4.8 Article

Pore Size of 3D-Printed Polycaprolactone/Polyethylene Glycol/Hydroxyapatite Scaffolds Affects Bone Regeneration by Modulating Macrophage Polarization and the Foreign Body Response

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 14, Issue 18, Pages 20693-20707

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c02001

Keywords

3D-printed scaffold; pore size; macrophage polarization; foreign body response; bone regeneration

Funding

  1. National Natural Science Foundation of China [82060203, 31960207]
  2. Key Project of Jiangxi Education Department [GJJ180010]

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This study investigates the effect of pore size of 3D-printed scaffolds on immune response and bone-biomaterial integration. It was found that larger pore sizes can significantly reduce foreign body response and promote macrophage infiltration, vascular ingrowth, and new bone formation, thus providing better results for bone defect repair.
3D-printed porous bioactive ceramic scaffolds have been widely used in bone defect repair. However, material implantation is often accompanied by a foreign body response (FBR), which may affect host tissue regeneration. The physical properties of biomaterials, including shape, pore size, and porosity, control the relevant immune responses during tissue regeneration. To the best of our knowledge, the effect of the pore size of 3D-printed scaffolds on the immune response and bone-biomaterial integration has not been studied in vivo. Polycaprolactone/polyethylene glycol/hydroxyapatite (PC L/PEG/HA ) bioactive scaffolds with different pore sizes, including 209.9 +/- 77.1 mu m (P200), 385.5 +/- 28.6 mu m (P400), and 582.1 +/- 27.2 mu m (P600), were prepared with a pneumatic extrusion 3D printer. Compared with other pore sizes, P600 significantly reduced the FBR and induced more M2 macrophage infiltration, vascular ingrowth, and new bone formation. Immunohistochemical staining revealed that the MyD88 protein might be involved in macrophage polarization-related signal transduction in response to the pore size. Based on these results, bone regeneration requires the active participation of the immune response, and the P600 PCL/PEG/HA scaffold is a preferable candidate for the repair of bone defects.

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