Laser-direct writing by two-photon polymerization of 3D honeycomb-like structures for bone regeneration

Biofabrication. 2018 Feb 5;10(2):025009. doi: 10.1088/1758-5090/aaa718.

Abstract

A major limitation of existing 3D implantable structures for bone tissue engineering is that most of the cells rapidly attach on the outer edges of the structure, restricting the cells penetration into the inner parts and causing the formation of a necrotic core. Furthermore, these structures generally possess a random spatial arrangement and do not preserve the isotropy on the whole volume. Here, we report on the fabrication and testing of an innovative 3D hierarchical, honeycomb-like structure (HS), with reproducible and isotropic arhitecture, that allows in 'volume' migration of osteoblasts. In particular, we demonstrate the possibility to control the 3D spatial cells growth inside these complex architectures by adjusting the free spaces inside the structures. The structures were made of vertical microtubes arranged in a mulitlayered configuration, fabricated via laser direct writing by two photons polymerization of the IP-L780 photopolymer. In vitro tests performed in MG-63 osteoblast-like cells demonstrated that the cells migration inside the 3D structures is conducted by the separation space between the microtubes layers. Specifically, for layers separation between 2 and 10 μm, the cells gradually penetrated between the microtubes. Furthermore, these structures induced the strongest cells osteogenic differentiation and mineralization, with ALP activity 1.5 times stronger, amount of calcified minerals 1.3 times higher and osteocalcin secretion increased by 2.3 times compared to the other structures. On the opposite, for layers separation less than 2 μm and above 10 μm, the cells were not able to make interconnections and exhibited poor mineralization ability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Regeneration / physiology*
  • Cell Differentiation
  • Cell Line, Tumor
  • Humans
  • Osteoblasts / cytology
  • Osteocalcin / analysis
  • Osteocalcin / metabolism
  • Osteogenesis / physiology*
  • Polymerization
  • Tissue Engineering / methods*
  • Tissue Scaffolds*

Substances

  • Osteocalcin