Design of a dual-core dual-hole fiber for hydrostatic pressure sensing

We propose a novel dual-core dual-hole fiber (DCDHF) for hydrostatic pressure sensing. Two fiber cores and two air holes are employed in the cross-section of the DCDHF. The mode coupling between two fiber cores of the DCDHF is sensitive to the pressure-induced index change which ensures the detection of the pressure applied to the DCDHF. Two large air holes are employed to enhance the pressure-induced index change for the DCDHF which essentially provides a built-in transducing mechanism to enhance the sensitivity for the DCDHF-based pressure sensor. The DCDHF-based pressure sensor is simply formed by splicing a segment of DCDHF to two segments of single mode fibers and its operation principle is introduced in details. Simulations show that there is a linear relationship between the pressure untilized on the DCDHF and the wavelength shift of the output spectrum at one fiber core of the DCDHF with a fixed length when the polarized light is injected into another fiber core of the DCDHF. DCDHFs with different structure parameters for pressure sensing are also investigated.     

A simple, high-resolution method for establishing DNA binding affinity and sequence selectivity.

Full details of the development of a simple, nondestructive, and high-throughput method for establishing DNA binding affinity and sequence selectivity are described. The method is based on the loss of fluorescence derived from the displacement of ethidium bromide or thiazole orange from the DNA of interest or, in selected instances, the change in intrinsic fluorescence of a DNA binding agent itself and is applicable for assessing relative or absolute DNA binding affinities. Enlisting a library of hairpin deoxyoligonucleotides containing all five base pair (512 hairpins) or four base pair (136 hairpins) sequences displayed in a 96-well format, a compound's rank order binding to all possible sequences is generated, resulting in a high-resolution definition of its sequence selectivity using this fluorescent intercalator displacement (FID) assay. As such, the technique complements the use of footprinting or affinity cleavage for the establishment of DNA binding selectivity and provides the information at a higher resolution. The merged bar graphs generated by this rank order binding provide a qualitative way to compare, or profile, DNA binding affinity and selectivity. The 96-well format assay (512 hairpins) can be conducted at a minimal cost (presently ca. $100 for hairpin deoxyoligonucleotides/assay with ethiduim bromide or less with thiazole orange), with a rapid readout using a fluorescent plate reader (15 min), and is adaptable to automation (Tecan Genesis Workstation 100 robotic system). Its use in generating a profile of DNA binding selectivity for several agents including distamycin A, netropsin, DAPI, Hoechst 33258, and berenil is described. Techniques for establishing binding constants from quantitative titrations are compared, and recommendations are made for use of a Scatchard or curve fitting analysis of the titration binding curves as a reliable means to quantitate the binding affinity.     

A Convenient Preparation of Diaryl Ketazines

Azines have proven useful as intermediates in the synthesis of hydrocarbons, amines, hydrazines and various heterocyclic systems¹ and, more recently, have found use as ligands in transition metal compounds². While a convenient one-step synthesis from hydrazine and ketones is available in the aliphatic series, ^1,3 such is not the case with diaryl ketones⁴. Diaryl ketazines are generally prepared by a two-step reaction via the corresponding hydrazone⁵.     

Stable attachment of redox groups for modified electrodes via cyanuric chloride

Methylaminopropylviologen (MAV) was covalently attached to glassy carbon electrodes via cyuranic chloride. X-ray photoelectron spectroscopy (XPS) analysis confirmed the presence of bound MAV on the electrode surfaces. Electrochemical experiments of these electrodes indicated that the bound MAV was stable and electrochemically active for extended periods of time in aqueous media. The surface coverage of MAV was in the range, of 2.0–3.0×10^?10 mol cm^?2.     

Some structural and thermodynamic studies of clathrate hydrates

X-ray and neutron diffraction studies show argon and krypton to preferentially form clathrate hydrates of structure II, rather than structure I as previously assumed; methane and hydrogen sulphide do form structure I. Re-examination of solid-solution thermodynamic theory shows that structure II is basically the more stable; structure I is generally formed only when the guest molecule is in the size range that favours occupancy of the 14-hedral over the 12-hedral cages. For molecules too large to enter the 12-hedra the relative stability of structure II is greatest at 0°C, in agreement with the observed sequence of change of stability of cyclopropane hydrate: I to II at –16° and II to I at 1.5°. Carbon dioxide hydrate is observed to decompose on prolonged standing at 105K in accord with the low-temperature instability predicted by Miller.     

Localized oscillators and heat conduction in clathrate hydrates

The glassy behaviour of the thermal conductivities of structure I xenon and structure II hydrate at high temperature are found to be described surprisingly well by a localized oscillator model. This observation leads to the suggestion of strong coupling between the localized vibrations of the guest with the lattice acoustic phonons. This conjecture is confirmed by a phenomenological calculation using the Anderson-Fano resonant scattering model.Published as NRCC 37248.     

High-throughput approaches to the quantitative analysis of ketoconazole, a potent inhibitor of cytochrome P450 3A4, in human plasma

Ketoconazole, an imidazole-piperazine compound, is an orally active antimycotic agent. In addition, ketoconazole is a specific inhibitor of cytochrome P450 3A4. As about 60% of oxidized drugs are biotransformed by this isoform, the potential effect of a concomitant administration of ketoconazole on drug disposition may be of interest during drug development. The present paper describes three different approaches (methods A, B, and C) to attain high-throughput sample preparation and analysis in the quantification of ketoconazole in human plasma. Method A consisted of acetonitrile precipitation in a 96-well plate, transfer of the supernatant via a Tomtec Quadra 96 Model 320, and subsequent injection onto a 50 x 4.6 mm (i.d.) Develosil Combi-RP-5 column (packed with C30 bonded silica particles). Method B consisted of an identical sample preparation to method A with the exception that a Michrom Magic Bullet(trade mark) column, 2.0 --> 0.50 mm (i.d., tapered bore) x25 mm length, was used. Lastly, in method C, a turbulent-flow chromatography (TurboFlow LC/APCI-MS/MS) module was used for the direct analysis of ketoconazole in human plasma. A Sciex API 3000 was used in methods A and B, while a Micromass Quattro LC was employed in method C. Based on the values obtained for the calibrator (standard) and quality control samples, all three protocols yielded satisfactory accuracy, precision, and reduced manual sample preparation time.