AVS 56th International Symposium & Exhibition | |
Biomaterial Interfaces | Thursday Sessions |
Session BI-ThP |
Session: | Biomaterial Interfaces Poster Session II (Arrays, Sensing, Micro/Nanofabrication, SPM) |
Presenter: | V. Korolkov, University of Nottingham, UK |
Authors: | V. Korolkov, University of Nottingham, UK N. Haggerty, University of Nottingham, UK M. Blunt, University of Nottingham, UK S. Allen, University of Nottingham, UK C.J. Roberts, University of Nottingham, UK S.J.B. Tendler, University of Nottingham, UK |
Correspondent: | Click to Email |
Two dimensional (2D)-controlled adsorption is a versatile tool for creating well-defined arrays of biological molecules on surfaces. Such surfaces hold potential for a wide range of future applications, including for the development of biosensors and biomolecular screening technologies. Functionalizing a surface with some periodical structure (or a network) is one promising way to spatially control the adsorption process. Hydrogen-bonded networks are reported to be well-ordered structures, presenting periodical 2D-pores suitable for the adsorption of different guest molecules, and thus may provide a reasonable template for 2D-controlled biomolecular adsorption.
Up to the present, only a few studies have focused on solution based approaches to the fabrication of H-bonded networks, and so in this study we have concentrated our efforts towards optimizing a solution based preparation procedure for perylene tetracarboxylic diimide (PTCDI)-melamine network from dimethylsulfoxide solution. Investigations of the stability of this network over different parameters, led us to a useful, reproducible technique for creation of PTCDI-melamine network over a large surface area. It was shown that temperature plays a crucial role in ordering of PTCDI and melamine molecules on the surface.
Optimal conditions for oligonucleotide adsorption into the network-pores were also determined. This work employed several complementary surface analytical techniques to image the network structure (STM, AFM) and the controlled deposition of biomolecules (AFM, XPS).