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Title: Developing protein-based bio-inks for FDM 3D printed microfluidic and millifluidic biosensor applications
Author: Sirjani, Elaheh
ISNI:       0000 0004 7968 1485
Awarding Body: University of Brighton
Current Institution: University of Brighton
Date of Award: 2019
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Protein-based bio-inks for fused deposition modelling (FDM) 3D printers were developed along with protocols for printing these bio-inks on the surface of the 3D-prints in such a way that they retain their biological activity. Firstly, physical characterisation of a range of novel FDM filaments was performed in the printed state, to provide a set of criteria to determine an optimum filament for the fabrication of a microfluidic or millifluidic (biosensor) device containing the developed bio-inks. Secondly, a custom-built syringe extruder for the MakerBot Replicator 2X experimental 3D printer was constructed and characterised. The syringe extruder was prepared to establish methodological approaches so that bio-inks could be decanted directly onto 3D prints during production. Thirdly a series of approaches were trialled to develop bio-inks for FDM 3D printed microfluidic or millifluidic biosensor application. Protein-based bio-inks were made by covalently coupling glucose oxidase and horseradish peroxidase proteins to 20 nm and 50 nm AuNPs, gold-coated magnetic nanoparticles (Nitmagold50nm) and magnetic Dynabeads. Suitability of developed bio-inks for FDM 3D printing applications was evaluated by assessing immobilisation and inhibition of bio-inks enzymatic activity in 3D printed devices using an optimised protocol. A set of functional bio-inks were successfully prepared using glucose oxidase and horseradish peroxidase protein coupled to Dynabeads, decanted into 3D printed devices using the FDM 3D printer syringe extruder, to make a simple glucose detection system. Finally, using transparent filaments 3D-printed inserts for a UV/vis spectrometer were developed and loaded with bio-inks to enable a colorimetric enzymatic cascade reaction capable of quantifying lactose in solution to be carried out. The findings of this research are a step toward creating inexpensive and rapidly produced 3D printed biosensor devices for colorimetric enzymatic assays by open source methods.
Supervisor: Dymond, Marcus ; Cragg, Peter Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID:  DOI: Not available