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Early In Vivo Osteogenic and Inflammatory Response of 3D Printed Polycaprolactone/Carbon Nanotube/Hydroxyapatite/Tricalcium Phosphate Composite Scaffolds

dc.contributor.authorNalesso, Paulo Roberto Lopes
dc.contributor.authorVedovatto, Matheus
dc.contributor.authorGregório, Julia Eduarda Schneider
dc.contributor.authorHuang, Boyang
dc.contributor.authorVyas, Cian
dc.contributor.authorSantamaria-Jr, Milton [UNESP]
dc.contributor.authorBártolo, Paulo
dc.contributor.authorCaetano, Guilherme Ferreira
dc.contributor.institutionUniversity Centre of Hermínio Ometto Foundation
dc.contributor.institutionNanyang Technological University
dc.contributor.institutionThe University of Manchester
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2025-04-29T20:09:04Z
dc.date.issued2023-07-01
dc.description.abstractThe 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.affiliationGraduate Program in Biomedical Sciences University Centre of Hermínio Ometto Foundation, SP
dc.description.affiliationSingapore Centre for 3D Printing School of Mechanical and Aerospace Engineering Nanyang Technological University, Jurong West
dc.description.affiliationSchool of Mechanical Aerospace and Civil Engineering The University of Manchester
dc.description.affiliationGraduate Program of Orthodontics University Centre of Hermínio Ometto Foundation, SP
dc.description.affiliationDepartment of Social and Pediatric Dentistry UNESP - São Paulo State University Institute of Science and Technology - College of Dentistry, SP
dc.description.affiliationDivision of Dermatology Department of Internal Medicine Ribeirão Preto Medical School São Paulo University (USP), SP
dc.description.affiliationUnespDepartment of Social and Pediatric Dentistry UNESP - São Paulo State University Institute of Science and Technology - College of Dentistry, SP
dc.description.sponsorshipEngineering and Physical Sciences Research Council
dc.identifierhttp://dx.doi.org/10.3390/polym15132952
dc.identifier.citationPolymers, v. 15, n. 13, 2023.
dc.identifier.doi10.3390/polym15132952
dc.identifier.issn2073-4360
dc.identifier.scopus2-s2.0-85164733733
dc.identifier.urihttps://hdl.handle.net/11449/307336
dc.language.isoeng
dc.relation.ispartofPolymers
dc.sourceScopus
dc.subject3D printing
dc.subjectcarbon nanotubes
dc.subjectceramics
dc.subjectcomposites
dc.subjectinflammatory process
dc.subjectosteogenesis
dc.subjecttissue engineering
dc.titleEarly In Vivo Osteogenic and Inflammatory Response of 3D Printed Polycaprolactone/Carbon Nanotube/Hydroxyapatite/Tricalcium Phosphate Composite Scaffoldsen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0003-2832-1984[1]
unesp.author.orcid0000-0001-5669-349X[4]
unesp.author.orcid0000-0001-6030-1962[5]
unesp.author.orcid0000-0002-3490-5030[6]
unesp.author.orcid0000-0002-4418-1080[8]

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