posted on 2024-11-12, 14:08authored byJeremy Nicolas Dinoro
Since the advent of Tissue Engineering (TE) in the late 1980’s, significant progress has been made within the biomedical landscape. A recently established branch within TE is biofabrication, a field that aims to automate the fabrication of biologically functional materials through the use of additive manufacturing or three-dimensional (3D) printing, among other techniques. Additive manufacturing offers fine control over part porosity, with the capacity to match the complex internal architecture of human bone. Coupled with clinical 3D scanning techniques, 3D printing has the capacity to generate implants that accurately match defected areas. However, due to the limited number of regulatory approved devices for human implantation and high cost of sophisticated powder bed fusion printers, the printing techniques are restricted. To be compatible with regulatory requirements, this work aims to utilise a widely accessible and regulatory approved device, high-density polyethylene (HDPE) to generate bone substitutes. HDPE in the form of StarPore® supplied by industry collaborator Anatomics Pty Ltd, a three-pronged star or trilobal shape, is an established material approved by both the Federal Drug Administration (FDA) in the United States of America and the Therapeutic Goods Administration (TGA) in Australia as a bone substitute for human implantation.
History
Year
2022
Thesis type
Doctoral thesis
Faculty/School
Intelligent Polymer Research Institute
Language
English
Disclaimer
Unless otherwise indicated, the views expressed in this thesis are those of the author and do not necessarily represent the views of the University of Wollongong.