A novel nanoporous gold modified electrode for the selective determination of dopamine in the presence of ascorbic acid.

The electrochemical detection of dopamine (DA) at conventional solid electrodes was interfered by the coexisted ascorbic acid (AA). To circumvent this problem, many modified electrodes were tried. In this paper, an attempt was made to use nanoporous gold (NPG) as modifying materials. The NPGs with different pore sizes were prepared simply by dealloying Ag from Au/Ag alloy with concentrated nitric acid. The glassy carbon electrode (GCE) based modified electrode was fabricated by simply affixing the NPG film on the surface of a GCE. The electrochemical behaviors of AA and DA at the modified electrode were studied. The results indicated that the NPG/GCE exhibited substantial enhancement in electrochemical sensitivity for DA and AA due to its large surface area. Results also showed that the oxidation of AA at the electrode was a diffusion-controlled process, but for DA it was an adsorption-controlled process. This result, together with the different anodic peak potentials of the two species, made it possible the selective determination of DA in the presence of AA. Due to the interaction of the amino group of DA with the surface of nanoscale gold, DA could be accumulated on the NPG/GCE, while AA could not. This permitted the coexistence of large amount of AA. When differential pulse voltammetry (DPV) was used, a submicrolevel of DA could be detected in the millimolar level of AA with a detection limit of 17nM at a signal-to-noise ratio of 3. In a word, the modified electrode showed good sensitivity, selectivity and reproducibility.

Catalytic activities of fungal oxidases in hydrophobic ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate-based microemulsion.

For hydrophobic ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate ([BMIM][PF(6)]), an H(2)O-in-[BMIM][PF(6)] microemulsion could be formed in the presence of nonionic surfactant Triton X-100 (TX-100). In such a medium, both lignin peroxidase (LiP) and laccase could express their catalytic activity with the optimum molar ratio of H(2)O to TX-100 at 8.0 for LiP and >20 for laccase, and the optimum pH values at 3.2 for LiP and 4.2 for laccase, respectively. As compared with pure or water saturated [BMIM][PF(6)], in which the two oxidases had negligible catalytic activity due to the strong inactivating effect of [BMIM][PF(6)] on both enzymes, the use of the [BMIM][PF(6)]-based microemulsion had some advantages. Not only the catalytic activities of both fungal oxidases greatly enhanced, but also the apparent viscosity of the medium decreased.

Catalytic performance of lignin peroxidase in a novel reverse micelle.

To enhance the catalytic activity of lignin peroxidase (LiP) in a reverse micelle, a synthesized two-tail nonionic surfactant N-gluconyl glutamic acid didecyl ester (GGDE) was used to formulate a novel reverse micelle. Based on the LiP catalyzed oxidation of veratryl alcohol (VA) in this novel GGDE/TritonX-100-cyclohexane-H(2)O reverse micelle, the effects of the size of the reverse micelle, the buffer pH, and the concentration of H(2)O(2) on the catalytic activity of LiP were investigated. Under the optimized conditions, the catalytic efficiency of LiP in the GGDE/TritonX-100 reverse micelle was 40 times higher than that in the AOT reverse micelle. The full expression of catalytic activity of LiP in this medium was mainly due to the lack of electrostatic interaction between LiP and the head group of GGDE and TritonX-100 and to the size fit between LiP and the inner water cavity of the reverse micelle.

[Studies on the catalytic performance of lignin peroxidase in nonionic reversed micelles].

Lignin peroxidase (LiP) hosted in Brij 30/cyclohexane/water nonionic reversed micelle could express its catalytic activity, but in Triton X-100/n-pentanol/cyclohexane/water nonionic reversed micelle LiP didn't show any catalytic activity. Some key factors that affected the catalytic activity of LiP in Brij 30 reversed micelle were studied at 20 degrees C. The optimum conditions were:omega0 = 8.5, pH = 2.2, [Brij30] = 600 mmol/L; under these conditions the half time of LiP was ca. 50 hours. As compared with the properties of LiP in aqueous solution, the activity of LiP hosted in Brij 30 reversed micelle dropped, but its stability improved greatly. To reveal the role of normal alcohol, which was a necessary component for forming Triton X-100 reversed micelles, the effect of n-pentanol on the catalytic activity of LiP in Brij 30 reversed micelle was investigated. Results indicated that high concentration of the alcohol deactivated LiP. So it was deduced that the phenomenon that LiP hosted in the Triton X-100 reversed micelles could not express its activity was mainly due to the alcohol co-surfactant.