3D printed PCL/nHAp scaffolds: Influence of scaffold structural parameters on osteoblast performance in vitro

Author:

Yazdanpanah Zahra1,Ketabat Farinaz1,Gomez‐Picos Patsy2,Raquin Alice13,Fazel Anvari‐Yazdi Abbas1ORCID,Eames B. Frank12,Johnston James D.14,Cooper David M. L.2,Chen Xiongbiao14ORCID

Affiliation:

1. Division of Biomedical Engineering College of Engineering University of Saskatchewan Saskatoon Saskatchewan Canada

2. Department of Anatomy, Physiology, and Pharmacology College of Medicine University of Saskatchewan Saskatoon Saskatchewan Canada

3. Institut Catholique des Arts et Métiers La Roche‐sur‐Yon France

4. Department of Mechanical Engineering College of Engineering University of Saskatchewan Saskatoon Saskatchewan Canada

Abstract

AbstractScaffolds play a key role in bone tissue engineering (BTE) as they provide a mechanically and biologically supportive template to treat bone defects. Yet, the ideal scaffold structures are far from certain, leaving a lot to be discovered in terms of the scaffold structure–performance relationships. In this study, we investigated the influence of pore size and internal structure on osteoblast performance in vitro. Three‐dimensional (3D) scaffolds were printed from polycaprolactone (PCL) reinforced with 30% (wt.) nano‐hydroxyapatite (nHAp), with two different internal structures (lattice and staggered) and four pore sizes (0.280, 0.380, 0.420, and 0.550 mm). Scaffolds were seeded with pre‐osteoblast cells (MC3T3‐E1). Metabolic activity of cells, osteoblast differentiation, and capability of osteoblasts to deposit mineralized matrix were examined in vitro. Staggered scaffolds better supported cellular performance. The pore size of 0.280 mm was more favorable to support cell proliferation while the pore size ≥0.420 mm was more effective to promote osteoblast differentiation and mineralization. Findings revealed that osteoblast activities were affected differently by the pore size. Our study further suggests that the structure with a gradient pore size would be better than a single size in terms of supporting cell proliferation, differentiation, and secretion of a mineralized matrix.

Funder

University of Saskatchewan

Saskatchewan Health Research Foundation

Publisher

Wiley

Subject

Industrial and Manufacturing Engineering

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