Authors:Bernd Spangenberg and Marion Weyandt-Spangenberg
A new formula is presented for transforming fluorescence measurements in accordance with
theory. The fluorescence signals, the absorption signals, and data from a selected reference are combined in one expression. Only diode-array techniques can measure all the required data simultaneously to linearize fluorescence data correctly. To prove the new theory HPTLC quantification of the analgesic flupirtine was performed over the mass range 300 to 5000 ng per spot. The fluorescence calibration curve was linear over the whole range. The transformation of fluorescence measurements into linear mass-dependent data extends the technique of in-situ fluorescence analysis to the high concentration range. It also extends
theory from absorption to fluorescence analysis. The results presented also emphasize the importance of
theory for in-situ measurements in scattering media, especially in planar chromatography.
Authors:L. Luo, D. R. Chettle, H. Nie, F. E. McNeill, and M. Popovic
We investigated the potential application of the genetic algorithm in the analysis of X-ray fluorescence spectra from measurement
of lead in bone. Candidate solutions are first designed based on the field knowledge and the whole operation, evaluation,
selection, crossover and mutation, is then repeated until a given convergence criterion is met. An average-parameters based
genetic algorithm is suggested to improve the fitting precision and accuracy. Relative standard deviation (RSD%) of fitting
amplitude, peak position and width is 1.3-7.1, 0.009-0.14 and 1.4-3.3, separately. The genetic algorithm was shown to make
a good resolution and fitting of K lines of Pb and g elastic peaks.
Authors:M. Zamburlini, A. Pejović-Milić, and D. R. Chettle
In this study, we present a significant improvement in the minimum detection limit (MDL) for strontium measurement in bone
with X-ray fluorescence using 125I as the excitation source. The improvement was achieved thanks to a new collimator in the 90 degree geometry and a different
source positioning in the 180 degree geometry. The achieved MDL in the 90 degree geometry is 0.0426±0.0006 mg Sr/g Ca, which
is 5.5 times better than the one previously reported. In the 180 degree geometry, the new source positioning improved the
MDL from 0.118±0.004 to 0.0446±0.0009 mg Sr/g Ca.
Authors:Zorana Katanić, Lejla Atić, Dž. Ferhatović, Vera Cesar, and H. Lepeduš
Vegetative buds represent developmental stage of Norway spruce (Picea abies L. Karst.) needles where chloroplast biogenesis and photosynthetic activity begin. We used the analyses of polyphasic chlorophyll a fluorescence rise (OJIP) to compare photosystem II (PSII) functioning in vegetative buds and fully photosynthetically active mature current-year needles. Considerably decreased performance index (PIABS) in vegetative buds compared to needles pointed to their low photosynthetic efficiency. Maximum quantum yield of PSII (Fv/Fm) in buds was slightly decreased but above limited value for functionality indicating that primary photochemistry of PSII is not holdback of vegetative buds photosynthetic activity. The most significant difference observed between investigated developmental stages was accumulation of reduced primary quinine acceptor of PSII (QA−) in vegetative buds, as a result of its limited re-oxidation by passing electrons to secondary quinone acceptor, QB. We suggest that reduced electron transfer from QA− to QB could be the major limiting factor of photosynthesis in vegetative buds.
Authors:T. P. Shakhtshneider, M. A. Vasilchenko, A. A. Politov, and V. V. Boldyrev
The method of mechanical activation was used to obtain solid-state dispersions of some drugs in polyvinylpyrrolidone, polyethylene glycol and talc as carriers. Solid dispersions obtained by mechanical activation were found to have higher apparent solubilities and dissolution rates than mechanically activated drugs or their physical or eutectic mixtures with carriers used. It was shown by IR-spectroscopy and fluorescence measurements that mechanical treatment gave rise to an interaction between components which was apparently responsible for the solubilization effects observed.
