Noninvasive subsurface analysis using multiple miniaturized Raman probes, part I: basic study of thin-layered transparent models of biomedical tissues

This study describes a basic theory for reconstructing pure Raman signals of materials composing a multilayer sample from Raman spectra obtained using two types of miniaturized Raman probes. An illustrative example is demonstrated using a multilayer system of samples composed of the transparent plastics polymethylmethacrylate (PMMA) and polyethylene (PE) as a model of thin-layered biomedical tissues. When the same region of an object is measured using Raman probes with different focal properties, the Raman spectra provide different depth profile information depending on the level of light penetration. Thus, a detailed comparison of the spectra can provide an interesting opportunity to probe the differences between the layers. A simple analytic form is presented for reconstructing the pure Raman spectra of the embedded layer. The method applies an understanding of the Raman sampling volume in layered transparent materials to the interpretation of Raman spectra experimentally measured by multiple probes. The basic theory described here is necessary for the expansion of the technique to turbid media, such as biological samples, where light-scattering effects must be considered. The potential applications of the proposed method include material and catalyst subsurface probing through different embedded materials, such as assessment of silicon wafers, effective noninvasive screening for catalyst synthesis, and biomedical tissue research.     

Crystallographic, Thermoelectric, and Mechanical Properties of Polycrystalline Ba8Al x Si46−x Clathrates

The Al content dependence of crystallographic, thermoelectric, and mechanical properties is reported for polycrystalline Ba₈Al _x Si_46?x (nominal x = 15 to 17) clathrates prepared by combining arc melting and spark plasma sintering methods. The elastic constants and the coefficient of thermal expansion (CTE), which are also important properties for designing thermoelectric devices, are presented. Powder x-ray diffraction, scanning electron microscopy, and energy-dispersive x-ray spectroscopy (EDX) indicate that the type I clathrate is the major phase of the samples but impurity phases (mainly BaAl₂Si₂, Si, and Al) are included in the samples with high Al contents. The actual Al content x determined by EDX ranges from approximately 14 to 15. The absolute value of the Seebeck coefficient increases and the electrical conductivity decreases as the Al content increases. The changes in Seebeck coefficient and electrical conductivity are explained in terms of the dependence of the carrier concentration on the Al content. The elastic constants and the CTE of the samples depend weakly on the Al content. Some of the properties are compared with reported data of single crystals of Ba₈Al₁₆Ge₃₀, Ba₈Ga₁₆Ge₃₀, Sr₈Ga₁₆Ge₃₀, silicon, and germanium as standard references. The effective mass, Hall carrier mobility, and lattice thermal conductivity, which govern the transport properties, are determined to be ~ 2.4m ₀, ~ 7 cm² V^?1 s^?1, and ~ 1.3 W m^?1 K^?1, respectively, for actual Al content x of about 14.77. The thermoelectric figure of merit ZT is estimated to be about 0.35 at 900 K for actual Al content x of about 14.77.     

Non-occupational lead and cadmium exposure of adult women in Bangkok, Thailand

This survey was conducted to examine the extent of the exposure of Bangkok citizens to lead (Pb) and cadmium (Cd), and to evaluate the role of rice as the source of these heavy metals. In practice, 52 non-smoking adult women in an institution in the vicinity of Bangkok, volunteered to offer blood, spot urine, boiled rice and 24-h total food duplicate samples. Samples were wet-ashed, and then analyzed for Pb and Cd by ICP-MS. Geometric means for the levels in blood (Pb-B and Cd-B) and urine (Pb-U and Cd-U as corrected for creatinine concentration), and also for dietary intake (Pb-F and Cd-F) were 32.3 micrograms/l for Pb-B, 0.41 microgram/l for Cd-B, 2.06 micrograms/g creatinine for Pb-U, 1.40 micrograms/g creatinine for Cd-U, 15.1 micrograms/day for Pb-F and 7.1 micrograms/day for Cd-F. Rice contributed 30% and 4% of dietary Cd and Pb burden, respectively. When compared with the counterpart values obtained in four neighboring cities in southeast Asia (i.e. Nanning, Tainan, Manila, and Kuala Lumpur), dietary Pb burden of the women in Bangkok was middle in the order among the values for the five cities. Pb level in the blood was the lowest of the levels among the five cities and Pb in urine was also among the low group. This apparent discrepancy in the order between Pb-B (i.e. the fifth) and Pb-F (the third) might be attributable to recent reduction of Pb levels in the atmosphere in Bangkok. Regarding Cd exposure, Cd levels in blood and urine as well as dietary Cd burden of Bangkok women were either the lowest or the next lowest among those in the five cities.     

