Biocomposite microfibrous/hydrogel scaffold containing sulfated alginate hydrogel for acceleration of chondrogenic differentiation

• A bio-composite microfibrous/hydrogel scaffold based on surface modified microfibers and sulfated alginate hydrogel was prepared. • PCL microfibers were prepared through centrifugal spinning and were chemically surface-modified with alginate sulfate. • Different binders including sulfated alginate (AS), gelatin (GL), and their combination (AS/GL) were optimized. • Prepared composite scaffold with AS/GL binder imparted the highest compressive modulus. • The expression of cartilage-related genes was higher in composite scaffold with AS/GL binder. In the present research, a fiber/hydrogel biocomposite scaffold consisting of alginate sulfate-modified polycaprolactone fibers and alginate sulfate/gelatin hydrogel was fabricated and its potential as a cartilage scaffold was evaluated. PCL fibers were prepared using centrifugal spinning and functionalized with alginate sulfate chains. Then, to integrate the fibers and construct the composite scaffold, these fibers were mixed with different hydrogel binders including alginate sulfate, gelatin and a combination of both. The analyses performed on the composite scaffolds showed that the porosity of the scaffolds was above 90 %, and their swelling was above 700 %. The compressive modulus of the scaffolds in the dry and wet states was in the range of 16–70 and 4–8 kPa, respectively. In the wet state, the compressive modulus of the scaffold with AS/GL binder increased by 133 and 11 % compared to the scaffolds with AS and GL, respectively. According to cell culture studies, the cell viability of the scaffolds was above 80 %, corroborating their nontoxic nature. In addition, cell adhesion and migration were higher in the scaffolds with GL and AS/GL binders than in the scaffold with AS binder. The expression of cartilage related genes, namely SOX9, COLL II and AGG, in the scaffold with AS/GL binder was 1.4, 3.3 and 4.6 times that of the scaffold with AS binder and 4.8, 8.2 and 8.2 times that of the scaffold with GL binder, respectively. The scaffold with AS/GL binder has great potential for cartilage regeneration by having a higher compressive modulus and providing better chondrogenic differentiation.

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Publication Details

Journal
Materials & Design
Published
2025-06-17
DOI
https://doi.org/10.1016/j.matdes.2025.114259
Citations
1
Primary Topic
Hydrogels: synthesis, properties, applications
Type
article
Field-Weighted Citation Impact
0.59
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article

Biocomposite microfibrous/hydrogel scaffold containing sulfated alginate hydrogel for acceleration of chondrogenic differentiation

Seyed Mohammad Amin Haramshahi, Mohamad Pezeshki‐Modaress, Mahdi Saeed, Nafiseh Bahrami et al.
1 citations
Materials & Design
Hydrogels: synthesis, properties, applications
0.59
article

Biocomposite microfibrous/hydrogel scaffold containing sulfated alginate hydrogel for acceleration of chondrogenic differentiation

Seyed Mohammad Amin Haramshahi, Mohamad Pezeshki‐Modaress, Mahdi Saeed, Nafiseh Bahrami, Seyed Amirhesam Jamali
article en
1 citations

Abstract

• A bio-composite microfibrous/hydrogel scaffold based on surface modified microfibers and sulfated alginate hydrogel was prepared. • PCL microfibers were prepared through centrifugal spinning and were chemically surface-modified with alginate sulfate. • Different binders including sulfated alginate (AS), gelatin (GL), and their combination (AS/GL) were optimized. • Prepared composite scaffold with AS/GL binder imparted the highest compressive modulus. • The expression of cartilage-related genes was higher in composite scaffold with AS/GL binder. In the present research, a fiber/hydrogel biocomposite scaffold consisting of alginate sulfate-modified polycaprolactone fibers and alginate sulfate/gelatin hydrogel was fabricated and its potential as a cartilage scaffold was evaluated. PCL fibers were prepared using centrifugal spinning and functionalized with alginate sulfate chains. Then, to integrate the fibers and construct the composite scaffold, these fibers were mixed with different hydrogel binders including alginate sulfate, gelatin and a combination of both. The analyses performed on the composite scaffolds showed that the porosity of the scaffolds was above 90 %, and their swelling was above 700 %. The compressive modulus of the scaffolds in the dry and wet states was in the range of 16–70 and 4–8 kPa, respectively. In the wet state, the compressive modulus of the scaffold with AS/GL binder increased by 133 and 11 % compared to the scaffolds with AS and GL, respectively. According to cell culture studies, the cell viability of the scaffolds was above 80 %, corroborating their nontoxic nature. In addition, cell adhesion and migration were higher in the scaffolds with GL and AS/GL binders than in the scaffold with AS binder. The expression of cartilage related genes, namely SOX9, COLL II and AGG, in the scaffold with AS/GL binder was 1.4, 3.3 and 4.6 times that of the scaffold with AS binder and 4.8, 8.2 and 8.2 times that of the scaffold with GL binder, respectively. The scaffold with AS/GL binder has great potential for cartilage regeneration by having a higher compressive modulus and providing better chondrogenic differentiation.

Materials & DesignVol. 256
Iran University of Medical Sciences (IR), Islamic Azad University Central Tehran Branch (IR)
Openalex Percentile: Top 35%
Hydrogels: synthesis, properties, applications
0.59
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