Biosensing scaffolds with hierarchical architecture for musculoskeletal repair

Lead Research Organisation: University of Nottingham
Department Name: Sch of Pharmacy

Abstract

A key criteria to the success of any biomaterials based regenerative medicine therapy is the ability of new tissue, including vasculature, to fully penetrate the biomaterial allowing integration of the growing implant within the defect site and with surrounding tissue. The main aim of this project is to produce scaffolds which transform biomaterials from passive mechanical supports to active components of regenerative medicine. To achieve this, new 3D scaffold production approaches over multiple length scales that allow hierarchical to structures to be realised within a single scaffold will be explored. We have developed 3D printing techniques allowing the printing of highly porous microparticles with defined architecture. Such technology will allow us to construct porous microparticle based scaffolds with hierarchical architecture to control tissue ingress.
The production of biomimetic scaffolds which have bio-reporting capacity to provide feedback on tissue functionality in a non-invasive manner forms the second aim of this PhD project. Polymer synthesis strategies previously demonstrated in bacterial cells will be explored for exploitation with mammalian cells. Such polymers will be embedded within the 3D printed microparticles during fabrication to provide sensor molecules suitable for in situ SORS detection.

Publications

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Studentship Projects

Project Reference Relationship Related To Start End Student Name
EP/N50970X/1 01/10/2016 30/09/2021
1966340 Studentship EP/N50970X/1 01/10/2017 30/06/2021 Jason Hutchinson
 
Description The current results of this research include the establishment and optimisation of a protocol for achieving mesenchymal stem cell culture with two-photon lithography produced structures including materials analysis and post-processing techniques for optimal cell response. Methods have been achieved to enhance two-photon fabrication time and efficiency as well as techniques to liberate bound structures for free-floating cell culture as well as ways to isolate cell growth only to structures within a static culture. Various microparticle based geometric designs have been screened and analysed for stem cell expansion and certain geometries have been identified as having enhanced stem cell expansion capabilities in comparison to smooth and flat controls. Current work analysing stem cell markers upon "hit" geometries will identify if these structures can control stem cell differentiation through mechanobiological manipulation.
Exploitation Route These outcomes of this research will hopefully add to the current body of knowledge of how stem cells differentiate in response to biophysical cues and potentially inspire a next-generation approach towards microparticle design and microcarrier technology. This research has identified too many potential lines of questioning to pursue within one PhD project and as such could lead to a variety of other projects with more specific focuses including exploration of different tissue types, cell lines, architectural designs, material chemistries, functionalisations, drug delivery and biosensor applications.
Sectors Healthcare,Manufacturing, including Industrial Biotechology,Pharmaceuticals and Medical Biotechnology