Authors:Bernd Spangenberg, Klemens Lorenz, and Steffen Nasterlack
In-situ densitometry for qualitative or quantitative purposes is a key step in thin-layer chromatography. It offers a simple way of quantifying by measuring the optical density of the separated spots directly on the plate. A new TLC scanner has been developed which is able to measure TLC plates or HPTLC plates, at different wavelengths simultaneously, without destroying the plate surface. The system enables absorbance and fluorescence measurements in one run. Fluorescence measurements are possible without filters or other adjustments.The measurement of fluorescence from a TLC plate is a versatile means of making TLC analysis more sensitive. Fluorescence measurements with the new scanner are possible without filters or special lamps. Improvement of the signal-to-noise ratio is achieved by wavelength bundling. During plate scanning the scattered light and the fluorescence are both emitted from the surface of the TLC plate and this emitted light provides the desired spectral information from substances on the TLC plate. The measurement of fluorescence spectra and absorbance spectra directly from a TLC plate is based on differential measurement of light emerging from sample-free and sample-containing zones.The literature recommends dipping TLC plates in viscous liquids to enhance fluorescence. Measurement of the fluorescence and absorbance spectra of pyrene spots reveals the mechanism of enhancement of plate dipping in viscous liquids — blocked contact of the fluorescent molecules with the stationary phase or other sample molecules is responsible for the enhanced fluorescence at lower concentrations.In conclusion, dipping in TLC analysis is no miracle. It is based on similar mechanisms observable in liquids. The measured TLC spectra are also very similar to liquid spectra and this makes TLC spectroscopy an important tool in separation analysis.
Authors:N. Saleh, K. Al-Saleh, and A. Abu El-Haija
The quantitative interpretation of X-ray fluorescence /XRF/ data is often difficult because of matrix effects. The intensity of fluorescence measurement for a given element is not only dependent on the concentration of the element, but also on the mass absorption coefficients of the sample for both excitation and fluorescent radiation. In this paper, a new approach for the determination of absorption and transmission correction factors is described.
Authors:Tamás Zsom, Edina Strohmayer, Lien Phuong Le Nguyen, Géza Hitka, and Viktória Zsom-Muha
Banana is a really chilling injury sensitive product. Its sensitivity to cold temperatures generates serious practical, economical and commercial problems. Chilling injury related physiological responses of Cavendish type green banana samples stored at 2.5, 5, 10 °C and near optimal (15 °C) cold storage temperature were investigated by nondestructive optical methods (surface color and chlorophyll fluorescence measurement, DA-index® evaluation) and by the determination of the physiological reactions (respiration, ethylene production, symptom manifestation) during cold storage and the 8-day long subsequent shelf-life. The positive effects of low temperature storage were proven on mass loss, respiration and ethylene production. In case of bananas stored at 2.5–10 °C, the chilling injury related changes in chlorophyll content related DA-index®, IR-values; Fm and Fv chlorophyll fluorescence values, the L*, a*, b*, C* and hue angle color characteristics suggested clearly from day 3 the onset of chilling injury several days before the visible signs of chilling injury appeared.
A new HPTLC method has been established for separation and quantification of six given apolar, fluorescent pyrolytic heterocyclic aromatic amines (HA) of the carboline group. The mobile phase was selected by using a practical and systematic four-level optimization scheme based on the solvent classification system according to
and the PRISMA model of
et al. The amines were separated on silica gel 60 F
HPTLC plates by a multiple development with diethyl ether. Quantification by fluorescence measurement at
= 366/>400 nm was performed immediately after development. Limits of detection were in the lownanogram range. The results show that modern planar chromatography is a rapid and cost-efficient alternative method for determination of HA. The method is suitable for both screening and quantification.
Authors:E. Kowalska, J. Radomska, P. Konarski, R. Diduszko, J. Oszczudłowski, T. Opalińska, M. Więch, and Z. Duszyc
of electronic wastes (sample A – a mixture of three types of printed
circuit boards, sample B – a mixture of electronic junctions with metal
wires) were investigated using thermogravimetric analysis (TG). Thermogravimetric
and derivative thermogravimetric data (TG and DTG) give information on the
thermal stability of A and B samples and allows finding the correct conditions
for their degradation using pyrolysis in an experimental system, built on
the laboratory scale for utilization of hazardous wastes. X-ray fluorescence
measurements prove that brominated flame retardant is present in sample A,
whilst chlorinated flame retardant is a probable component of sample B. Preliminary
liquid chromatography of oil products obtained as a result of thermal waste
degradation shows that the hydrocarbons released during pyrolysis could be
used as a fuel.