Chinese Journal of Tissue Engineering Research ›› 2024, Vol. 28 ›› Issue (17): 2631-2636.doi: 10.12307/2024.479

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Preparation of heparinized acellular vascular scaffold and hemocompatibility evaluation

Li Xiafei1, Zhao Lingling2, Liang Feng3, Zhang Xuewei2, Zhang Jinjin2, Lin Fei4, Yang Tuo2, Zhao Liang2   

  1. 1College of Medical Engineering, 2College of Life Science and Technology, 3Mingde College, Xinxiang Medical University, Xinxiang 453003, Henan Province, China; 4First Affiliated Hospital of Xinxiang Medical University, Xinxiang 453003, Henan Province, China
  • Received:2023-07-07 Accepted:2023-09-15 Online:2024-06-18 Published:2023-12-14
  • Contact: Zhao Liang, PhD, Associate professor, College of Life Science and Technology, Xinxiang Medical University, Xinxiang 453003, Henan Province, China
  • About author:Li Xiafei, Master, Experimentalist, College of Medical Engineering, Xinxiang Medical University, Xinxiang 453003, Henan Province, China
  • Supported by:
    Natural Science Foundation of Henan Province, No. 202300410311 (to ZL); College Student Innovation and Entrepreneurship Training Program Project of Henan Province, No. S202310472023 (to LF); Postgraduate Research and Innovation Support Plan Project of Xinxiang Medical University, No. YJSCX2022108Y (to YT); 2022 Research and Innovation of College Students in Xinxiang Medical University, No. xyxskyz202236 (to ZJJ); Employment and Entrepreneurship Project in Colleges and Universities in Henan Province, No. JYB2023039 (to ZL)

Abstract: BACKGROUND: Acellular vascular scaffolds can mimic the microstructure and function of native blood vessels, but some extracellular matrix loss occurs during their preparation, which affects their hemocompatibility. Therefore, it is necessary to modify them to improve their hemocompatibility.
OBJECTIVE: To assess the hemocompatibility of acellular vascular scaffold prepared by Triton-x100/heparin sodium treatment. 
METHODS: The abdominal aorta was taken from SD rats and randomly divided into control and experimental groups. The control group was treated with Triton-x100 for 48 hours. The experimental group was treated with Triton-x100 for 48 hours and then treated with heparin sodium. The morphology and hydrophilicity of the two groups of acellular vascular scaffolds were detected. The hemocompatibility of the two groups of acellular vascular scaffold was evaluated by recalcification coagulation time test, platelet adhesion test, dynamic coagulation time test, hemolysis test, and complement activation test. 
RESULTS AND CONCLUSION: (1) Scanning electron microscopy showed that the surface of the two groups of vascular scaffolds was relatively intact, and a large number of fiber filaments appeared on the surface of the scaffolds after decellularity treatment, and the surface microstructure changed significantly. The water contact angle of the two groups of vascular scaffolds was smaller than that of natural vessels (P < 0.000 1). There was no significant difference in water contact angle between the two groups (P > 0.05). (2) The coagulation time of vascular scaffold was longer in the experimental group than in the control group (P < 0.05). The number of platelets attached to the scaffold membrane was less in the experimental group than that in the control group (P < 0.000 1). The coagulation index was greater in the experimental group than that in the control group (P < 0.01), and the complement level was lower in the experimental group than that in the control group (P < 0.001). The hemolysis rate of the two groups was lower than 5% of the national standard. (3) To conclude, acellular scaffold treated with Triton-x100/heparin sodium has excellent hemocompatibility.

Key words: acellular vascular scaffold, heparinization, hemocompatibility, cardiovascular disease, tissue engineering

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