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Polydopamine-modified konjac glucomannan scaffold with sustained release of vascular endothelial growth factor to promote angiogenesis

  • Xulong Zhu
  • , Shuhan Wu
  • , Kuan Yang
  • , Wei Wei
  • , Yasir Aziz
  • , Wenjin Yuan
  • , Hideyuki Miyatake
  • , Yoshihiro Ito
  • , Zhao Wei
  • , Jianhui Li
  • , Yongmei Chen
  • Shaanxi Provincial People's Hospital
  • Xi'an Jiaotong University
  • Shaanxi University of Science and Technology
  • RIKEN

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

The fabrication of scaffolds capable of the sustained release of the vascular endothelial growth factor (VEGF) to promote angiogenesis for a long time remains a challenge in tissue engineering. Here, we report a facile approach for effectively fabricating a bioactive scaffold that gradually releases VEGF to promote angiogenesis. The scaffold was fabricated by coating polydopamine (PDA) on a konjac glucomannan (KGM) scaffold, followed by the surface immobilization of VEGF with PDA. The resulting VEGF-PDA/KGM scaffold, with a porous and interconnected microstructure (392 μm pore size with 84.80 porosity), combined the features of long-term biodegradability (10 weeks with 51 % degradation rate), excellent biocompatibility, and sustained VEGF release for up to 21 days. The bioactive VEGF-PDA/KGM scaffold exhibited multiple angiogenic activities over time, as confirmed by in vivo and in vitro experiments. For example, the scaffold significantly promoted the attachment and proliferation of human umbilical vein endothelial cells and the formation of vascular tubes in vitro. Moreover, the in vivo results demonstrated the formation and maturation of blood vessels after subcutaneous implantation in rats for four weeks. This promising strategy is a feasible approach for producing bioactive materials that can induce angiogenesis in vivo. These findings provide a new avenue for designing and fabricating biocompatible and long-term biodegradable scaffolds for sustained VEGF release to facilitate angiogenesis.

Original languageEnglish
Article number132333
JournalInternational Journal of Biological Macromolecules
Volume271
DOIs
StatePublished - Jun 2024

Keywords

  • Angiogenesis promotion
  • Growth factor release
  • PDA/KGM scaffold
  • VEGF immobilization

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