on the surface of stents. Here, the endothelial   with serum proteins through electrostatic interactions.
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            cytocompatibility of PPDO/GO stents is evaluated by   Serum proteins, including fibronectin and insulin, directly
            CCK-8 assay and immunofluorescence staining. After 1, 3,   mediate cell adhesion and morphology.  Additionally,
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            5, and 7 days of culture with HUVECs, all stents support   the incorporation of GO increases hydrophilicity, which
            the adhesion and growth of HUVECs, and the number of   may also contribute to protein loading, thereby enhancing
            cells increases with time (Figure 7a). The HUVECs on all   cell  adhesion and  proliferation. Results  of  cell count  of
            stents display a typical cobblestone morphology with large   fluorescence images (Figure 7c) indicate that the number
            nuclei and normal cytoskeleton organization (Figure 7b).    of HUVECs in the PPDO/0.5%GO group is significantly
            According  to  the  quantitative  results  of  the  CCK-8   greater than that of the PPDO/0.2%GO group after 3, 5,
            assay and fluorescence images (Figure 7a–c), there is a   and 7 days of culture. The proliferation rate of HUVECs
            significant statistical difference in the number of HUVECs   also demonstrates a similar trend. This dosage-dependency
            after 1, 3, 5, and 7 days of culture between PPDO/GO  and   of GO on cell adhesion and proliferation in a relatively
            pristine PPDO groups. An increased proliferation rate is   low range of GO content has also been reported in other


            Volume 10 Issue 6 (2024)                       328                                doi: 10.36922/ijb.4530
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