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International Journal of Bioprinting                      Coronary and peripheral artery disease. State of the art.










































            Figure 2. (A) Classification of VS based on their degradability, type of blood vessel (to treat CAD or PAD) and implantation methodology. (B)  Relative
            amount of VS commercially available in the market. BRS stands for “bioresorbable stents,” SS “stainless steel,” SE “self-expandable stent,” and DES
            “drug-eluting stent.” The sector graph is drawn according to the information available in Table 1.
               Bioresorbable (BRS) VS are made of biodegradable   (paclitaxel,  actinomycin  D),  immunosuppressive
            materials, which can be degraded over time under   (sirolimus) and anti-inflammatory (dexamethasone)
            physiologic conditions until total disappearance. For a   drugs . The use of paclitaxel has been particularly useful
                                                                   [18]
            proper functioning, total BRS VS degradation must occur   in the prevention of in-stent restenosis according to [8].
            at a desirable, predictable rate, leaving behind a native   Recently, the review of Beshchasna  et  al. has reported
            vascular vessel fully repaired [15,17] . In fact, the control   that nanoparticles and genes can also be loaded into
            and prediction of their biodegradation rate is still the   DES . Therefore, DES are considered Modified Drug
                                                                  [15]
            main challenge in the production and improvement of   Delivery Systems (MDDS) since they must protect, carry,
            this group of VS. Despite some exceptions such as BRS   and  control  drug  release  toward  the  vessel  walls  or  the
            metallic stents made of Mg, Ti, and Zn, biodegradability is   bloodstream. These medical devices are commonly made
            a property usually associated to substances and molecules   of drug–polymer coating or direct drug immobilization
            with poorer mechanical properties than metals (polymers).   on  the  stent  surface [15,18] .  The  most  common  techniques
            This means that the major part of the ingredients used for   to load drugs on stent struts are spray coating and dip
            the production of BRS VS undertake poorer mechanical   coating. Regarding spray coating, a nozzle, which creates
            support when compared with BMS .                   droplets of approximately 10 μm in diameter, sprays the
                                        [12]
                                                               drug solution or drug/polymer composite solution over the
               DES are VS that carry active substances in their   stent struts. For dip coating, the whole stent is dipped into
            structure, which are progressively released to obtain a   the drug or drug/polymer solution in repeated occasions.
            certain therapeutic effect. DES prevent or reduce some   The excess of material over the stent is then removed by
            of the BMS side effects: thrombosis, neointimal scar   spinning or other techniques . DES can be differentiated
                                                                                      [19]
            tissue formation, restenosis, etc. In addition to the main   into first and second generation or third generation, with
            active substances loaded into DES, other substances also   the former one including non-bioresorbable DES and the
            include antithrombotic drugs (heparin), antiproliferative   latter one belonging to BRS DES .
                                                                                         [15]

            Volume 9 Issue 2 (2023)                        225                     https://doi.org/10.18063/ijb.v9i2.664
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