Elemental composition of hypertrophic scar and normal skin tissue using proton induced X-ray emission

Hypertrophic scars are a particular type of scar that can form after any type of dermal trauma. They are unsightly, red and elevated above normal skin level. At present no-one knows why these scars form and what form the treatment should take. Full thickness hypertrophic skin tissue as well as full thickness normal skin samples, obtained form the Restoration of Appearance and Function Trust (RAFT), Institute of Plastic Surgery, Mount Vernon Hospital, were analysed, using simultaneously both PIXE and RBS, with a 2 MeV proton beam. The epidemis was compared to the dermis on both normal and scarred tissue, and each was compared to the other, to see if there were any variations in elemental composition. In all the samples C, N and O detected by RBS and P, S, Cl, K, Ca, Fe detected by PIXE were found, In the majority of samples Zn and Cd were found, and in a few samples Sn was determined. Significant differences in concentrations, for the elements P, S, K and Cd, between the epidermis and dermis in both hypertrophic scarred and normal skin tissue were found. A difference was also detected between elemental concentrations in normal and scarred skin for the elements Ca, P, S, Fe and Cd.     

New method of anatomic localization of scintigram of various organs by simultaneous combination of emission scanning and transmission scanning]

When the photoscintillo-roentgenography is used for relating the scintigram of internal organs to the anatomic structures, this method is found to have some defects--the difference of magnification between the emission scan and the roentgenogram, the inaccuracy due to the geometric distortion of the X-ray image, the impossibility of the simultaneous photographing of the scan and the X-rays, etc. Then, to diminish the influence of these defects we improved on the photographic recording system of a dual-heal scanner, and made use of the transmission scanning method. That is, we combined the recording parts, Ch1 and Ch2, into one system, using Ch1 for the light source of transmission scan and Ch2 for that of emission scan. In this way, we managed to make the two incident rays from those light sources converge into a focus upon a film. Thus we could perform a simultaneous emission-transmission scanning, by moving, at the same time in the same direction, the scanning detector over the patient and the small radioactive source (241Am) under him. This method can be applied to any radioactive nuclide to be used in transmission scanning and emission scanning. As the result of applying this method clinically in our department, the method has proved to be very useful for anatomic localization.     

Chemical speciation of chlorine in atmospheric aerosol samples by high-resolution proton induced X-ray emission spectroscopy

Chlorine is a main elemental component of atmospheric particulate matter (APM). The knowledge of the chemical form of chlorine is of primary importance for source apportionment and for estimation of health effects of APM. In this work the applicability of high-resolution wavelength dispersive proton induced X-ray emission (PIXE) spectroscopy for chemical speciation of chlorine in fine fraction atmospheric aerosols is studied. A Johansson-type crystal spectrometer with energy resolution below the natural linewidth of Cl K lines was used to record the high-resolution Kα and Kβ proton induced spectra of several reference Cl compounds and two atmospheric aerosol samples, which were collected for conventional PIXE analysis. The Kα spectra which refers to the oxidation state, showed very minor differences due to the high electronegativity of Cl. However, the Kβ spectra exhibited pronounced chemical effects which were significant enough to perform chemical speciation. The major chlorine component in two fine fraction aerosol samples collected during a 2010 winter campaign in Budapest was clearly identified as NaCl by comparing the high-resolution Cl Kβ spectra from the aerosol samples with the corresponding reference spectra. This work demonstrates the feasibility of high-resolution PIXE method for chemical speciation of Cl in aerosols.     

Thallium-201 radioactive implant induced X-ray emission scanning of stable iodine distribution in thyroid--phantom experiment

A new method has been developed for imaging the thyroid gland by the use of 201Tl radioactive implant induced X-ray emission (RIXE). The thyroid phantom was made from two cylindrical tubes embedded in plastic neck phantom. Each tube consisted of stable iodine and 201Tl radioactive source in 10 ml water solution. Some photopeaks in the energy range from 20 to 200 ke V were scanned along a horizontal axis by the collimated Ge detector with high energy resolution. The distribution on the horizontal axis was obtained for the generated I K alpha-ray and some primary 201Tl radiations. The 201Tl RIXE scanning can provide information about the distribution of iodine with 201Tl as well as 201Tl distribution in the thyroid gland. The effectiveness of the 201Tl RIXE technique as a thyroid scanning method is discussed.     

