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Updated: Aug 1, 2026

Simple Polyacrylamide-based Multiwell Stiffness Assay for the Study of Stiffness-dependent Cell Responses
Published on: March 25, 2015
Chitosan/vanillin/polydimethylsiloxane scaffolds with tunable stiffness for muscle cell proliferation
Rafael Leonardo Cruz Gomes da Silva1, Dragica Bezjak2, Tomas P Corrales3
1Fundamental Chemistry Department, Institute of Chemistry, University of São Paulo, Av. Prof. Lineu Prestes 748, 05508-000 São Paulo, Brazil.
This study developed tunable chitosan scaffolds using polydimethylsiloxane (PDMS) for C2C12 myoblasts. Scaffolds showed modulated mechanical properties and good cell adhesion, with chitosan-PDMS exhibiting better viability than vanillin-based ones.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Polymer Chemistry
Background:
- Scaffold mechanical properties critically impact cell behavior.
- Chitosan and vanillin-crosslinked chitosan are promising biomaterials for tissue regeneration.
- Tailoring scaffold mechanics is essential for optimizing cell response.
Purpose of the Study:
- To develop a methodology for producing chitosan and vanillin-crosslinked chitosan films with tunable mechanical properties.
- To investigate the influence of polydimethylsiloxane (PDMS) elastomer incorporation on scaffold mechanics.
- To evaluate the suitability of these scaffolds for C2C12 myoblast applications.
Main Methods:
- Preparation of aqueous PDMS elastomeric dispersions using polysorbate 20.
- Incorporation of PDMS dispersions into chitosan or vanillin-crosslinked chitosan polymeric dispersions.
- Fabrication of films via casting and characterization using atomic force microscopy (AFM) in force spectroscopy mode.
- Assessment of mechanical properties (elastic modulus), swelling degree, gel content, cell viability, and cell adhesion.
Main Results:
- PDMS incorporation successfully modulated the elastic modulus (E) of chitosan scaffolds (60–200 kPa) and vanillin-based scaffolds (200–600 kPa).
- Softer scaffolds exhibited higher swelling and lower gel content.
- Chitosan-PDMS scaffolds showed good cell viability and C2C12 myoblast adhesion across a range of elastic moduli (114–568 kPa).
- Vanillin-based scaffolds displayed borderline cytotoxicity (~70% viability).
Conclusions:
- A novel method for creating tunable mechanical property scaffolds from chitosan and vanillin-crosslinked chitosan was established.
- PDMS elastomer incorporation offers a viable strategy to control scaffold mechanics for tissue engineering applications.
- Chitosan-PDMS scaffolds demonstrate potential for C2C12 myoblast culture due to favorable mechanical properties and biocompatibility.
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