Page 97 - IJB-8-2
P. 97

Wang, et al.
                        A                                        B














                        C                                       D






















           Figure 5. Cell proliferation and morphology analysis of RASMCs seeded on different stents. (A) Live/dead staining images of RASMC-
           seeded stents after culture for 1 day and 7 days. (B) Cell proliferation of RASMCs after seeding on stents for days 1, 4 and 7. (C) F-actin
           (phalloidin, red) and DAPI (blue) staining of RASMCs after seeding on (C(i)) bare stents, (C(ii)) stents coated with dipyridamole-loaded
           poly(D,L-lactide) (PDLLA) nanofibers, and (C(iii)) stents coated with PDLLA/DP nanofibers for 7 days. (D) SEM images of RASMCs after
           seeding on (D(i)) bare stents, (D(ii)) stents coated with PDLLA nanofibers, and (D(iii)) stents coated with PDLLA/DP nanofibers for 7 days.
           Three samples (n = 3) from each group were used for cell proliferation evaluation. *P < 0.05, **P < 0.01.

           coated with DP-loaded nanofibers significantly reduced   causing blood vessels to return to a more natural state and
           the thickness of intimal hyperplasia compared with bare   recover  normal  vasomotion [1,3,33] .  DP-loaded  nanofibers
           stents, from 506 ± 153 μm to 288 ± 31 μm (Figure 7E).   showed  the  potential  for  long-term  drug  release  and
           Meanwhile,  the  average  neointimal  area  of  stents  with   could prevent SMC proliferation and have no detrimental
           DP-loaded  coating  was  decreased  by  54%  compared   effect on endothelial cells . Therefore, it is a promising
                                                                                    [21]
           to that of the bare stent group, decreasing from 2.14 ±   idea  to  develop  a  drug-loaded  bioresorbable  stent  by
           0.31 mm  to 0.98 ± 0.15 mm  (Figure 7F). The average   coating 3D-printed biodegradable stents with DP-loaded
                                   2
                  2
           neointimal stenosis ratio of stents with DP-loaded coating   nanofibers.
           was  remarkably  lower  (42%  vs.  65%)  than  that  of  the   To achieve the desired stent degradation and drug
           bare  stent  group  (Figure  7G). As  shown  in  Figure  9,   elution,  polymers  with  appropriate  degradation  rates
           after implantation for 28 days, CD31 expression around   and  biocompatibility  are  essential  to  act  as  backbone
           the bare PCL stents was lower than that around the DP-  materials and polymeric coatings. PCL has been widely
           loaded nanofibers coated stents.                    applied in biomedical applications because of its excellent

           4. Discussion                                       biocompatibility, flexible printability, suitable mechanical
                                                               properties,  and  appropriate  degradation  rate  (24  –
                                                                        [34]
           Ideally,  following  the  implantation  of  stents  into  the   36 months) . PDLLA has been widely used as a drug
           arteries, the sustained release of the drug should induce   delivery carrier because of its excellent biocompatibility
           the  inhibition  of  SMC  proliferation  and  allow  initial   and suitable degradation rate (9 – 24 months) [35,36] . Hence,
           endothelialization  with  the  rapid  degradation  of  the   PCL and PDLLA were selected to act as the backbone
           coating polymer material. Subsequently, as the backbone   material  of  the  stent  and  the  coating  polymer  in  the
           materials slowly degrade, the stent gradually disappears,   present work.

                                       International Journal of Bioprinting (2022)–Volume 8, Issue 2        89
   92   93   94   95   96   97   98   99   100   101   102