Early In Vivo Osteogenic and Inflammatory Response of 3D Printed Polycaprolactone/Carbon Nanotube/Hydroxyapatite/Tricalcium Phosphate Composite Scaffolds
| dc.contributor.author | Nalesso, Paulo Roberto Lopes | |
| dc.contributor.author | Vedovatto, Matheus | |
| dc.contributor.author | Gregório, Julia Eduarda Schneider | |
| dc.contributor.author | Huang, Boyang | |
| dc.contributor.author | Vyas, Cian | |
| dc.contributor.author | Santamaria-Jr, Milton [UNESP] | |
| dc.contributor.author | Bártolo, Paulo | |
| dc.contributor.author | Caetano, Guilherme Ferreira | |
| dc.contributor.institution | University Centre of Hermínio Ometto Foundation | |
| dc.contributor.institution | Nanyang Technological University | |
| dc.contributor.institution | The University of Manchester | |
| dc.contributor.institution | Universidade Estadual Paulista (UNESP) | |
| dc.contributor.institution | Universidade de São Paulo (USP) | |
| dc.date.accessioned | 2025-04-29T20:09:04Z | |
| dc.date.issued | 2023-07-01 | |
| dc.description.abstract | The development of advanced biomaterials and manufacturing processes to fabricate biologically and mechanically appropriate scaffolds for bone tissue is a significant challenge. Polycaprolactone (PCL) is a biocompatible and degradable polymer used in bone tissue engineering, but it lacks biofunctionalization. Bioceramics, such as hydroxyapatite (HA) and β tricalcium phosphate (β-TCP), which are similar chemically to native bone, can facilitate both osteointegration and osteoinduction whilst improving the biomechanics of a scaffold. Carbon nanotubes (CNTs) display exceptional electrical conductivity and mechanical properties. A major limitation is the understanding of how PCL-based scaffolds containing HA, TCP, and CNTs behave in vivo in a bone regeneration model. The objective of this study was to evaluate the use of three-dimensional (3D) printed PCL-based composite scaffolds containing CNTs, HA, and β-TCP during the initial osteogenic and inflammatory response phase in a critical bone defect rat model. Gene expression related to early osteogenesis, the inflammatory phase, and tissue formation was evaluated using quantitative real-time PCR (RT-qPCR). Tissue formation and mineralization were assessed by histomorphometry. The CNT+HA/TCP group presented higher expression of osteogenic genes after seven days. The CNT+HA and CNT+TCP groups stimulated higher gene expression for tissue formation and mineralization, and pro- and anti-inflammatory genes after 14 and 30 days. Moreover, the CNT+TCP and CNT+HA/TCP groups showed higher gene expressions related to M1 macrophages. The association of CNTs with ceramics at 10wt% (CNT+HA/TCP) showed lower expressions of inflammatory genes and higher osteogenic, presenting a positive impact and balanced cell signaling for early bone formation. The association of CNTs with both ceramics promoted a minor inflammatory response and faster bone tissue formation. | en |
| dc.description.affiliation | Graduate Program in Biomedical Sciences University Centre of Hermínio Ometto Foundation, SP | |
| dc.description.affiliation | Singapore Centre for 3D Printing School of Mechanical and Aerospace Engineering Nanyang Technological University, Jurong West | |
| dc.description.affiliation | School of Mechanical Aerospace and Civil Engineering The University of Manchester | |
| dc.description.affiliation | Graduate Program of Orthodontics University Centre of Hermínio Ometto Foundation, SP | |
| dc.description.affiliation | Department of Social and Pediatric Dentistry UNESP - São Paulo State University Institute of Science and Technology - College of Dentistry, SP | |
| dc.description.affiliation | Division of Dermatology Department of Internal Medicine Ribeirão Preto Medical School São Paulo University (USP), SP | |
| dc.description.affiliationUnesp | Department of Social and Pediatric Dentistry UNESP - São Paulo State University Institute of Science and Technology - College of Dentistry, SP | |
| dc.description.sponsorship | Engineering and Physical Sciences Research Council | |
| dc.identifier | http://dx.doi.org/10.3390/polym15132952 | |
| dc.identifier.citation | Polymers, v. 15, n. 13, 2023. | |
| dc.identifier.doi | 10.3390/polym15132952 | |
| dc.identifier.issn | 2073-4360 | |
| dc.identifier.scopus | 2-s2.0-85164733733 | |
| dc.identifier.uri | https://hdl.handle.net/11449/307336 | |
| dc.language.iso | eng | |
| dc.relation.ispartof | Polymers | |
| dc.source | Scopus | |
| dc.subject | 3D printing | |
| dc.subject | carbon nanotubes | |
| dc.subject | ceramics | |
| dc.subject | composites | |
| dc.subject | inflammatory process | |
| dc.subject | osteogenesis | |
| dc.subject | tissue engineering | |
| dc.title | Early In Vivo Osteogenic and Inflammatory Response of 3D Printed Polycaprolactone/Carbon Nanotube/Hydroxyapatite/Tricalcium Phosphate Composite Scaffolds | en |
| dc.type | Artigo | pt |
| dspace.entity.type | Publication | |
| unesp.author.orcid | 0000-0003-2832-1984[1] | |
| unesp.author.orcid | 0000-0001-5669-349X[4] | |
| unesp.author.orcid | 0000-0001-6030-1962[5] | |
| unesp.author.orcid | 0000-0002-3490-5030[6] | |
| unesp.author.orcid | 0000-0002-4418-1080[8] |

