Interference Reduction in Glucose Detection by Redox Potential Tuning: New Glucose Meter Development.

A new glucose meter was developed employing a novel disposable glucose sensor strip comprising a nicotinamide adenine dinucleotide-glucose dehydrogenase (NAD-GDH) and a mixture of Fe compounds as a mediator. An iron complex, 5-(2,5-di(thiophen-2-yl)-1H-pyrrol-1-yl)-1,10-phenanthroline iron(III) chloride (Fe-PhenTPy), was synthesized as a new mediator for the NAD-GDH system. Due to the high oxidation potential of the mediator, the detection potential was tuned to be more closely fitted toward the enzyme reaction potential, less than 400 mV (vs. Ag/AgCl), by mixing with an additional iron mediator. The impedance spectrometry for the enzyme sensor containing the mixed mediators showed an enhanced charge transfer property. In addition, a new cartridge-type glucose meter was manufactured using effective aligned-electrodes, which showed an enhanced response compared with conventional electrode alignment. The proposed glucose sensor resulted in a wide dynamic range in the concentration range of 30 - 500 mg dL(-1) with a reduced interference effect and a good sensitivity of 0.57 µA mM(-1).

Electron-transfer mediator for a NAD-glucose dehydrogenase-based glucose sensor.

A new electron-transfer mediator, 5-[2,5-di (thiophen-2-yl)-1H-pyrrol-1-yl]-1,10-phenanthroline iron(III) chloride (FePhenTPy) oriented to the nicotinamide adenine dinucleotide-dependent-glucose dehydrogenase (NAD-GDH) system was synthesized through a Paal-Knorr condensation reaction. The structure of the mediator was confirmed by Fourier-transform infrared spectroscopy, proton and carbon nucler magnetic resonance spectroscopy, and mass spectroscopy, and its electron-transfer characteristic for a glucose sensor was investigated using voltammetry and impedance spectroscopy. A disposable amperometric glucose sensor with NAD-GDH was constructed with FePhenTPy as an electron-transfer mediator on a screen printed carbon electrode (SPCE) and its performance was evaluated, where the addition of reduces graphene oxide (RGO) to the mediator showed the enhanced sensor performance. The experimental parameters to affect the analytical performance and the stability of the proposed glucose sensor were optimized, and the sensor exhibited a dynamic range between 30 mg/dL and 600 mg/dL with the detection limit of 12.02 ± 0.6 mg/dL. In the real sample experiments, the interference effects by acetaminophen, ascorbic acid, dopamine, uric acid, caffeine, and other monosaccharides (fructose, lactose, mannose, and xylose) were completely avoided through coating the sensor surface with the Nafion film containing lead(IV) acetate. The reliability of proposed glucose sensor was evaluated by the determination of glucose in artificial blood and human whole blood samples.

Activation of pluripotency genes by a nanotube-mediated protein delivery system.

The overexpression of cell reprogramming factors (Oct4, Sox2, Klf4, Nanog, and c-Myc) allows differentiated cells to revertto an earlier developmental stage. Differentiated cells can also be reprogrammed by directly delivering reprogramming proteins tagged with cell-penetrating peptides, which allow the proteins to pass through the cell membrane and into the cytoplasm-although this method has been an inefficient process. Here, we describe a novel technique for delivering reprogramming proteins into cells using titanium oxide (TiO2 ) nanotubes, which show no cytotoxic effects and do not affect cell proliferation. TiO2 nanotubes successfully transferred the above-mentioned reprogramming factors into differentiated somatic cells. After 3 weeks of treatment with protein-conjugated nanotubes, the somatic cells adopted an embryonic stem cell-like morphology and expressed activated Oct4-green fluorescent protein, a pluripotency biomarker. Our results indicate that TiO2 nanotubes can be used to directly deliver reprogramming factors into somatic cells to induce pluripotency.

Association of heart rates with stress response inventory scores in different age groups.

Many studies reported heart rate changes were associated with mental stress. Recently, a Stress Response Inventory (SRI) questionnaire has been devised to score physical, mental, and emotional symptoms related to mental stress occurred during the past two weeks. However, SRI has too many items to be asked routinely in a mobile device such as a cellular phone. Furthermore, its individual scores may not contribute equally to estimating stress levels in different age groups. Therefore, we sought to identify mental stress factors in the SRI that were associated with heart rate changes in different age groups. Subjects aged from 20 to 69 (n=369) scored a simplified SRI and then heart rates were measured. Multiple linear regression analysis was performed to detect subsets of SRI items that showed significant relationships with heart rates (p-value<0.1). We expect that these age dependent models could be used in identifying the cause of heart rate changes in a mobile application.