4.8 Article

Syntheses and characterization of anti-thrombotic and anti-oxidative Gastrodin-modified polyurethane for vascular tissue engineering

Journal

BIOACTIVE MATERIALS
Volume 6, Issue 2, Pages 404-419

Publisher

KEAI PUBLISHING LTD
DOI: 10.1016/j.bioactmat.2020.08.008

Keywords

Gastrodin; Polyurethane; Anti-coagulation; Anti-inflammation; Angiogenesis

Funding

  1. National Natural Science Foundation of China [81760087/31760292/81860326/81560050]
  2. Department of Science and Technology of Yunnan Province of China [2017FA035/2017FE467(-008)/2018FE001(-137)/2018FE001(165)/2018FE001(-125)/2018IA048/2019ZF011-2]
  3. Major Program of Kunming Science and Technology Innovation Center [2019-1-N-25318000003568]
  4. Program for Innovative Research Team (in Science and Technology) in University of Yunnan Province (IRTSTYN)

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A novel polyurethane elastomer incorporating anti-coagulative and anti-inflammatory agent Gastrodin was fabricated, showing potential to promote blood vessel regeneration and significantly improve blood cell compatibility and anti-coagulation response.
Vascular grafts must avoid negative inflammatory responses and thrombogenesis to prohibit fibrotic deposition immediately upon implantation and promote the regeneration of small diameter blood vessels (< 6 mm inner diameter). Here, polyurethane (PU) elastomers incorporating anti-coagulative and anti-inflammatory Gastrodin were fabricated. The films had inter-connected pores with porosities equal to or greater than 86% and pore sizes ranging from 250 to 400 mu m. Incorporation of Gastrodin into PU films resulted in desirable mechanical properties, hydrophilicity, swelling ratios and degradation rates without collapse. The released Gastrodin maintained bioactivity over 21 days as assessed by its anti-oxidative capability. The Gastrodin/PU had better anti-coagulation response (less observable BSA, fibrinogen and platelet adhesion/activation and suppressed clotting in whole blood). Red blood cell compatibility, measured by hemolysis, was greatly improved with 2Gastrodin/PU compared to other Gastrodin/PU groups. Notably, Gastrodin/PU upregulated anti-oxidant factors Nrf2 and HO-1 expression in H2O2 treated HUVECs, correlated with decreasing pro-inflammatory cytokines TNF-alpha and IL-1 beta in RAW 264.7 cells. Upon implantation in a subcutaneous pocket, PU was encapsulated by an obvious fibrous capsule, concurrent with a large amount of inflammatory cell infiltration, while Gastrodin/PU induced a thinner fibrous capsule, especially 2Gastrodin/PU. Further, enhanced adhesion and proliferation of HUVECs seeded onto films in vitro demonstrated that 2Gastrodin/PU could help cell recruitment, as evidenced by rapid host cell infiltration and substantial blood vessel formation in vivo. These results indicate that 2Gastrodin/PU has the potential to facilitate blood vessel regeneration, thus providing new insight into the development of clinically effective vascular grafts.

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