Daniela Zane

Green synthesis of gold-chitosan nanocomposites for caffeic acid sensing.

In this work, colloidal gold nanoparticles (AuNPs) stabilized into a chitosan matrix were prepared using a green route. The synthesis was carried out by reducing Au(III) to Au(0) in an aqueous solution of chitosan and different organic acids (i.e., acetic, malonic, or oxalic acid). We have demonstrated that by varying the nature of the acid it is possible to tune the reduction rate of the gold precursor (HAuCl(4)) and to modify the morphology of the resulting metal nanoparticles. The use of chitosan, a biocompatible and biodegradable polymer with a large number of amino and hydroxyl functional groups, enables the simultaneous synthesis and surface modification of AuNPs in one pot. Because of the excellent film-forming capability of this polymer, AuNPs-chitosan solutions were used to obtain hybrid nanocomposite films that combine highly conductive AuNPs with a large number of organic functional groups. Herein, Au-chitosan nanocomposites are successfully proposed as sensitive and selective electrochemical sensors for the determination of caffeic acid, an antioxidant that has recently attracted much attention because of its benefits to human health. A linear response was obtained over a wide range of concentration from 5.00 × 10(-8) M to 2.00 × 10(-3) M, and the limit of detection (LOD) was estimated to be 2.50 × 10(-8) M. Moreover, further analyses have demonstrated that a high selectivity toward caffeic acid can be achieved without interference from catechin or ascorbic acid (flavonoid and nonphenolic antioxidants, respectively). This novel synthesis approach and the high performances of Au-chitosan hybrid materials in the determination of caffeic acid open up new routes in the design of highly efficient sensors, which are of great interest for the analysis of complex matrices such as wine, soft drinks, and fruit beverages.

Gold and TiO2 Nanostructurated Surfaces for Assembling of Electrochemical Biosensors

Devices based on nanomaterials are emerging as a powerful and general class of ultrasensitive sensors for the direct detection of biological and chemical species. In this work, we report the preparation and the full characterization of nanomaterials such as gold nanowires and TiO2 nanostructured films to be used for assembling of electrochemical biosensors. Gold nanowires were prepared by electroless deposition within the pores of polycarbonate particle track-etched membranes (PTMs). Glucose oxidase was deposited onto the nanowires using self-assembling monolayer as an anchor layer for the enzyme molecules. Finally, cyclic voltammetry was performed for different enzymes to test the applicability of gold nanowires as biosensors. Considering another interesting nanomaterial, the realization of functionalised TiO2 thin films on Si substrates for the immobilization of enzymes is reported. Glucose oxidase and horseradish peroxidase immobilized onto TiO2-based nanostructured surfaces exhibited a pair of well-defined and quasireversible voltammetric peaks. The electron exchange between the enzyme and the electrodes was greatly enhanced in the TiO2 nanostructured environment. The electrocatalytic activity of HRP and GOD embedded in TiO2 electrodes toward H2O2 and glucose, respectively, may have a potential perspective in the fabrication of third-generation biosensors based on direct electrochemistry of enzymes.

Nanoparticles and Nanocomposites in Electrochemical Sensing Area

In the last decades, gold nanoparticles (AuNPs) have received an increasing attention due to their unique physical and chemical properties, which make them of considerable interest for applications in many fields, such as biotechnology, optics, electronics and catalysis. In this paper, we present study on the design of different-AuNPs nanocomposites, with tailored morphological properties as sensing platform able to interact directly and specifically with molecules of biological interest. To prepare these materials, we have used a facile and green route which allows tuning the morphological and electrochemical properties of AuNPs, stabilized in different dispersing media