4.7 Article

Multifunctional 3D-Printed Magnetic Polycaprolactone/Hydroxyapatite Scaffolds for Bone Tissue Engineering

Journal

POLYMERS
Volume 13, Issue 21, Pages -

Publisher

MDPI
DOI: 10.3390/polym13213825

Keywords

polycaprolactone; hydroxyapatite scaffolds; 3D additive manufacturing; superparamagnetic nanoparticles; nanocomposites; tissue engineering

Funding

  1. POR-FESR Emilia-Romagna, Italia Custom Implants-Progettazione e Realizzazione di tessuti ed endoprotesi su misura mediante tecnologie sottrattive ed additive [PG/2015/726346]
  2. Italian Ministry of Health
  3. H2020-ICT project [MADIA-732678]

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The study developed magnetically assisted PCL-HAp-1% SPION scaffolds, showing promising results in terms of cell proliferation and osteogenic potential, indicating the potential for further in vitro and in vivo studies and validations.
Multifunctional and resistant 3D structures represent a great promise and a great challenge in bone tissue engineering. This study addresses this problem by employing polycaprolactone (PCL)-based scaffolds added with hydroxyapatite (HAp) and superparamagnetic iron oxide nanoparticles (SPION), able to drive on demand the necessary cells and other bioagents for a high healing efficiency. PCL-HAp-SPION scaffolds with different concentrations of the superparamagnetic component were developed through the 3D-printing technology and the specific topographical features were detected by Atomic Force and Magnetic Force Microscopy (AFM-MFM). AFM-MFM measurements confirmed a homogenous distribution of HAp and SPION throughout the surface. The magnetically assisted seeding of cells in the scaffold resulted most efficient for the 1% SPION concentration, providing good cell entrapment and adhesion rates. Mesenchymal Stromal Cells (MSCs) seeded onto PCL-HAp-1% SPION showed a good cell proliferation and intrinsic osteogenic potential, indicating no toxic effects of the employed scaffold materials. The performed characterizations and the collected set of data point on the inherent osteogenic potential of the newly developed PCL-HAp-1% SPION scaffolds, endorsing them towards next steps of in vitro and in vivo studies and validations.

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