1. Academic Validation
  2. A 3D-printed scaffold composed of Alg/HA/SIS for the treatment of diabetic bone defects

A 3D-printed scaffold composed of Alg/HA/SIS for the treatment of diabetic bone defects

  • J Orthop Translat. 2024 Jul 25:48:25-38. doi: 10.1016/j.jot.2024.07.006.
Jie Tan 1 2 3 Zecai Chen 1 Zhen Xu 1 Yafang Huang 1 3 Lei Qin 1 Yufeng Long 1 Jiayi Wu 1 Wanrong Luo 1 Xuchao Liu 1 Weihong Yi 1 Huaiyu Wang 2 Dazhi Yang 1
Affiliations

Affiliations

  • 1 Department of Spine Surgery & Innovative Laboratory of Orthopedics, Huazhong University of Science and Technology Union Shenzhen Hospital, Shenzhen, Guangdong, 518052, China.
  • 2 Center for Human Tissues and Organs Degeneration, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, China.
  • 3 Orthopaedic Department, Wuhan Fourth Hospital, Wuhan, 430030, China.
Abstract

Background: Diabetic bone healing remains a great challenge due to its pathological features including biochemical disturbance, excessive inflammation, and reduced blood vessel formation. In previous studies, small intestine submucosa (SIS) has been demonstrated for its immunomodulatory and angiogenic properties, which are necessary to diabetic bone healing. However, the noticeable drawbacks of SIS such as fast degradation rate, slow gelling time, and weak mechanical property seriously impede the 3D printing of SIS for bone repair.

Method: In this study, we developed a novel kind of 3D-printed scaffold composed of alginate, nano-hydroxyapatite, and SIS. The morphological characterization, biocompatibility, and in vitro biological effects of the scaffolds were evaluated, and an established diabetic rat model was used for testing the in vivo biological effect of the scaffold after implantation.

Results: The in vitro and in vivo results show that the addition of SIS can tune the immunomodulatory properties and angiogenic and osteogenic performances of 3D-printed scaffold, where the macrophages polarization of M2 phenotype, migration and tube formation of HUVECs, as well as osteogenic expression of ALP, are all improved, which bode well with the functional requirements for treating diabetic bone nonunion. Furthermore, the incorporation of alginate substantially improves the printability of composites with tunable degradation properties, thereby broadening the application prospect of SIS-based Materials in the field of tissue engineering.

Conclusion: The fabricated 3D-printed Alg/HA/SIS scaffold provides desirable immunomodulatory effect, as well as good osteogenic and angiogenic performances in vitro and in vivo, which properties are well-suited with the requirement for treating diabetic bone defects.

Translational potential of this article: The incorporation of SIS and alginate acid not only provides good printability of the newly fabricated 3D-printed Alg/HA/SIS scaffold, but also improves its immunoregulatory and angiogenic properties, which suits well with the requirement for treating diabetic bone disease and opens up new horizons for the development of implants associating diabetic bone healings.

Keywords

Angiogenesis; Diabetic bone healing; Immunomodulation; Osteogenesis small intestinal submucosa.

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