Application of proton induced X-ray emission to the qualitative and quantitative analysis of iodine in biological samples

Particle-induced X-ray emission (PIXE) was applied to evaluate the loss of volatile elements such as iodine in biological samples. The analytical quality of the method is comparable or better than spectrophotometry, which is currently believed to be the most reliable for iodine determination. The temperature dependence of volatility loss of trace iodine was characteristic, and the feature was divided into three temperature regions. The first one, ranging from room temperature to 200 °C, showed only a slight loss below 20% on drying; the second stage, between 200 °C and 350 °C, where carbonizing processes became prominent, showed a remarkable loss up to 50%; the last one, beyond 350 °C, was accompanied by a considerable loss of iodine (more than 80%) with ashing. Even in the analysis using low temperature ashing with oxygen plasma, the loss of iodine observed was considerable (nearly 80%). The significance of these findings by PIXE in trace analysis is noted to improve analytical quality of volatile elements, such as iodine in biological, medical and also environmental fields.     

Experimental investigation of beam heating in a soft X-ray scanning transmission X-ray microscope

A variable temperature sample holder with an operational range of 15 to 200 °C and an accuracy of ±1 °C has been fabricated for scanning transmission X-ray microscopes (STXM). Here we describe the device, and use it to image the polycrystalline morphology of solid stearic acid and palmitic acid at temperatures near their respective melting points as a means of checking for possible sample heating caused by the focused X-ray beam. The melting points observed in STXM were identical to those observed by conventional methods within measurement uncertainty, even under the most extreme, high dose rate imaging conditions investigated. The beam-induced temperature rise in the sample is inferred to be below 1 °C for dose rates of up to 2.7 GGy/s.     

Assessment of atmospheric deposition of metals in Ha Noi using the moss bio-monitoring technique and proton induced X-ray emission

Journal of Radioanalytical and Nuclear Chemistry - The concentration of 22 metal elements including Mg, Al, Si, P, S, Cl, K, Ca, Ti, Cr, Mn, Fe, Ni, Cu, Zn, As, Br, Rb, Sr, Zr, Ba and Pb in Barbula...     

The determination of the elemental composition of glasses for forensic application using a combination of proton induced X-ray emission and inelastic proton scattering

Proton induced X-ray emission (PIXE) is used in an attempt to identify glass samples with the aid to determine, trace element concentrations. The elements Na and A1 are simultaneously determined using the (p, p' γ) nuclear reaction. The preparation of very thin and homogeneous glass targets is discussed and a procedure is described to obtain an accurate equipment calinration, checked afterwards with NBS bovine liver. Results are given for 11 different glass samples.     

Determination of the elemental homogeneity of selected biological organs by 2MeV proton induced X-ray emission analysis

The use of finite size sub-samples to derive elemental concentrations which are representative of a tissue or organ as a whole are subject to errors arising from the heterogeneous nature of biological specimens. Proton induced X-ray emission (PIXE) analysis is employed to identify element variances in porcine liver, kidney and heart and sampling factors, which are the minimum mass of sample required to reduce concentration variability to a given level, are calculated. This analysis highlights the inhomogeneous nature of biological specimens and the need for clearly defined sampling protocols.     

The capabilities of proton induced X-ray fluorescence in analytical chemistry

The possibility to use proton induced X-ray fluorescence in trace analysis is investigated. Sensitivities and detection limits for elements from Z=24 are determined. The influence of a NaCl matrix on these parameters is measured and some possibilities are given to use the technique in analytical practice.     

Photon and proton induced X-ray cross sections for some elements

The cross sections for the production of K and L shell x-rays in some elements by monoenergetic photons have been measured and the experimental values were compared with the theoretical values. Also, the K shell x-ray production cross sections have been measured for thin targets of some elements by protons over the energy range 1.5–3.0 MeV. The ionisation cross sections were calculated and compared with Johansson's empirical formula.     

Transmission mode ion/ion proton transfer reactions in a linear ion trap

A new method is described for effecting ion/ion proton transfer reactions that involves storage of analyte ions while oppositely charged ions are transmitted through the stored ion population. In this approach, the products are captured and stored in the linear ion trap for subsequent mass analysis. Charge reduction of multiply charged protein ions is used as an example to illustrate the analytical usefulness of this method. In another variation of the transmission mode ion/ion reaction approach, two charge inversion experiments, implemented by passing analyte ions through a population of multiply charged reagent ions in a LIT, are also demonstrated. A pulsed dual ion source approach coupled with a hybrid triple quadrupole/linear ion trap instrument was used to demonstrate these two methods. The results for ion/ion reactions implemented using these so-called "transmission mode" experiments were comparable to those acquired using the more conventional mutual storage mode, both in terms of efficiency and information content of the spectra. An advantage of transmission mode experiments compared with mutual storage mode experiments is that they do not require any specialized measures to be taken to enable the simultaneous storage of oppositely charged ions.     

