An electrochemical investigation of glucose oxidase at a CdS nanoparticles modified electrode.

The direct electrochemistry of glucose oxidase (GOD) adsorbed on a CdS nanoparticles modified pyrolytic graphite electrode was investigated, where the enzyme demonstrated significantly enhanced electron-transfer reactivity. GOD adsorbed on CdS nanoparticles maintained its bioactivity and structure, and could electro-catalyze the reduction of dissolved oxygen, which resulted in a great increase of the reduction peak current. Upon the addition of glucose, the reduction peak current decreased, which could be used for glucose detection. Performance and characteristics of the fabricated glucose biosensor were assessed with respect to detection limit, sensitivity, storage stability and interference exclusion. The results showed that the fabricated biosensor was sensitive and stable in detecting glucose, indicating that CdS nanoparticle was a good candidate material for the immobilization of enzyme in glucose biosensor construction.

A novel single-layered MoS2 nanosheet based microfluidic biosensor for ultrasensitive detection of DNA.

Recently, MoS2 nanosheets were demonstrated to be able to spontaneously adsorb single-stranded DNA, acting as efficient dye quenchers. We herein report a novel microfluidic biosensor for fluorescent DNA detection based on single-layered MoS2 nanosheets. The proposed platform is simple, rapid and visible with high sensitivity and selectivity.

Enhanced electron-transfer reactivity of horseradish peroxidase in phosphatidylcholine films and its catalysis to nitric oxide.

Direct electrochemistry of horseradish peroxidase (HRP) embedded in film of phosphatidylcholine (PC) is investigated at a pyrolytic graphite electrode by voltammetric methods. The electron-transfer reactivity between incorporated HRP and the electrode is found to be greatly enhanced by phosphatidylcholine film. Cyclic voltammetry (CV) of this incorporated peroxidase shows a pair of well-defined and nearly reversible peaks, and the cathodic and anodic peak potentials are located at about -0.261 and -0.180 V, respectively versus saturated calomel electrode at pH 5.5. Ultraviolet-visible absorption spectra indicate that the heme microenvironment of HRP in phosphatidylcholine film is similar to that of its native status. It is also observed that HRP modified electrode is able to catalyze the electrochemical reduction of nitric oxide. Experimental results reveal that the peak current related to nitric oxide reduction is linearly proportional to its concentration in the ranges of 2.0 x 10(-7) -5.0 x 10(-6) mol (-1) and 2.0 x 10(-5) -1.0 x 10(-4) mol(-1), based on which an unmediated biosensor for nitric oxide is developed.

A graphene nanoribbon network and its biosensing application.

Graphene oxide nanoribbons (GONRs) have been prepared by chemically unzipping multiwalled carbon nanotubes (MWCNTs). Thin-film networks of GONRs were fabricated by spray-coating, followed by a chemical or thermal reduction to form reduced graphene oxide nanoribbons (rGONRs). Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) characterizations indicate that the thermal reduction in the presence of ethanol vapor effectively restores the graphitic structure of the GONR as compared to chemical reduction with hydrazine vapor. Electrical measurements under a liquid-gate configuration demonstrates that rGONR network field-effect transistors exhibit much higher on/off ratios than a network of microsized reduced graphene oxides (rGOs) or a continuous film of single-layered pristine or chemical vapor deposited (CVD) graphene. Furthermore, we demonstrated the potential applications of rGONR networks for biosensing, specifically, the real-time and sensitive detection of adenosine triphosphate (ATP) molecules.