Abstract

Efforts to develop versatile tissue-engineered scaffolds mimicking the functions of extracellular matrices (ECMs) have led to the emergence of liquid crystalline elastomers (LCEs) as promising materials. Here, thiol-acrylate-based LCEs forming a nematic phase upon UV irradiation were synthesized, and their biological compatibility was evaluated using C2C12 myoblast cells. Prior to UV exposure, some characteristics, e.g., phase transition temperature (TNI), order parameter, and reaction time, of the as-synthesized LCEs are characterized for property optimization. Fourier-transform infrared spectroscopy revealed that thiol-acrylate Michael addition polymerization was successful, judged by the disappearance of the characteristic peaks of thiol and acrylate groups. Differential scanning calorimetry thermograms and dynamic mechanical thermal analysis curves showed TNI values at ca. 49 °C, at which point the nematic phase is the dominant morphology. Moreover, the cross-linking density, the fixing, and the recovery ratios for the sample with optimal properties (i.e., LCE3) were determined to be 10.3 mol/cm3, 97.2 % and 91 %, respectively. Assessment of mesomorphism and roughness demonstrated the suitability of LCE3 for cell culture. Subsequent studies on adhesion, viability, differentiation, and proliferation of cultured myoblast cells, coupled with particle image velocimetry simulation, highlighted the potential of UV-irradiated LCE3 as a promising scaffold material for inducing surface morphology-induced cellular alignment and interactions.

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