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Modelling methacrylated chitosan hydrogel properties through an experimental design approach: from composition to material properties

自愈水凝胶 壳聚糖 材料科学 化学工程 作文(语言) 复合材料 高分子科学 高分子化学 哲学 语言学 工程类
作者
Alessio Bucciarelli,Nora Selicato,Chiara Coricciati,Alberto Rainer,Agostina Lina Capodilupo,Giuseppe Gigli,Lorenzo Moroni,Alessandro Polini,Francesca Gervaso
出处
期刊:Journal of Materials Chemistry B [Royal Society of Chemistry]
卷期号:12 (40): 10221-10240 被引量:13
标识
DOI:10.1039/d4tb00670d
摘要

Hydrogels of biopolymers are gradually substituting synthetic hydrogels in tissue engineering applications due to their properties. However, biopolymeric hydrogels are difficult to standardize because of the intrinsic variability of the material and the reversibility of physical crosslinking processes. In this work, we synthesized a photocrosslinkable derivative of chitosan (Cs), namely methacrylated chitosan (CsMA), in which the added methacrylic groups allow the formation of hydrogels through radical polymerization triggered by UV exposure. We then performed a systematic study to link the physical properties of the materials to its preparation parameters to standardize its preparation according to specific applications. We studied the properties of CsMA solutions and the derived hydrogels using a statistical method, namely, response surface method, which allowed us to build empirical models describing material properties in terms of several selected processing factors. In particular, we studied the viscosity of CsMA solutions as a function of CsMA concentration, temperature, and shear rate, while hydrogel compression modulus, morphology, degradation and solubilization were investigated as a function of CsMA concentration, photoinitiator concentration and UV exposure. CsMA solutions resulted in shear thinning and were thus suitable for extrusion-based 3D printing. The CsMA hydrogel was found to be highly tunable, with a stiffness in the 12-64 kPa range, and was stable over a long timeframe (up to 60 days). Finally, the possibility to engineer hydrogel stiffness through an empirical model allowed us to hypothesize a number of possible applications based on the mechanical properties of several biological tissues reported in the literature.
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