Document Type
Article
Publication Date
2025
DOI
10.1016/j.carpta.2025.100696
Publication Title
Carbohydrate Polymer Technologies and Applications
Volume
9
Pages
100696 (1-16)
Abstract
Osteoarthritis is a leading cause of disability worldwide, challenging current treatments to limited cartilage self-healing capacity. Cartilage tissue engineering (CTE) integrates cells, scaffolds, and signaling molecules, with Insulin being utilized as a differentiation biomolecule due to cost-effectiveness, dose-dependent influence on chondrogenesis, suitable biological activity, and ability to activate relevant receptors. Yet, administering differentiation biomolecules through conventional scaffolds poses a persistent challenge. Alginate (Alg) is commonly employed in CTE for its biocompatibility, though it lacks sufficient mechanical properties. Chitosan (Cs), while enhancing scaffold mechanical properties, but does not independently provide optimal support for chondrogenesis. While Alg-Cs scaffolds have garnered attention, challenges persist in achieving sustained differentiation biomolecules delivery and attaining suboptimal structural and biological properties for cartilage regeneration. This study utilizes advanced scaffolds by employing three dimensional (3D) printing technique to create Insulin-loaded Alg-Cs scaffolds, examining their structural, mechanical, and release properties, and assessing cell viability and chondrogenic differentiation through markers like COL1A1, COL2A1, SOX9 and ACAN. Following a 30-day implantation period, we also evaluate histological parameters. The findings revealed that the incorporation of a 20 (μg/ml) dose of Insulin into Alg-Cs 3D-printed scaffolds significantly enhanced the expression of these markers, indicating improved chondrogenic potential for cartilage regeneration. Histological analysis confirmed favorable biocompatibility and structural integrity of Insulin-loaded pure Alg and Alg-Cs scaffolds at drug loading levels of up to 20 and 10 μg, respectively. The hypothesis suggests that these advanced scaffolds can achieve controlled Insulin release, enhancing cartilage regeneration. This research aims to develop to yield mechanically optimized, bioactive 3D-printed scaffolds for regulated delivery of Insulin to promote cartilage regeneration.
Rights
© 2025 The Authors.
This is an open access article under the Creative Commons Attribution 4.0 International (CC BY 4.0) License.
Data Availability
Article states: "Data will be made available on request."
Original Publication Citation
Jahani, A., Nourbakhsh, M. S., Moradi, A., Mohammadi, M., & Tayebi, L. (2025). Incorporating insulin into alginate-chitosan 3D-printed scaffolds: A comprehensive study on structure, mechanics, and biocompatibility for cartilage tissue engineering. Carbohydrate Polymer Technologies and Applications, 9, 1-16, Article 100696. https://doi.org/10.1016/j.carpta.2025.100696
Repository Citation
Jahani, Afsaneh; Nourbakhsh, Mohammad Sagdegh; Moradi, Ali; Mohammadi, Marzieh; and Tayebi, Lobat, "Incorporating Insulin Into Alginate-Chitosan 3D-Printed Scaffolds: A Comprehensive Study on Structure, Mechanics, and Biocompatibility for Cartilage Tissue Engineering" (2025). Electrical & Computer Engineering Faculty Publications. 509.
https://digitalcommons.odu.edu/ece_fac_pubs/509
Included in
Molecular, Cellular, and Tissue Engineering Commons, Musculoskeletal Diseases Commons, Polymer Science Commons, Rheumatology Commons
