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

Author:

Nalesso Paulo Roberto Lopes1ORCID,Vedovatto Matheus1,Gregório Julia Eduarda Schneider1,Huang Boyang2ORCID,Vyas Cian23ORCID,Santamaria-Jr Milton45ORCID,Bártolo Paulo23,Caetano Guilherme Ferreira146ORCID

Affiliation:

1. Graduate Program in Biomedical Sciences, University Centre of Hermínio Ometto Foundation, Araras 13607-339, SP, Brazil

2. Singapore Centre for 3D Printing, School of Mechanical and Aerospace Engineering, Nanyang Technological University, Jurong West, Singapore 639798, Singapore

3. School of Mechanical, Aerospace and Civil Engineering, The University of Manchester, Manchester M13 9PL, UK

4. Graduate Program of Orthodontics, University Centre of Hermínio Ometto Foundation, Araras 13607-339, SP, Brazil

5. Department of Social and Pediatric Dentistry, UNESP - São Paulo State University, Institute of Science and Technology - College of Dentistry, São José dos Campos 12245-000, SP, Brazil

6. Division of Dermatology, Department of Internal Medicine, Ribeirão Preto Medical School, São Paulo University (USP), Ribeirão Preto 14049-900, SP, Brazil

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.

Funder

São Paulo Research Foundation

CNPq

Engineering and Physical Sciences Research Council (UK) Doctor Prize Fellowship

Publisher

MDPI AG

Subject

Polymers and Plastics,General Chemistry

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