Abstract

The aim of this work is to evaluate the potential of cryogels to be used as scaffolds in tissue engineering. Scaffolds based on the α-tricalcium phosphate reinforced PDMAEMA (Poly(dimethyl aminoethyl methacrylate))/PHEMA (poly(hydroxyethyl methacrylate)) system were prepared and human trabecular bone-derived cells (HTBs) and bone marrow derived-mesenchymal stem cells (BM-MSCs) cultured on them. Several features, such as porosity, pore shape, molecular weight between crosslinks and mesh size, are studied. The most suitable PDMAEMA/PHEMA ratio for cell proliferation has been assessed and the viability, adhesion, proliferation and expression of osteoblastic biochemical markers are evaluated. The PDMAEMA/PHEMA ratio influences the scaffolds porosity. Values between 53% ± 5.7% for a greater content in PHEMA and 75% ± 5.5% for a greater content in PDMAEMA have been obtained. The polymer ratio also modifies the pore shape. A greater content in PDMAEMA leads also to bigger network mesh size. Each of the compositions were non-cytotoxic, the seeded cells remained viable for both BM-MSCs and HTBs. Thus, and based on the structural analysis, specimens with a greater content in PDMAEMA seem to provide a better structural environment for their use as scaffolds for tissue engineering. The α-tricalcium phosphate incorporation into the composition seems to favor the expression of the osteogenic phenotype.

Highlights

  • Cryogels have considerable potential for applications as scaffolds for tissue engineering since they may provide with the necessary support for cells to proliferate and maintain their differentiated function [1,2]

  • The most suitable ratio of DMAEMA/HEMA and the consequences of introducing α-tricalcium phosphate will be evaluated based on the resulting structural features and on the response of cultured human trabecular bone-derived cells and human mesenchymal stem cells

  • Methacrylate MAEMA/PHEMA reinforced with α-tricalcium phosphate can be prepared by cryopolymerization

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Summary

Introduction

Cryogels have considerable potential for applications as scaffolds for tissue engineering since they may provide with the necessary support for cells to proliferate and maintain their differentiated function [1,2]. Cryotopic gelation is a specific type of gelation that takes place upon cryogenic treatment of initial systems potentially capable of forming a gel [3]. The cryogel structure is mainly controlled by the freezing conditions because the formed solvent crystals acts as the porogenic factor [4]. After melting the solvent crystals, a system of large interconnected pores is formed. The formation of interconnections occurs when ice crystals from the solvent grow enough to connect with another ice crystal [5]. Concomitant with the solvent crystallization, there is an increase in the monomers concentration in the remaining liquid solvent that leads to the polymerization, by a phenomenon called cryoconcentration

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