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In vitro investigations on the effects of graphene and graphene oxide on polycaprolactone bone tissue engineering scaffolds

In vitro investigations on the effects of graphene and graphene oxide on polycaprolactone bone tissue engineering scaffolds
In vitro investigations on the effects of graphene and graphene oxide on polycaprolactone bone tissue engineering scaffolds
Polycaprolactone (PCL) scaffolds that are produced through additive manufacturing are one of the most researched bone tissue engineering structures in the field. Due to the intrinsic limitations of PCL, carbon nanomaterials are often investigated to reinforce the PCL scaffolds. Despite several studies that have been conducted on carbon nanomaterials, such as graphene (G) and graphene oxide (GO), certain challenges remain in terms of the precise design of the biological and nonbiological properties of the scaffolds. This paper addresses this limitation by investigating both the nonbiological (element composition, surface, degradation, and thermal and mechanical properties) and biological characteristics of carbon nanomaterial-reinforced PCL scaffolds for bone tissue engineering applications. Results showed that the incorporation of G and GO increased surface properties (reduced modulus and wettability), material crystallinity, crystallization temperature, and degradation rate. However, the variations in compressive modulus, strength, surface hardness, and cell metabolic activity strongly depended on the type of reinforcement. Finally, a series of phenomenological models were developed based on experimental results to describe the variations of scaffold’s weight, fiber diameter, porosity, and mechanical properties as functions of degradation time and carbon nanomaterial concentrations. The results presented in this paper enable the design of three-dimensional (3D) bone scaffolds with tuned properties by adjusting the type and concentration of different functional fillers.
2096-5524
651-669
Hou, Yanhao
fb285a4f-8235-429a-9095-31468811802a
Wang, Weiguang
0cc699c0-e7b3-49d0-8c84-1e9d63f747d8
Bartolo, Paulo
2c085472-871d-4ac1-8767-23e5fe9703cf
Hou, Yanhao
fb285a4f-8235-429a-9095-31468811802a
Wang, Weiguang
0cc699c0-e7b3-49d0-8c84-1e9d63f747d8
Bartolo, Paulo
2c085472-871d-4ac1-8767-23e5fe9703cf

Hou, Yanhao, Wang, Weiguang and Bartolo, Paulo (2024) In vitro investigations on the effects of graphene and graphene oxide on polycaprolactone bone tissue engineering scaffolds. Bio-Design and Manufacturing, 651-669. (doi:10.1007/s42242-024-00280-8).

Record type: Article

Abstract

Polycaprolactone (PCL) scaffolds that are produced through additive manufacturing are one of the most researched bone tissue engineering structures in the field. Due to the intrinsic limitations of PCL, carbon nanomaterials are often investigated to reinforce the PCL scaffolds. Despite several studies that have been conducted on carbon nanomaterials, such as graphene (G) and graphene oxide (GO), certain challenges remain in terms of the precise design of the biological and nonbiological properties of the scaffolds. This paper addresses this limitation by investigating both the nonbiological (element composition, surface, degradation, and thermal and mechanical properties) and biological characteristics of carbon nanomaterial-reinforced PCL scaffolds for bone tissue engineering applications. Results showed that the incorporation of G and GO increased surface properties (reduced modulus and wettability), material crystallinity, crystallization temperature, and degradation rate. However, the variations in compressive modulus, strength, surface hardness, and cell metabolic activity strongly depended on the type of reinforcement. Finally, a series of phenomenological models were developed based on experimental results to describe the variations of scaffold’s weight, fiber diameter, porosity, and mechanical properties as functions of degradation time and carbon nanomaterial concentrations. The results presented in this paper enable the design of three-dimensional (3D) bone scaffolds with tuned properties by adjusting the type and concentration of different functional fillers.

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Accepted/In Press date: 27 March 2024
e-pub ahead of print date: 2 August 2024
Published date: September 2024

Identifiers

Local EPrints ID: 503446
URI: http://eprints.soton.ac.uk/id/eprint/503446
ISSN: 2096-5524
PURE UUID: 1cdad7d3-2b9d-4493-aff0-be222967b99b
ORCID for Weiguang Wang: ORCID iD orcid.org/0000-0002-8959-329X

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Date deposited: 01 Aug 2025 16:30
Last modified: 22 Aug 2025 02:46

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Contributors

Author: Yanhao Hou
Author: Weiguang Wang ORCID iD
Author: Paulo Bartolo

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