New developments in 3D liquid crystal elastomers scaffolds for tissue engineering: from physical template to responsive substrate

We report here on cell growth and proliferation within a 3D architecture created using smectic liquid crystal elastomers (LCEs) leading to a responsive scaffold for tissue engineering. The investigated LCE scaffolds exhibit biocompatibility, controlled degradability, with mechanical properties and morphologies that can match development of the extracellular matrix. Moreover, the synthetic pathway and scaffold design offer a versatility of processing, allowing modifications of the surface such as adjusting the hydrophilic/hydrophobic balance and the mobility of the LC moieties to enhance the biomaterial performance. First, we succeeded in generating LCEs whose mechanical properties mimic muscle tissue. In films, our LCEs showed cell adhesion, proliferation, and alignment. We also achieved creating 3D LCE structures using either metallic template or microsphere scaffolds. Finally, we recorded a four times higher cell proliferation capability in comparison to conventional porous films and, most importantly, anisotropic cell growth that highlights the tremendous effect of liquid crystal moieties within LCEs on the cell environment.

[1]  Tanmay Bera,et al.  Liquid Crystal Elastomer Microspheres as Three-Dimensional Cell Scaffolds Supporting the Attachment and Proliferation of Myoblasts. , 2015, ACS applied materials & interfaces.

[2]  Michelle T. Leslie,et al.  Effects of Structural Variations on the Cellular Response and Mechanical Properties of Biocompatible, Biodegradable, and Porous Smectic Liquid Crystal Elastomers. , 2017, Macromolecular bioscience.

[3]  Christopher J Murphy,et al.  Indentation versus tensile measurements of Young's modulus for soft biological tissues. , 2011, Tissue engineering. Part B, Reviews.

[4]  T. Maekawa,et al.  POLYMERIC SCAFFOLDS IN TISSUE ENGINEERING APPLICATION: A REVIEW , 2011 .

[5]  T. Sakai Experimental verification of homogeneity in polymer gels , 2014 .

[6]  P. Gennes A semi-fast artificial muscle , 1997 .

[7]  B. Amsden,et al.  Synthesis, characterization and in vitro degradation of a biodegradable elastomer. , 2004, Biomaterials.

[8]  R. Clements,et al.  Biocompatible, biodegradable and porous liquid crystal elastomer scaffolds for spatial cell cultures. , 2015, Macromolecular bioscience.

[9]  D. J. Broer,et al.  Formation of Optical Films by Photo-Polymerisation of Liquid Crystalline Acrylates and Application of These Films in Liquid Crystal Display Technology , 2005 .

[10]  Hsin-I Chang,et al.  Cell Responses to Surface and Architecture of Tissue Engineering Scaffolds , 2011 .

[11]  K. Harris,et al.  Large amplitude light-induced motion in high elastic modulus polymer actuators , 2005 .

[12]  B. Amsden Curable, biodegradable elastomers: emerging biomaterials for drug delivery and tissue engineering. , 2007, Soft matter.

[13]  R. Clements,et al.  Biocompatible 3D Liquid Crystal Elastomer Cell Scaffolds and Foams with Primary and Secondary Porous Architecture. , 2016, ACS macro letters.

[14]  R. Clements,et al.  Role of Surfactant during Microemulsion Photopolymerization for the Creation of Three-Dimensional Liquid Crystal Elastomer Microsphere Spatial Cell Scaffolds , 2016, Front. Mater..

[15]  C. Berkland,et al.  PLG Microsphere Size Controls Drug Release Rate Through Several Competing Factors , 2003, Pharmaceutical Research.

[16]  M. Huneault,et al.  Preparation of interconnected poly(ε-caprolactone) porous scaffolds by a combination of polymer and salt particulate leaching , 2006 .