3.8 Article

Mechanical Integrity in a Dynamic Interpenetrating Hydrogel Network of Supramolecular Peptide-Polysaccharide Supports Enhanced Chondrogenesis

期刊

ACS BIOMATERIALS SCIENCE & ENGINEERING
卷 7, 期 12, 页码 5798-5809

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsbiomaterials.1c01120

关键词

supramolecular peptide; double-network hydrogel; polysaccharide; chondrocytes; cartilage tissue engineering

资金

  1. Department of Biotechnology, India [BT/PR22067/NNT/28/1163/2016]
  2. Department of Science and Technology, India [SERB/F/755/2019-2020, CRG/2020/004251]

向作者/读者索取更多资源

Tissue engineering requires scaffolds with properties similar to target tissues, such as mechanical and bioactive properties. A unique hydrogel scaffold has been developed using a dynamic interpenetrating network to support chondrocyte growth and differentiation, providing favorable 3D microarchitecture and optimal mechanical characteristics essential for cartilage tissue engineering. The hydrogel's adaptable nature and dynamic interactions play a crucial role in influencing structure and mechanical properties, demonstrating potential for supporting in vitro chondrogenesis and cartilage tissue regeneration.
Tissue engineering demands intelligently designed scaffolds that encompass the properties of the target tissues in terms of mechanical and bioactive properties. An ideal scaffold for engineering a cartilage tissue should provide the chondrocytes with a favorable 3D microarchitecture apart from possessing optimal mechanical characteristics such as compressibility, energy dissipation, strain stiffening, etc. Herein, we used a unique design approach to develop a hydrogel having a dynamic interpenetrating network to serve as a framework to support chondrocyte growth and differentiation. An amyloid-inspired peptide amphiphile (1) was self-assembled to furnish kinetically controlled nanofibers and incorporated in a dynamic covalently cross-linked polysaccharide network of carboxymethyl cellulose dialdehyde (CMC-D) and carboxymethyl chitosan (CMCh) using Schiff base chemistry. The dynamic noncovalent interaction played a pivotal role in providing the desired modulation in the structure and mechanical properties of the double-network hydrogels that are imperative for cartilage scaffold design. The adaptable nature supported shear-induced extrusion of the hydrogel and facilitated various cellular functions while maintaining its integrity. The potential of the as-developed hydrogels to support in vitro chondrogenesis was explored using human chondrocytes. Evidence of improved cell growth and cartilage-specific ECM production confirmed the potential of the hydrogel to support cartilage tissue engineering while reaffirming the significance of mimicking the biophysical microenvironment to induce optimal tissue regeneration.

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