Saima Anjum

Electrochemical cholesterol sensor based on carbon nanotube@molecularly imprinted polymer modified ceramic carbon electrode.

A monolithic molecular imprinting sensor based on ceramic carbon electrode (CCE) has been reported. The sensor can be renewed simply by smoothing. It was fabricated by thoroughly mixing multiwalled carbon nanotube@molecularly imprinted polymer (MWCNT@MIP), graphite powder, and silicon alkoxide, and then packing the resulting complex mixture of components firmly into the electrode cavity of a Teflon sleeve. The incorporated MWCNT@MIP in CCEs functioned as a recognition element for cholesterol determination. The MWCNT@MIP-CCEs were tested in the presence or absence of cholesterol by cyclic voltammetry and linear sweep voltammetry. The cholesterol sensor has excellent sensitivity with a linear range of 10-300nM and a detection limit of 1nM (S/N=3). The monolithic molecular imprinting sensor exhibits good stability, high sensitivity, and user-friendly reusability for cholesterol determination. This study shows that CCE is a promising matrix for MIP sensors.

Synthesis and electrochemical applications of nitrogen-doped carbon nanomaterials

Abstract Nitrogen doping is an effective way to tailor the properties of the shaped carbon materials, including the nanotubes, nanocups, nanofibers, as well as the nanorods, and render their potential use for various applications. The common bonding configurations obtained on the N insertion is the pyridinic N and pyrrolic N, which impart the characteristic properties to these carbon materials. This review will focus on the nitrogen-doped carbon materials, the doping effect on the electrochemistry of the doped nanomaterials, and the various synthetic methods to introduce N into the carbon network. The potential applications of the N-doped materials are also reviewed on the basis of the experimental and theoretical studies in electrochemistry.

Fluorescent silica nanoparticle-based probe for the detection of ozone via fluorescence resonance energy transfer

A fluorescence resonance energy transfer (FRET) platform for the detection of ozone was developed by combining the overlap of the fluorescence spectrum of Ru(bpy)3(2+)-doped silica nanoparticles with the absorption spectrum of indigo carmine at around 600 nm. This FRET system can be used to detect ozone simply within 10 min. Simple qualitative ozone detection methods using cotton swabs or paper were also developed.

Fabrication of biomembrane-like films on carbon electrodes using alkanethiol and diazonium salt and their application for direct electrochemistry of myoglobin

Alkanethiols generally form self-assembled monolayers on gold electrodes and the electrochemical reduction of aromatic diazonium salts is a popular method for the covalent modification of carbon. Based on the reaction of alkanethiol with aldehyde groups covalently bound on carbon surface by the electrochemical reduction of aromatic diazonium salts, a new strategy for the modification of carbon electrodes with alkanethiols has been developed. The modification of carbon surface with aldehyde groups is achieved by the electrochemical reduction of aromatic diazonium salts in situ electrogenerated from a nitro precursor, p-nitrophenylaldehyde, in the presence of nitrous acid. By this way, in situ electrogenerated p-aminophenyl aldehyde from p-nitrophenylaldehyde immediately reacts with nitrous acid, effectively minimizing the side reaction of amine groups and aldehyde groups. The as-prepared alkanethiol-modified glassy carbon electrode was further used to make biomembrane-like films by casting didodecyldimethylammonium bromide on its surface. The biomembrane-like films enable the direct electrochemistry of immobilized myoglobin for the detection of hydrogen peroxide. The response is linear over the range of 1-600μM with a detection limit of 0.3μM.