Corrosion and permanent fracture resistance of coated and conventional orthodontic wires

The corrosion processes are presumed to have negative consequences on biocompatibility, aesthetic appearance and the frictional behavior between the bracket and the guiding arch during orthodontic treatment. A group of new guiding arches are the coated orthodontic wires. The present in-vitro study investigated the corrosion behavior and permanent fracture resistance of eight coated wires of different dimensions. Five superelastic nickel titanium (NiTi) wires (Titanol® Low Force River Finish Gold and Gold 2: Forestadent Corp.; Titanol® Superelastic tooth colored: Forestadent Corp.; Bioforce Sentalloy longuard: GAC Corp.; NiTi Imagination: GAC Corp.), two -titanium-wires (TMA Low Friction longuard: Ormco Corp.; TMA Low Friction longuard Purple: Ormco Corp.) and one steel wire (Stainless Steel Imagination: GAC Corp.) were selected. For comparison reasons three uncoated arch wires (Rematitan® Lite Dimple: Dentaurum Corp.; Titanol® Low Force River Finish: Forestadent Corp.; Bioforce Sentalloy: GAC Corp.) were included in the investigation. Surface modifications were made of teflon, polyethylene and by ion implantation. The corrosion processes have been carried out by the use of a specialized electrochemical cell. In a second experimental series the wires were exposed to mechanical stresses. Finally, all wires were examined in a scanning electron microscope. The results indicated that teflon coating prevented the corrosion of the wires. As expected, the -titanium wires did not corrode either. The other wires showed rupture potentials between 187 mV and 602 mV (NHE). After mechanical stress testing the wires could be subdivided into three groups. In the first group no differences could be recognized, the second group showed changes in their crystallographic structure and in the last group the teflon coating was peeled off from the surface of the wires.     

An integrated microfabricated cell sorter

We have developed an integrated microfabricated cell sorter using multilayer soft lithography. This integrated cell sorter is incorporated with various microfluidic functionalities, including peristaltic pumps, dampers, switch valves, and input and output wells, to perform cell sorting in a coordinated and automated fashion. The active volume of an actuated valve on this integrated cell sorter can be as small as 1 pL, and the volume of optical interrogation is approximately 100 fL. Different algorithms of cell manipulation, including cell trapping, were implemented in these devices. We have also demonstrated sorting and recovery of Escherichia coli cells on the chip.     

Carbon dioxide effects on luminol and 1,10-phenanthroline chemiluminescence

Luminol and 1,10-phenanthroline are widely used chemiluminescent (CL) reagents for the analysis of a wide range of metals and inorganic and organic complexes. While the fundamental mechanism for luminol and 1,10-phenantholine chemiluminescence is understood, the analytical application of these reagents is largely empirical and often poorly described mechanistically. For example, CL signals observed from metal-luminol systems are strongly dependent on the pH of the sample, even though the final pH of the reaction mixture is controlled to a narrow range by a buffer. Other investigators report significant changes in CL signal due to freshness and the acidity of reagents. Our work shows that many of these effects are due to dissolved CO2 present or formed in the analytical system. The hypothesis that carbon dioxide plays a pivotal role in enhancing luminol CL is supported by direct manipulation of CO2(aq) concentrations by the addition of CO2(g) or carbonic anhydrase. In contrast, Cu(II) analysis using the CL reagent 1,10-phenanthroline is completely quenched in the presence of CO2(aq). A plausible mechanism for these observations involves the reaction between superoxide, produced in these analytical systems, and CO2(aq) to form the peroxycarbonate radical, *C04-. The formation of *CO4- has very important analytical implications since this species appears to enhance or quench the CL signal from luminol and 1,10-phenanthroline, respectively.     

Improved hardware and software for quick gas chromatography-olfactometry using CHARM and GC-"SNIF" analysis

A multisniffing system has been developed to allow three panelists to simultaneously participate in a GC-olfactometric analysis. This device, associated with a computerized data treatment, allows shortening CHARM and GC-"SNIF' analyses to less than 1 week and less than 1 day, respectively. The program was developed as an extension of an existing commercial chromatography data system, as usual GC processing functions are suited to the treatment of olfactograms (plots of odor response versus GC elution time). Because of the improved algorithm, the consequences of gaps in coincident responses were minimized, and the systematic use of a panel improved the repeatability of CHARM olfactograms. Comparing both methods, GC-SNIF repeatability appears to be higher than that of CHARM, as the former method uses a larger panel, but in a shorter lapse of time.     