Lubrication of Si3N4 and Al2O3 in water with and without addition of silane coupling agents in the range of 0.05–0.10 mol/l

To improve water lubrication of ceramics at a lower sliding velocity, the effect of the addition of silane coupling agents was investigated. Si₃N₄ and Al₂O₃ were slid against themselves in water with and without the addition of silane coupling agents in amounts ranging from 0.05 to 0.10 mol/l. Silane coupling agents containing one or more amino groups were effective in reducing the friction of Si₃N₄ and Al₂O₃ in water. Si₃N₄ also showed significant wear reduction but not Al₂O₃. However, the addition of a silane coupling agent containing an epoxy group increased both friction and wear of Si₃N₄. Improved lubricative characteristics of Si₃N₄ in water and in silane coupling agent solutions were obtained when Si₃N₄ contained smaller amounts of sintering additives. The adsorption behaviour of a silane coupling agent on ceramics was examined using both Fourier transform infrared spectroscopy and thin layer chromatography to clarify the interaction between the silane coupling agent and the ceramics. The role of polysiloxane film formation on ceramics is discussed to demonstrate the lubrication properties of ceramics.     

Hydration behavior of perfluorinated and hydrocarbon-type proton exchange membranes: Relationship between morphology and proton conduction

The relationships between morphology and proton conduction for Nafion membranes and hydrocarbon-type proton exchange membranes, namely, sulfonated poly(arylene ether ether ketone) (S-PEEK) and sulfonated poly(arylene ether sulfone) (S-PES), were investigated by small-angle X-ray scattering (SAXS) and atomic force microscopy (AFM). The direct simultaneous observation of surface morphology and active regions of proton conduction on membranes by combined high-resolution AFM phase imaging and an electrochemical technique at controlled humidity provided significant morphological information, particularly for the hydrocarbon-type membranes that exhibit few or no features on SAXS profiles. For the Nafion membranes, the active proton paths became denser and congregated with each other at over 60% RH, resulting in the formation of well-connected networks. For the hydrocarbon-type membranes, however, only the relatively small and dispersed proton paths were observed, which showed no significant change even as water content increased. We have demonstrated that the differences in microscopic morphology between the Nafion and hydrocarbon-type membranes are associated with the differences between their macroscopic proton conductivities.     

Comparison of plasma lidocaine concentrations after injection of a fixed small volume in the stellate ganglion, the lumbar epidural space, or a single intercostal nerve

Carpal tunnel syndrome may be caused by repeated or sustained elevated carpal tunnel pressure. This study examined the relationship between carpal tunnel pressure, posture, and fingertip load. In 20 healthy individuals, carpal tunnel pressure was measured with a catheter inserted into the carpal tunnel of the dominant hand and connected to a pressure transducer. With the wrist in a pressure-neutral position, the subjects pressed on a force transducer with the index finger to levels of 0, 5, 10, and 15 N. They then pinched the transducer at the same levels of force. For both fingertip-loading postures, the carpal tunnel pressure increased with increasing fingertip load. Carpal tunnel pressures were significantly greater (p < 0.015) for the pinching task (14.2, 29.9, 41.9, and 49.7 mm Hg [1.89, 3.99, 5.59, and 6.63 kPa] for 0, 5, 10, and 15 N force levels, respectively) than for simple finger pressing (7.8, 14.1, 20.0, and 33.8 mm Hg [1.04, 1.88, 2.67, and 4.51 kPa]). This study indicates that although the external load on the finger remained constant between the two tasks, the internal loading, as measured by carpal tunnel pressure, experienced a near 2-fold increase by using a pinch grip. These findings should be given consideration in designing work tasks and tools because relatively low fingertip forces, especially in a pinch grip, elevate carpal tunnel pressures to levels that, if prolonged, may lead to the development or exacerbation of carpal tunnel syndrome.     

