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Gustavo Rivas

Publications and source records attributed to Gustavo Rivas.

2 recordsLinked to original sources

Encoded beads for electrochemical identification.

Encoded redox beads, based on the encapsulation of different quantum dots (QD) within polystyrene microspheres, have been developed for electrochemical identification. Encoded redox rods, prepared by sequential plating of different metal tracers into the pores of a host membrane, have also been designed. By incorporating different predetermined levels of multiple metal markers, such redox-encoded particles lead to a large number of recognizable voltammetric signatures and, hence, offer great promise for covert tagging of commercial products. The resulting voltammetric signatures correlate well with the predetermined loading ratio, indicating a reproducible encapsulation process. As desired for effective authenticity testing, QD-based "identification layers" were reproducibly cast and removed from packages of commercial products to display their distinct voltammetric profiles. Factors affecting the preparation of such identification layers were optimized.

Journal Article↗

Dual enzyme electrochemical coding for detecting DNA hybridization.

Enzyme-based hybridization assays for the simultaneous electrochemical measurements of two DNA targets are described. Two encoding enzymes, alkaline phosphatase and beta-galactosidase, are used to differentiate the signals of two DNA targets in connection to chronopotentiometric measurements of their electroactive phenol and alpha-naphthol products. These products yield well-defined and resolved peaks at +0.31 V (alpha-naphthol) and +0.63 V (phenol) at the graphite working electrode (vs. Ag/AgCl reference). The position and size of these peaks reflect the identity and level of the corresponding target. The dual target detection capability is coupled to the amplification feature of enzyme tags (to yield fmol detection limits) and with an efficient magnetic removal of non-hybridized nucleic acids. Proper attention is given to the choice of the substrates (for attaining well resolved peaks), to the activity of the enzymes (for obtaining similar sensitivities), and to the selection of the enzymes (for minimizing cross interferences). The new bioassay is illustrated for the simultaneous detection of two DNA sequences related to the BCRA1 breast-cancer gene in a single sample in connection to magnetic beads bearing the corresponding oligonucleotide probes. Prospects for electrochemical coding of multiple DNA targets are discussed.

Alkaline Phosphatase↗