Research Library

Premium Three‐dimensional printed PCL ‐hydroxyapatite scaffolds filled with CNT s for bone cell growth stimulation
Author(s)
Gonçalves Elsa M.,
Oliveira Filipe J.,
Silva Rui F.,
Neto Miguel A.,
Fernandes M. Helena,
Amaral Margarida,
ValletRegí María,
Vila Mercedes
Publication year2016
Publication title
journal of biomedical materials research part b: applied biomaterials
Resource typeJournals
PublisherWiley
Abstract A three‐phase [nanocrystalline hydroxyapatite (HA), carbon nanotubes (CNT), mixed in a polymeric matrix of polycaprolactone (PCL)] composite scaffold produced by 3D printing is presented. The CNT content varied between 0 and 10 wt % in a 50 wt % PCL matrix, with HA being the balance. With the combination of three well‐known materials, these scaffolds aimed at bringing together the properties of all into a unique material to be used in tissue engineering as support for cell growth. The 3D printing technique allows producing composite scaffolds having an interconnected network of square pores in the range of 450–700 μm. The 2 wt % CNT scaffold offers the best combination of mechanical behaviour and electrical conductivity. Its compressive strength of ∼4 MPa is compatible with the trabecular bone. The composites show typical hydroxyapatite bioactivity, good cell adhesion and spreading at the scaffolds surface, this combination of properties indicating that the produced 3D, three‐phase, scaffolds are promising materials in the field of bone regenerative medicine. © 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 104B: 1210–1219, 2016.
Subject(s)adhesion , biomedical engineering , composite material , composite number , materials science , matrix (chemical analysis) , medicine , polycaprolactone , polymer , scaffold , tissue engineering
Language(s)English
SCImago Journal Rank0.665
H-Index108
eISSN1552-4981
pISSN1552-4973
DOI10.1002/jbm.b.33432

Seeing content that should not be on Zendy? Contact us.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here