Martinez-Vazquez_2013_J.Biomed.Mater.Res.A_101_3086

Reference

Title : Impregnation of beta-tricalcium phosphate robocast scaffolds by in situ polymerization - Martinez-Vazquez_2013_J.Biomed.Mater.Res.A_101_3086
Author(s) : Martinez-Vazquez FJ , Perera FH , van der Meulen I , Heise A , Pajares A , Miranda P
Ref : J Biomed Mater Res A , 101 :3086 , 2013
Abstract :

Ring-opening polymerization of sigma-caprolactone (sigma-CL) and L-lactide (LLA) was performed to impregnate beta-tricalcium phosphate (beta-TCP) scaffolds fabricated by robocasting. Concentrated colloidal inks prepared from beta-TCP commercial powders were used to fabricate porous structures consisting of a 3D mesh of interpenetrating rods. sigma-CL and LLA were in situ polymerized within the ceramic structure by using a lipase and stannous octanoate, respectively, as catalysts. The results show that both the macropores inside the ceramic mesh and the micropores within the ceramic rods are full of polymer in either case. The mechanical properties of scaffolds impregnated by in situ polymerization (ISP) are significantly increased over those of the bare structures, exhibiting similar values than those obtained by other, more aggressive, impregnation methods such as melt-immersion (MI). ISP using enzymatic catalysts requires a reduced processing temperature which could facilitate the incorporation of growth factors and other drugs into the polymer composition, thus enhancing the bioactivity of the composite scaffold. The implications of these results for the optimization of the mechanical and biological performance of scaffolds for bone tissue engineering applications are discussed.

PubMedSearch : Martinez-Vazquez_2013_J.Biomed.Mater.Res.A_101_3086
PubMedID: 23526780

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Citations formats

Martinez-Vazquez FJ, Perera FH, van der Meulen I, Heise A, Pajares A, Miranda P (2013)
Impregnation of beta-tricalcium phosphate robocast scaffolds by in situ polymerization
J Biomed Mater Res A 101 :3086

Martinez-Vazquez FJ, Perera FH, van der Meulen I, Heise A, Pajares A, Miranda P (2013)
J Biomed Mater Res A 101 :3086