Bone tissue engineering has developed significantly in recent years as there has been increasing demand for bone substitutes due to trauma, cancer, arthritis, and infections. The scaffolds for bone regeneration need to be mechanically stable and have a 3D architecture with intercon-nected pores. With the advances in additive manufacturing technology, these requirements can be fulfilled by 3D printing scaffolds with controlled geometry and porosity using a low‐cost multistep process. The scaffolds, however, must also be bioactive to promote the environment for the cells to regenerate into bone tissue. To determine if a low‐cost 3D printing method for bespoke SiOC(N) porous structures can regenerate bone, these structures were tested for osteointegration potential by using human mesenchymal stem cells (hMSCs). This includes checking the general biocompati-bilities under the osteogenic differentiation environment (cell proliferation and metabolism). Moreover, cell morphology was observed by confocal microscopy, and gene expressions on typical osteogenic markers at different stages for bone formation were determined by real‐time PCR. The results of the study showed the pore size of the scaffolds had a significant impact on differentiation. A certain range of pore size could stimulate osteogenic differentiation, thus promoting bone regrowth and regeneration.

3d printed sioc(N) ceramic scaffolds for bone tissue regeneration: Improved osteogenic differentiation of human bone marrow‐derived mesenchymal stem cells / Yang, Yuejiao; Kulkarni, Apoorv; Sorarù, Gian Domenico; Pearce, Joshua M.; Motta, Antonella. - In: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. - ISSN 1661-6596. - ELETTRONICO. - 22:24(2021), pp. 13676.1-13676.14. [10.3390/ijms222413676]

3d printed sioc(N) ceramic scaffolds for bone tissue regeneration: Improved osteogenic differentiation of human bone marrow‐derived mesenchymal stem cells

Yang, Yuejiao;Kulkarni, Apoorv;Sorarù, Gian Domenico;Motta, Antonella
2021-01-01

Abstract

Bone tissue engineering has developed significantly in recent years as there has been increasing demand for bone substitutes due to trauma, cancer, arthritis, and infections. The scaffolds for bone regeneration need to be mechanically stable and have a 3D architecture with intercon-nected pores. With the advances in additive manufacturing technology, these requirements can be fulfilled by 3D printing scaffolds with controlled geometry and porosity using a low‐cost multistep process. The scaffolds, however, must also be bioactive to promote the environment for the cells to regenerate into bone tissue. To determine if a low‐cost 3D printing method for bespoke SiOC(N) porous structures can regenerate bone, these structures were tested for osteointegration potential by using human mesenchymal stem cells (hMSCs). This includes checking the general biocompati-bilities under the osteogenic differentiation environment (cell proliferation and metabolism). Moreover, cell morphology was observed by confocal microscopy, and gene expressions on typical osteogenic markers at different stages for bone formation were determined by real‐time PCR. The results of the study showed the pore size of the scaffolds had a significant impact on differentiation. A certain range of pore size could stimulate osteogenic differentiation, thus promoting bone regrowth and regeneration.
2021
24
Yang, Yuejiao; Kulkarni, Apoorv; Sorarù, Gian Domenico; Pearce, Joshua M.; Motta, Antonella
3d printed sioc(N) ceramic scaffolds for bone tissue regeneration: Improved osteogenic differentiation of human bone marrow‐derived mesenchymal stem cells / Yang, Yuejiao; Kulkarni, Apoorv; Sorarù, Gian Domenico; Pearce, Joshua M.; Motta, Antonella. - In: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. - ISSN 1661-6596. - ELETTRONICO. - 22:24(2021), pp. 13676.1-13676.14. [10.3390/ijms222413676]
File in questo prodotto:
File Dimensione Formato  
yang-ijms-22-13676-v2.pdf

accesso aperto

Tipologia: Versione editoriale (Publisher’s layout)
Licenza: Creative commons
Dimensione 3.4 MB
Formato Adobe PDF
3.4 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11572/355762
Citazioni
  • ???jsp.display-item.citation.pmc??? 3
  • Scopus 10
  • ???jsp.display-item.citation.isi??? 9
social impact