Surface modified materials for active capture of enzymes

Journal article

When materials contact biological fluids including blood, protein adsorption occurs rapidly and the proteins present at the interface can subsequently influence the biological response, potentially causing undesired reactions and the failure of medical devices. This thesis explores the impact of surface properties on protein attachment to materials, providing crucial insights into material functionality and the response in biological conditions. To address the lack of control of proteins at interfaces, several surface modification strategies were developed including topographical, chemical and biological methods. These approaches aim to enhance the immobilization of specific proteins on polymer surfaces and obtain an improved understanding of the interactions. Bovine serum albumin (BSA), fibrinogen (Fg), fetuin-A (Fet-A) and immunoglobulin G (IgG) served as models to investigate the protein adsorption, competitive surface affinity and immobilization efficiency on modified surfaces. These desired biomolecules were immobilized on polymers using polydopamine (PDA) and newly synthesized diazirine molecules as linkers for surface conjugation with detailed characterization performed. The results indicated that micropatterned surfaces increased protein immobilization on polydimethylsiloxane (PDMS) by providing greater surface area. PDA-modified PDMS exhibited enhanced protein capacity along with good stability and combining micropatterns with PDA improved levels further. Multiple proteins were immobilized and the amounts could be controlled through either simultaneous or sequential methods. The strength of attachment of the proteins was influenced by the surrounding biological environment based on the concentrations of proteins. For diazirine-modified surfaces, activation through thermal and ultraviolet (UV) methods significantly improved both the quantity and stability of proteins immobilized on PDMS and polyurethane (PU). The diazirine conjugation approach is applicable to other substrates and can provide benefits for intricate devices and implants. Overall, this thesis contributes new knowledge to understanding protein-material interactions and provides novel and promising strategies for modifying polymer surfaces to achieve functionalized biomaterials for various medical applications.ThesisDoctor of Philosophy (PhD

Authors: Wang, D; Hartz, WF; Moloney, MG

• Publication status: Published
• Peer review status: Peer reviewed
• Publisher: Royal Society of Chemistry
• Journal: Journal of Materials Chemistry B: Materials for biology and medicine
• Volume: 11
• Issue: 11
• Pages: 2377-2388
• Publication date: 2023-03-15
• DOI: 10.1039/d2tb02550g
• EISSN: 2050-7518
• ISSN: 2050-750X
• Language: English
• Keywords: Chemistry; Immobilized enzyme; Organic chemistry; Composite material; Membrane; Surface modification; Covalent bond; Polymer chemistry; Materials science; Biochemistry; Cellulase; Polymer; Chemical engineering; Polystyrene; Enzyme