A study on proton induced X-ray analysis and its application to environmental samples

Proton induced X-ray analysis has been studied by the 5 MV Van de Graaff of Tohoku University emphasizing on backing materials and angular dependence of background. The method has further been applied to analyses of some environmental samples. From experimental results, it was found that 4 μm Mylar foil among Formvar, Mylar and carbon gives sufficiently low background spectrum, high sensitivity and good mechanical strength. The detection limit is much improved at the backward direction with respect to the incident beam comparing with that at 90° which has usually been adopted. The analytical results on soil and aerosol samples were compared with those by the Atomic Absorption Spectrophotometrical method (AAS). Vanadium can easily be analysed by this method, but not by the AAS method. Milk and human milk were also analysed.     

Determination of elemental and ionic compositions for diesel exhaust particles by particle induced X-ray emission and ion chromatography analysis.

The purpose of this study is to clarify the chemical characterization of PM2.5 and PM10 in diesel exhaust particles (DEP). Sampling of PM2.5 and PM10 in DEP was carried out in November 1999 using an automobile exhaust testing system at the National Traffic Safety and Environment Laboratory, with a diesel truck (engine type: direct injection, displacement: 7,961 cc, carrying weight: 2,020 kg, equivalent inertia weight: 5,600 kg) placed on a chassis dynamometer. Sampling conditions included idling, constant speed of 40 km/h, M-15 test pattern and 60%-revolution/40%-load of maximum power. Samples were collected on a polycarbonate membrane filter (Nuclepore, pore size: 0.8 microm) using a MiniVol Portable Air Sampler (Airmetrics Co., Inc.). The concentrations of several elemental and ionic species in the PM2.5 and PM10 samples were determined by particle induced X-ray emission (PIXE) and ion chromatography analysis. PIXE analysis of the PM2.5 and PM10 samples revealed 15 elements, of which Na, Mg, Si, S, Cl, Ca, Fe and Zn were found to be the major components. Ionic species were Cl-, NO2-, NO3-, SO4(2-), Na+, NH4+, K+ and Ca2+. Concentrations of elements and ionic species under the sampling condition of 60%-revolution/40%-load were highest in comparison with those of the other sampling conditions. The elemental and ionic species data were compared for PM2.5 and PM10; PM2.5 concentrations were 70% or more of PM10 concentrations for the majority of elements, and concentrations of ionic species in PM2.5 and PM10 were almost identical.     

Charged nanoparticle dynamics in water induced by scanning transmission electron microscopy

Using scanning transmission electron microscopy we image ~4 nm platinum nanoparticles deposited on an insulating membrane, where the membrane is one of two electron-transparent windows separating an aqueous environment from the microscope's high vacuum. Upon receiving a relatively moderate dose of ~10(4) e/nm(2), initially immobile nanoparticles begin to move along trajectories that are directed radially outward from the center of the field of view. With larger dose rates the particle motion becomes increasingly dramatic. These observations demonstrate that, even under mild imaging conditions, the in situ electron microscopy of aqueous environments can produce electrophoretic charging effects that dominate the dynamics of nanoparticles under observation.     

Fluorine in fifteen GSJ geochemical reference samples as determined by proton induced gamma ray emission spectrometry /PIGE/

Fifteen geochemical reference samples /GRS/ issued from the Geological Survey of Japan have been analyzed by an automated proton induced -ray emission /PIGE/ method for fluorine. Results of determinations are reported. Values are given for many GRS that have not previously been analyzed for fluorine.     

Determination of fluorine concentrations in soil samples using proton induced gamma-ray emission

A non-destructive, in situ current normalized particle induced gamma-ray emission methodology has been standardized for quantification of fluorine (F) in soil samples from Punjab state, India. The samples were irradiated using 4 MeV proton beam from the Folded Tandem Ion Accelerator at BARC, Mumbai. The gamma rays of energies 197 and 478 keV arising from ¹⁹F(p, p′γ)¹⁹F and ⁷Li(p, p′γ)⁷Li nuclear reactions were measured using high resolution gamma-ray spectrometry. The concentration of fluorine in soil samples was found to vary between 414 and 5,746 mg kg^?1.