» Articles » PMID: 35663398

AM1241-Loaded Poly(ethylene Glycol)-Dithiothreitol Hydrogel Repairs Cranial Bone Defects by Promoting Vascular Endothelial Growth Factor and COL-1 Expression

Overview
Specialty Cell Biology
Date 2022 Jun 6
PMID 35663398
Authors
Affiliations
Soon will be listed here.
Abstract

To explore the repair effect of the prepared drug-loaded AM1241 poly(ethylene glycol)-dithiothreitol (PEG-DTT) hydrogel on cranial bone defects in SD rats. The PEG-DTT hydrogel under borax catalysis was quickly prepared, and the characterization of the material was observed by a scanning electron microscope. The effect of AM1241 on cell activity and bone tissue differentiation was tested. The SD rat model of cranial bone defect was established, and the defect was repaired by injecting the prepared hydrogel into the defect. The defect was divided into four groups, namely, sham group, blank group, PEG-DTT group, and PEG-DTT + AM1241 group. The rats were euthanized, and whole cranial bone was taken out for micro-CT and histological observation. The prepared hydrogel is porous; it is liquid when heated to 80°C and a hydrogel when cooled to 25°C. 5-10 μM AM1241 increased osteoblast activity. A moderate amount of AM1241 can promote osteogenic differentiation. Both the PEG-DTT group and PEG-DTT + AM1241 group showed obvious new bone tissue formation, but the PEG-DTT + AM1241 group had a better effect. In addition, the new bone tissue in the PEG-DTT + AM1241 group was significantly more than that in the other groups. The prepared AM1241-loaded PEG-DTT hydrogel showed a good repair effect on SD rats with cranial bone defects. It can be used as materials for cranial bone repair in SD rats with cranial bone defects, but the repair effect is weaker than that of normal bone. These results provide a theoretical and practical basis for its further clinical application.

Citing Articles

AM1241 inhibits chondrocyte inflammation and ECM degradation through the Nrf2/HO-1 and NF-κB pathways and alleviates osteoarthritis in mice.

Zou Z, Pan S, Sun C, Wei J, Xu Y, Xiao K Mol Med. 2025; 31(1):9.

PMID: 39794700 PMC: 11721480. DOI: 10.1186/s10020-024-01012-5.


Functional Hydrogels and Their Applications in Craniomaxillofacial Bone Regeneration.

Yu Y, Yu T, Wang X, Liu D Pharmaceutics. 2023; 15(1).

PMID: 36678779 PMC: 9864650. DOI: 10.3390/pharmaceutics15010150.

References
1.
Liu H, Shi X, Wu D, Kahsay Khshen F, Deng L, Dong A . Injectable, Biodegradable, Thermosensitive Nanoparticles-Aggregated Hydrogel with Tumor-Specific Targeting, Penetration, and Release for Efficient Postsurgical Prevention of Tumor Recurrence. ACS Appl Mater Interfaces. 2019; 11(22):19700-19711. DOI: 10.1021/acsami.9b01987. View

2.
Lavanya K, Chandran S, Balagangadharan K, Selvamurugan N . Temperature- and pH-responsive chitosan-based injectable hydrogels for bone tissue engineering. Mater Sci Eng C Mater Biol Appl. 2020; 111:110862. DOI: 10.1016/j.msec.2020.110862. View

3.
Kim Y, Furuya H, Tabata Y . Enhancement of bone regeneration by dual release of a macrophage recruitment agent and platelet-rich plasma from gelatin hydrogels. Biomaterials. 2013; 35(1):214-24. DOI: 10.1016/j.biomaterials.2013.09.103. View

4.
Hojnik M, Dobovisek L, Knez Z, Ferk P . A synergistic interaction of 17-β-estradiol with specific cannabinoid receptor type 2 antagonist/inverse agonist on proliferation activity in primary human osteoblasts. Biomed Rep. 2015; 3(4):554-558. PMC: 4487012. DOI: 10.3892/br.2015.469. View

5.
Zhang J, Shi H, Zhang N, Hu L, Jing W, Pan J . Interleukin-4-loaded hydrogel scaffold regulates macrophages polarization to promote bone mesenchymal stem cells osteogenic differentiation via TGF-β1/Smad pathway for repair of bone defect. Cell Prolif. 2020; 53(10):e12907. PMC: 7574882. DOI: 10.1111/cpr.12907. View