Cytotoxicity and Degradation Resistance of Cryo- and Hydrogels Based on Carboxyethylchitosan at Different pH Values

• Published in: Gels 2024-04, Vol.10 (4), p.272
• Main Authors: Blinova, Elena, Korel, Anastasia, Zemlyakova, Ekaterina, Pestov, Alexander, Samokhin, Alexander, Zelikman, Maxim, Tkachenko, Vadim, Bets, Viktoria, Arzhanova, Elena, Litvinova, Ekaterina
• Format: Article
• Language: English
• Subjects: Analysis; Aqueous solutions; carboxyethylchitosan; Chitosan; crosslink ratio; Crosslinked polymers; Crosslinking; cryogel; Cytotoxicity; Degradation; Equilibrium; Fibroblasts; Flow cytometry; Glutaraldehyde; hydrogel; Hydrogels; Hydrogen-ion concentration; Hypotheses; Medical research; Optical microscopy; Statistical analysis; Swelling; Synthesis; Toxicity testing
• ISSN: 2310-2861; 2310-2861
• DOI: 10.3390/gels10040272

The use of chitosan-based gels is still limited due to their restricted solubility in acid solutions, where the molecules have a positive charge. The functionalization of chitosan makes it possible to significantly expand the possibilities of using both the polymer itself and hydrogels based on its derivatives. To evaluate the effect of the conditions for the production of cryo- and hydrogels based on carboxyethylchitosan (CEC) crosslinked with glutaraldehyde on gel swelling and its resistance to degradation depending on pH and cytotoxic effects and to test the hypothesis that the amount of crosslinking agent during synthesis may affect the cytotoxicity of the gel. Gels' swelling values and degradation resistance were determined using the gravimetric method. The cytotoxic effect was evaluated during the co-cultivation of gels in the presence of human fibroblasts using light optical microscopy and flow cytometry. All CEC-based cryogels had a higher equilibrium swelling value and degradation time than the CEC hydrogel in the pH range from 4.6 to 8.0. This demonstrates the superiority of cryogels relative to CEC-based hydrogels in terms of swelling potential and degradation resistance, while an increase in the number of crosslinks with glutaraldehyde contributes to longer swelling of the cryogel. The positive control (intact fibroblasts) and all gel samples were statistically identical in the number of viable cells. On the third day, the viability of the fibroblast cells was consistently high (above 95%) and did not differ between all tested CEC-based gels. And in general, the cell morphology analysis results corresponded with the results obtained in the flow cytometry-based cytotoxicity test. We also did not find proof in our experiment to support our hypothesis that the amount of crosslinking agent during synthesis may affect the cytotoxicity of the material.