Stretchable hydrogels of chitosan/hyaluronic acid induced by polyelectrolyte complexation around neutral pH

被引:9
作者
Balima, Maeva [1 ]
Morfin, Isabelle [2 ]
Sudre, Guillaume [1 ]
Montembault, Alexandra [1 ]
机构
[1] Univ Jean Monnet, Univ Claude Bernard Lyon 1, INSA Lyon,Ingenierie Materiaux Polymeres, CNRS,UMR 5223, F-69622 Villeurbanne, France
[2] Univ Grenoble Alpes, CNRS, LiPhy, F-38000 Grenoble, France
关键词
Chitosan; Hyaluronic acid; Stretchable hydrogels; Physical crosslinking; Polyelectrolyte complexation; Metal complexation; HYALURONIC-ACID; CHITOSAN HYDROGELS; CROSS-LINKING; SUPRAMOLECULAR HYDROGELS; NETWORK HYDROGELS; AQUEOUS-SOLUTION; CHITIN; NANOPARTICLES; COACERVATION; STRENGTH;
D O I
10.1016/j.carbpol.2024.122265
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In this work, we propose the formation of stretchable hydrogels at neutral pH from the physical crosslinking of chitosan (CS) and hyaluronic acid (HA) by polyelectrolyte complexation. A mixture of CS (Mw approximate to 600 kg/mol, degree of acetylation approximate to 50 %) solution and HA (Mw approximate to 77 kg/mol) solution was prepared with an excess of salts screening the electrostatic interactions CS/HA. In a controlled manner, the polyelectrolyte complexation was induced through the progressive dialysis of the salted polymer mixture against a sodium acetate solution (AcONa, 0.01 M) for 7 days. Depending on [HA], various materials were obtained: viscous solutions at [HA] = 0.75 % (w/v); hydrogels at [HA] = 1.50-2.24 % (w/v) with Young modulus of 14 kPa and stretchable to 200 %. The small angle X-ray scattering characterization of the hydrogels revealed a multiscale organization related to the conformation of the polymers induced by the physical interactions. The dialysis process with AcONa was optimized by adding a dialysis step against a zinc acetate solution containing Zn2+. The combination of polyelectrolyte complexation between CS/HA and metal complexation between Zn2+ and the polymers led to an enhancement of the hydrogel stretchability up to 400 %.
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页数:12
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