Sequentially releasing self-healing hydrogel fabricated with TGFβ3-microspheres and bFGF to facilitate rat alveolar bone defect repair

Fenglin Yu; Dezhi Geng; Zhanpeng Kuang; Shiyi Huang; Yating Cheng; Yini Chen; Fang Leng; Yu Bei; Yueping Zhao; Qingxia Tang; Yadong Huang; Qi Xiang

doi:10.1016/j.ajps.2022.03.003

Sequentially releasing self-healing hydrogel fabricated with TGFβ3-microspheres and bFGF to facilitate rat alveolar bone defect repair

Asian J Pharm Sci. 2022 May;17(3):425-434. doi: 10.1016/j.ajps.2022.03.003. Epub 2022 Apr 13.

Authors

Fenglin Yu^{1

2

3}, Dezhi Geng^{1

2

3}, Zhanpeng Kuang^{1

2

3}, Shiyi Huang^{1

2

3}, Yating Cheng^{1

2

3}, Yini Chen^{1

2

3}, Fang Leng³, Yu Bei³, Yueping Zhao⁴, Qingxia Tang⁴, Yadong Huang^{1

2

3}, Qi Xiang^{1

2

3}

Affiliations

¹ Department of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.
² Guangdong Province Key Laboratory of Bioengineering Medicine, Jinan University, Guangzhou 510632, China.
³ Biopharmaceutical R&D Center of Jinan University, Guangzhou 510632, China.
⁴ Department of Stomatology, Jinan University Medical College, Guangzhou 510632, China.

Abstract

Resorption and loss of alveolar bone leads to oral dysfunction and loss of natural or implant teeth. Biomimetic delivery of growth factors based on stem cell recruitment and osteogenic differentiation, as the key steps in natural alveolar bone regenerative process, has been an area of intense research in recent years. A mesoporous self-healing hydrogel (DFH) with basic fibroblast growth factor (bFGF) entrapment and transforming growth factor β3 (TGFβ3) - loaded chitosan microspheres (CMs) was developed. The formulation was optimized by multiple tests of self-healing, in-bottle inversion, SEM, rheological, swelling rate and in vitro degradation. In vitro tubule formation assays, cell migration assays, and osteogenic differentiation assays confirmed the ability of DFH to promote blood vessels, recruit stem cells, and promote osteogenic differentiation. The optimum DFH formula is 0.05 ml 4Arm-PEG-DF (20%) added to 1 ml CsGlu (2%) containing bFGF (80 ng) and TGFβ3-microspheres (5 mg). The results of in vitro release studied by Elisa kit, indicated an 95% release of bFGF in 7 d and long-term sustained release of TGFβ3. For alveolar defects rat models, the expression levels of CD29 and CD45, the bone volume fraction, trabecular number, and trabecular thickness of new bone monitored by Micro-CT in DFH treatment groups were significantly higher than others (*P < 0.05, vs Model). HE and Masson staining show the same results. In conclusion, DFH is a design of bionic alveolar remodelling microenvironment, that is in early time microvessels formed by bFGF provide nutritious to recruited endogenous stem cells, then TGFβ3 slowly released speed up the process of new bones formation to common facilitate rat alveolar defect repair. The DFH with higher regenerative efficiency dovetails nicely with great demand due to the requirement of complicated biological processes.

Keywords: Alveolar defects; Self-healing hydrogel; Sequential release; TGFβ3 microspheres; bFGF.