Characterization of archaeological beeswax by electron ionization and electrospray ionization mass spectrometry

To better detect and identify beeswax in ancient organic residues from archaeological remains, we developed a new analytical methodology consisting of the analysis of (i) the trimethylsilylated organic extract by GC/MS and (ii) the crude extract by ESI-MS. Selective scanning modes, such as SIM or MRM, permit separate quantification of each chemical family (fatty acids, monoesters, monohydroxyesters, and diesters) and allow an improvement in sensitivity and selectivity, allowing the crude extract to be treated without further purification. GC/MS (SIM) was revealed to be a powerful method for the detection of components, with a detection limit down to a total lipid extract in the range of approximately 50 ng in a complex matix, such as archaeological degraded material, whereas ESI-MS/MS is instead used for the detection of nonvolatile biomarkers. Identification by GC/MS (SIM) and ESI-MS/ MS (MRM) of more than 50 biomarkers of beeswax in an Etruscan cup at the parts-per-million level provides the first evidence for the use of this material by the Etruscans as fuel or as a waterproof coating for ceramics.     

Quenched phosphorescence detection in cyclodextrin-based electrokinetic chromatography

Quenched phosphorescence detection is a sensitive detection method recently introduced in capillary zone electrophoresis. It is based on the dynamic quenching interaction of the analytes (quenchers) with a phosphorophore, 1-bromo-4-naphthalenesulfonate (BrNS), present in the separation buffer. In this study, it is shown that this detection method can also be used in cyclodextrin-based electrokinetic chromatography (CD-EKC) despite the presence in the buffer solution of cyclodextrins, which are known to reduce the luminescence quenching rate constants. Experiments indicate that BrNS mainly resides in the aqueous phase, while the analytes are distributed between both phases. In principle, the observed quenching might arise from the interaction of BrNS with uncomplexed as well as complexed analytes. However, from the dependence of the fractional quenching on the capacity factor (the normalized fractional quenching was found to be equal to the fraction of analyte in the aqueous phase), it was concluded that only aqueous-phase quenching contributes significantly to the observed quenching. Nevertheless, separation and detection can be regarded as fully compatible, because the capacity factors encountered in CD-EKC are generally low (in this study they ranged from about 0.1 to 2.5). Indeed, with nitroaromatic compounds as the target analytes, limits of detection in the 10(-8) M range were achieved.     

Vancomycin dimerization and chiral recognition studied by high-performance liquid chromatography

The retention and separation of D,L-dansylvaline enantiomers (used as test solutes) were investigated using silica gel as stationary phase and vancomycin as chiral mobile-phase additive. A retention model was developed to describe the mechanistic aspects of the interaction between solute and vancomycin in the chromatographic system. It considered the formation of vancomycin dimers both "free" in the mobile phase and adsorbed on silica. By fitting the model equation to experimental data, it appeared clearly that the approach taking into account the vancomycin dimerization described accurately the retention behavior of the compounds. The examination of the model equation parameters showed that the glycopeptide dimerization increased the enantioselectivity by a factor of approximately 3.7. This study demonstrated the preponderant role of the vancomycin dimerization on the chiral recognition process of D,L-dansylvaline. Also, an additional analysis on a vancomycin chiral stationary phase indicated that the addition of vancomycin in the mobile phase promoted a greater enantioselectivity mediated by the formation of dimers in the stationary phase.     

Optical particle sizing in backscatter

Several possibilities for the use of elastic light scattering in the backscatter range (scattering angle theta(s) > 140 deg) for determination of size, velocity, and refractive index of spherical particles are investigated. First the phase Doppler technique is considered. Numerical simulations of light scattering with the Lorenz-Mie theory are used to show that the phase Doppler technique is unsuitable for such backscatter configurations, except for special measurement conditions. The time-shift (or pulse-displacement) technique is then considered by use of the Fourier-Lorenz-Mie theory. Simulations show that up to four fractional signals can be obtained by use of the technique in backscatter, corresponding to the scattering order or modes: surface wave (long path), reflection, second-order refraction (inner path), and a mixture of second-order refraction (outer path) and surface wave (short path). Signal characteristics as a function of particle size, refractive index, and particle ellipticity are studied. Suggestions for a practical measurement instrument are put forward.