PhD (Oct'06 - Dec'09)Bioresource Processing Research Institute of Australia (BioPRIA) and Australian Pulp and Paper Institute (APPI) Department of Chemical Engineering, Clayton, Australia, VIC 3800 PhD Project: Bioactive Papers: Printing, Activity and Stability Supervisor: Prof. Gil Garnier Co-supervisor: Dr. Wei Shen Key Features:>> Non-contact Delivery of Biomolecules >> Delivery Bio Ink using Ink Jet Printing - Characterization of Rheological Properties of Bio Ink - Control Ink Delivery System - Control Colour-Management >> Investigate Liquid-Liquid and Solid-Liquid Interaction >> Develop Concentration Gradient of Growth Factor to Guide Neuron Stem Cells >> Reaction Kinetics of Bioactive Papers >> Thermal Stability of Bioactive Papers >> Kinetics of Thermal Denaturation of Bioactive Papers >> Paper Diagnostics: Blood Type Detection Device Outline: PhD ProjectThe benefits of many breakthroughs in biotechnology, medicine and environmental science have been restricted by the high cost and the limited availability of tests and materials. Most methods developed in the laboratory are difficult to scale up for mass production manufacturing. There is a need for low cost bioassays for single used application, in health and environmental diagnostics. Disposable materials for routine bioassays for the early detection of cancers and genetic conditions, glucose in blood, and for instant water analysis of heavy metals and microbial activities, are potential applications. Successful commercialization requires bioassays to be low cost, which is usually achieved through high volume manufacturing and by choosing commodity materials. Paper and printing are two technologies meeting these criteria. Paper, a non-woven made of cellulosic fibres, easy to functionalise, biodegradable, sterilise, biocompatible and cheap. Printing is a high speed technology, highly adaptive and able to deliver patterns of materials such as functional fluids with high accuracy. Ink jet, a non-contact printing, is a technique for biomolecular deposition with precise lateral resolution, reduced contamination, better throughput and low cost advantages. The above suggests that paper is the natural material of choice for the production of disposable bioassay devices. However, the biotechnology industry has limited understanding of the stability and reactivity of bioactive papers that need to be shipped and stored.
Enzymes are model biomolecules of choice for a fundamental study because of their stereo-specificity, wide range, availability and application to functional surfaces in diagnostics and industrial processes. In this study, two enzymes: Alkaline Phosphatase (ALP) and Horseradish Peroxidase (HRP) were selected as model biomolecules. The reaction kinetics, thermal stability, functionality and selectivity of enzymatic bioactive papers were investigated. The morphology of bioactive papers was analyzed using small angle scattering (SAXS) diffraction of synchrotron light. Three types of polymer: cationic, anionic and neutral, were used to improve the enzyme fixation on paper. The reactivity and thermal stability of enzymes adsorbed on paper were measured using a colorimetric technique quantifying the intensity of the enzyme-substrate product complex. The enzyme adsorbed on paper retains its functionality and selectivity. Adsorption of enzymes on paper increased the enzyme thermal stability compared to the same enzyme in solution. Complex patterns of enzymes were also printed using a thermal inkjet printer to demonstrate the concept of paper-based bioassays manufacturing. The printed enzymes remained active. Paper is shown to be an ideal material for functional bioactive surfaces.
| With my PhD Supervisor Prof. Gil Garnier
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