Integrated sensing and biosensing
microfluidic systems often require
sealing between polysiloxane, glass, and gold interfaces, while maintaining
functional support on the gold surface within the cell chamber (e.g.,
biomolecular interaction analysis). A carboxylated trimethoxysilane
(TMS-EDTA) coating has been shown to facilitate the bonding of polydimethylsiloxane
(PDMS) to gold and glass slides. In this work, the adsorption of TMS-EDTA
onto Au is characterized in order to enable its rational use in hybrid
glass/gold substrates. Surface plasmon resonance results suggest that
carboxylates are available for streptavidin immobilization. Atomic
force microscopy studies indicate that a uniform surface coverage
with monolayer thickness is formed. Infrared spectroscopy studies
confirm that the carboxyl groups are present. Moreover, there is little
evidence of siloxane cross-linking. Electrochemical differential capacitance
measurements reveal that the potential-dependent free energies of
adsorption are ∼−20 to–30 kJ/mol (for potentials
between −0.5 and 0.2 V) in the complex electrolyte solution
used. Furthermore, at highly negative potentials (∼−1.1
V), TMS-EDTA desorbs from the Au surface. The fundamental knowledge
obtained about TMS-EDTA adsorption on Au can be applied to construct
robust PDMS-based systems with hybrid glass/gold substrates.