References
1. Talygin E.A., Zhorzholiani Sh.T., Tkhagapsova M.M., Tsygankov Y.M., Agafonov A.V., Gorodkov A.Y., et al. Reconstruction of swirling blood flow in the heart and aorta on the basis of measurements of dynamic geometry and elastic properties of the flow channel. In: Vol. 3: Biomedical and Biotechnology Engineering. American Society of Mechanical Engineers, 2018.
2. Zhorzholiani S.T., Mironov A.A., Talygin E.A., Tsyga-nokov Yu.M., Agafonov A.V., Kiknadze G.I., et al. Analysis of dynamic geometric configuration of the aortic channel from the perspective of tornado-like flow organization of blood flow. Bull Exp Biol Med. 2018; 164 (4): 514-8.
3. Apostolakis I.Z., McGarry M.D., Bunting E.A., et al. Pulse wave imaging using coherent compounding in a phantom and in vivo. Phys Med Biol. 2017; 62 (5): 1700.
4. Chen Q., Wang Y., Zhi-Yong L. Re-examination of the mechanical anisotropy of porcine thoracic aorta by uniaxial tensile tests. Biomed Eng Online. 2016; 15 (2): 167.
5. Schlicht M.S., Khanafer K., Duprey A., et al. Experimental foundation for in vivo measurement of the elasticity of the aorta in computed tomography angiography. Eur J Vasc Endovasc Surg. 2013; 46 (6): 447.
6. Lee J.H., Oh S.H., Kim W.G. MMA/MPEOMA/VSA copolymer as a novel blood-compatible material: ex vivo platelet adhesion study. J Mater Sci Mater Med. 2004; 15: 155-9.
7. Yahye M., Martin K., Robert G. Acute thromboge-nicity of intact and injured natural blood conduits versus synthetic conduits: neutrophil, platelet, and fibrin(ogen) adsorption under various shear-rate conditions. J Biomed Mater Res. 1997; 34 (4): 477-85.
8. Zhorzholiani Sh.T., Talygin E.A., Krasheninni-kov S.V., Tsigankov Y.M., et al. Elasticity change along the aorta is a mechanism for supporting the physiological self-organization of tornado-like blood flow. Hum Physiol. 2018; 44 (5): 532-40.
9. Tsygankov Y.M., Zhorzholiani S.T., Khugaev G.A., et al. The effect of mechanical properties of synthetic prostheses made by electrospinning on the results of experimental implantation in the infrarenal abdominal aorta. Ann Vasc Surg. 2021; 70: 506-16.
10. Dobrova N.B., Noskova T.I., Novikova S.P., Gorodkov A.Yu. Collection of guidelines for assessing the bio compatible properties of artificial materials in contact with blood. In: Committee on New Medical Technology of the USSR Ministry of Health. Moscow, 1991: 70 p. (in Russian)
11. Daum R., Visser D., Wild C., et al. Fibronectin adsorption on electrospun synthetic vascular grafts attracts endothelial progenitor cells and promotes endothe-lialization in dynamic in vitro culture. Cells. 2020; 9 (3): 778.
12. Gostev АА Shundrina I.K., Pastukhov V.I., et al. In vivo stability of polyurethane-based electrospun vascular grafts in terms of chemistry and mechanics. Polymers. 2020; 12 (4): 845.
13. EUROGUIDE. On the accommodation and care of animals used for experimental and other scientific purposes. London: FELASA: Federation of European Laboratory Animal Science Associations, 2007.
14. European Convention for the Protection of Vertebrate Animals used for Experimental and Other Scientific Purposes EST No. 123. Strasbourg, 18.03.1986.
15. Sidorenko E.S. Methodology for the assessment of hemocompatible implantable materials. Vestnik RUDN. Seriya: Ekologiya i bezopasnost’ zhiznedeaytel’nosti [Bulletin of the Russian University of Peoples’ Friendship. Series: Ecology and Life Safety]. 2005; 1 (11): 109-12. (in Russian)
16. Cuenca J.P., Padalhin A., Lee B.-T. Small-diameter decellularized vascular graft with electrospun polycap-rolactone. Mater Lett. 2021; 284 (pt 2): 128973.
17. Zhao L., Li X., Yang L., et al. Evaluation of remodeling and regeneration of electrospun PCL/fibrin vascular grafts in vivo. Mater Sci Eng C Mater Biol Appl. 2021; 118: 111441.
18. Singh С., Wong C.S., Wang X. Medical textiles as vascular implants and their success to mimic natural arteries. J Funct Biomater. 2015; 6: 500-25.