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      Surface modification of the biodegradable cardiovascular stent material Mg–Zn–Y–Nd alloy via conjugating REDV peptide for better endothelialization

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          Abstract

          Magnesium is a biodegradable material that has potential application in cardiovascular stent development: its excellent mechanical properties and blood compatibility make it highly useful in interventional therapy. Nevertheless, the following shortcomings restrict its further application: antihyperplasia function and promoting surface endothelialization. In this study, we immobilized a specific link peptide of endothelial cells, Arg-Glu-Asp-Val (REDV), onto polydopamine (PDA)-deposited Mg–Zn–Y–Nd alloy surface via covalent reaction to improve the growth of the endothelial cells. The PDA/REDV coating with optimized parameters maintained the good blood compatibility of the Mg–Zn–Y–Nd alloy at the biomimetic speed of the blood flow and significantly inhibited the growth of the vascular smooth muscle cells and macrophage attachment/activation, which indicated its better functions in antihyperplasia and anti-inflammation. In particular, the PDA/REDV coating not only showed consistent results in promoting the attachment of endothelial cells as reported elsewhere, but also displayed the ability of enhancing the viability of endothelial cells (or inhibiting apoptosis), suggesting its pro-endothelialized function through different pathways. In summary, this PDA/REDV coating addressed the above-mentioned shortcomings of the magnesium alloy, which may promise its wider application.

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          Novel Magnesium Alloys Developed for Biomedical Application: A Review

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            Coronary-artery stents.

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              Multifunctional Coating Based on Hyaluronic Acid and Dopamine Conjugate for Potential Application on Surface Modification of Cardiovascular Implanted Devices.

              Surface modification by conjugating biomolecules has been widely proved to enhance biocompatibility of cardiovascular implanted devices. Here, we aimed at developing a multifunctional surface that not only provides good hemocompatibility but also functions well in inducing desirable vascular cell-material interaction. In the present work, the multicoatings of hyaluronic acid (HA) and dopamine (PDA) were prepared onto 316L stainless steel (316L SS) via chemical conjugation (Michael addition, Schiff base reaction, and electrostatic adsorption). The results of platelet adhesion and activation and the whole blood tests indicated that the HA/PDA coatings obtained better hemocompatibility compared with the bare 316L SS and HA or PDA immobilized on 316L SS. The HA/PDA coatings also inhibited the proliferation of smooth muscle cells and adhesion/activation of macrophages effectively, whereas not all the HA/PDA coatings improved surface endothelialization rapidly and the effects of the multifunctional coatings on endothelial cell growth depend on the HA amounts (1.0, 2.0, and 5.0 mg/mL, labeled as PDA-HA-1, PDA-HA-2, and PDA-HA-5 respectively). Herein the PDA-HA-1 and PDA-HA-2 coatings were found to improve endothelial cell adhesion and proliferation significantly. The tissue compatibility of the HA/PDA coatings also depends on the HA amounts, and the PDA-HA-2 coating was proved to cause milder in vivo tissue response. Additionally, the mechanism of the HA molecular weight change and in vivo tissue response was also explored. These results effectively suggested that the HA/PDA coating might be promising when serving as a cardiovascular implanted device coating.
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                Author and article information

                Contributors
                Journal
                Journal of Materials Research
                J. Mater. Res.
                Springer Science and Business Media LLC
                0884-2914
                2044-5326
                December 14 2018
                November 06 2018
                December 14 2018
                : 33
                : 23
                : 4123-4133
                Article
                10.1557/jmr.2018.410
                c3333c7d-2bf6-4afc-ba70-6c04d3048020
                © 2018

                https://www.cambridge.org/core/terms

                https://www.cambridge.org/core/terms

                History

                Quantitative & Systems biology,Biophysics
                Quantitative & Systems biology, Biophysics

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