Permeability of vitamin B-12 in chitosan membranes. Effect of crosslinking and blending with poly(vinyl alcohol) on permeability

The permeability and diffusion of vitamin B-12 in chitosan, crosslinked chitosans, and chitosan/poly(vinyl alcohol) (PVA) blends were studied using “lag time” technique. Apparently the diffusion coefficient, D, for both crosslinked and blended chitosan membranes depends solely upon the equilibrium swelling ratio, Q, of the material in water. The functional dependence of D on Q was obtained from the data. The partition coefficients calculated for vitamin B-12 in all membranes studied were nearly constant (K ≈ 0.4). The results are shown to be consistent with the “pore type” transport mechanism for vitamin B-12 in these chitosan membranes.     

Effects of sample orientation on nonpiloted ignition of thin poly(methyl methacrylate) sheets by a laser: 2. Experimental results

The effect of the sample orientation angle on frontside (irradiated surface) ignition and subsequent backside (nonirradiated surface) flame appearance over thin poly(methyl methacrylate) (PMMA) sheets having thicknesses of 0.2 and 0.5 mm has been experimentally investigated, using a CO₂ laser as an external radiant source in quiescent normal gravity. The sample orientation angle was varied from θ=−90° (ceiling configuration) to +90° (floor configuration) at intervals of 15° under three different laser powers of 16.0, 17.3, and 26.1 W. The shortest frontside ignition delay time was observed for the ceiling configuration (θ=−90°) and frontside ignition delay time significantly varied with increase in sample orientation angle at a laser power of 16.0 W. As the laser power was increased, frontside ignition was observed at all angles and its delay time became less dependent on the sample orientation angle. The appearance of a backside flame was achieved after the formation of an open hole (due to local consumption of the sample) by two different processes: the onset of laser induced ignition over the backside sample (backside ignition) and a flame traveling from the frontside through an open hole to the backside (backside flame). The former process was observed for a limited number of cases only around the vertical configurations (−30°?θ?30°). The delay time for the appearance of backside flame tended to be longer for sample surfaces facing downward (θ°<0) than for the sample surface facing upward (θ?0°) regardless of the laser power. When the duration of laser irradiation was shortened from 10 to 4 s, as soon as the laser was shut off, the flame on the frontside immediately shrank, moved close to the sample surface, and then traveled rapidly to the backside. Therefore, the delay time of backside flame appearance (about 6 s) became longer with longer duration of laser irradiation after the onset of a frontside flame. The size of the hole (about 4 mm diameter) was large enough for the flame to travel through it, even after 4 s of laser irradiation to sample. These results indicate that the size of the hole appears to be not a critical parameter for the appearance of the backside flame.     

Nanotrap and mass analysis of aromatic molecules by phenyl group-modified nanoparticle

To functionalize the surface of nanoparticles with phenyl groups for subsequent cross-linking with aromatic molecules by mutual interactions, we prepared functional nanoparticles (d = 3 nm) by silanization with phenyl-triethoxysilane. The nanoparticles had Fe(2)O(3) cores conjugated to phenyl groups; this was confirmed by Fourier transform infrared (FT-IR) spectroscopy and absorption spectrophotometry. The typical C-H and C-C peaks and the absorption at 240 nm, which corresponds to aromatic rings, were detected in the spectroscopic results for the phenyl group-modified nanoparticles. The nanoparticles could ionize aromatic (colchicine, reserpine, and bradykinin peptide) and nonaromatic (L-α-phosphatidylethanolamine,dioleoyl, and polyethylene glycol) molecules by nanoparticle-assisted laser desorption/ionization mass spectrometry. The nanoparticles worked as a selective trap and an ionization-assisting reagent in mass spectrometry for the aromatic molecular targets.