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We report a novel and efficient method for the laser direct writing of two-dimensional silver structures. Multiphoton absorption of a small fraction of the output of a Ti:sapphire oscillator is sufficient to photoreduce silver nitrate in a thin film of polyvinylpyrrolidone that has been spin-coated on a substrate. The polymer can then be washed away, leaving a pattern consisting of highly interconnected silver nanoparticles. We report the characterization of the silver patterns using scanning electron and atomic force microscopies, and demonstrate the application of this technique in the creation of diffraction gratings.

Nowadays, the development of systems, devices, or methods that integrate several process steps into one multifunctional step for clinical, environmental, or industrial purposes constitutes a challenge for many ongoing research projects. Here, we present a new integrated paper based cadmium (Cd(2+)) immunosensing system in lateral flow format, which integrates the sample treatment process with the analyte detection process. The principle of Cd(2+) detection is based on competitive reaction between the cadmium-ethylenediaminetetraacetic acid-bovine serum albumin-gold nanoparticles (Cd-EDTA-BSA-AuNP) conjugate deposited on the conjugation pad strip and the Cd-EDTA complex formed in the analysis sample for the same binding sites of the 2A81G5 monoclonal antibody (mAb), specific to Cd-EDTA but not Cd(2+) free, which is immobilized onto the test line. This platform operates without any sample pretreatment step for Cd(2+) detection thanks to an extra conjugation pad that ensures Cd(2+) complexation with EDTA and interference masking through ovalbumin (OVA). The detection and quantification limits found for the device were 0.1 and 0.4 ppb, respectively, these being the lowest limits reported up to now for metal sensors based on paper. The accuracy of the device was evaluated by addition of known quantities of Cd(2+) to different drinking water samples and subsequent Cd(2+) content analysis. Sample recoveries ranged from 95 to 105% and the coefficient of variation for the intermediate precision assay was less than 10%. In addition, the results obtained here were compared with those obtained with the well-established inductively coupled plasma emission spectroscopy (ICPES) and the analysis of certificate standard samples.

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Water-soluble gold nanorods (Au NRs) have been functionalized with an N-alkylaminopyrazole ligand, 1-[2-(octylamino)ethyl]-3,5-diphenylpyrazole (PyL), that has been demonstrated able to coordinate heavy metal ions. The Nalkylaminopyrazole functionalized Au NRs have been characterized by electron microscopy and spectroscopic investigation and tested in optical detection experiments of different ions, namely, Zn 2+ , Cd 2+ , Hg 2+ , Cu 2+ , Pb 2+ , and As 3+ . In particular, the exposure of the functionalized NRs to increasing amounts of Hg 2+ ions has resulted in a gradual red-shift and broadening of the longitudinal plasmon band, up to 900 nm. Interestingly, a significantly different response has been recorded for the other tested ions. In fact, no significant shift in the longitudinal plasmon band has been observed for any of them, while a nearly linear reduction in the plasmon band intensity versus ion concentration in solution has been detected. The very high sensitivity for Hg 2+ with respect to other investigated ions, with a limit of detection of 3 ppt, demonstrates that the functionalization of Au NRs with PyL is a very effective method to be implemented in a reliable colorimetric sensing device, able to push further down the detection limit achieved by applying similar strategies to spherical Au NPs.