Issue 18, 2024

Injectable hydrogels for bone regeneration with tunable degradability via peptide chirality modification

Abstract

The degradability of hydrogels plays a pivotal role in bone regeneration, yet its precise effects on the bone repair process remain poorly understood. Traditional studies have been limited by the use of hydrogels with insufficient variation in degradation properties for thorough comparative analysis. Addressing this gap, our study introduces the development of matrix metalloproteinase (MMP)-responsive hydrogels engineered with a tunable degradation rate, specifically designed for bone regeneration applications. These innovative hydrogels are synthesized by integrating MMP-sensitive peptides, which exhibit chirality-transferred amino acids, with norbornene (NB)-modified 8-arm polyethylene glycol (PEG) macromers to form the hydrogel network. The degradation behavior of these hydrogels is manipulated through the chirality of the incorporated peptides, resulting in the classification into L, LD, and D hydrogels. Remarkably, the L hydrogel variant shows a significantly enhanced degradation rate, both in vitro and in vivo, which in turn fosters bone regeneration by promoting cell migration and upregulating osteogenic gene expression. This research highlights the fundamental role of hydrogel degradability in bone repair and lays the groundwork for the advancement of degradable hydrogel technologies for bone regeneration, offering new insights and potential for future biomaterials development.

Graphical abstract: Injectable hydrogels for bone regeneration with tunable degradability via peptide chirality modification

Supplementary files

Article information

Article type
Communication
Submitted
07 Apr 2024
Accepted
20 Jun 2024
First published
26 Jun 2024

Mater. Horiz., 2024,11, 4367-4377

Injectable hydrogels for bone regeneration with tunable degradability via peptide chirality modification

W. Chen, S. Sheng, K. Tan, S. Wang, X. Wu, J. Yang, Y. Hu, L. Cao, K. Xu, F. Zhou, J. Su, Q. Zhang and L. Yang, Mater. Horiz., 2024, 11, 4367 DOI: 10.1039/D4MH00398E

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