Synthesis of Iron Oxides by Co2 Laser vs. Thermally Induced Decomposition of Inorganic Salts

This paper reports on the synthesis of various iron oxides by the IR laser processing of different iron salts. X-ray diffraction techniques were used to characterize the reaction products. Some differences in terms of crystallite size and isotropy between these oxides and those obtained from the same salt by thermal means are described and explained. This revised version was published online in July 2006 with corrections to the Cover Date.     

Qualitative and quantitative determination of human biomarkers by laser photoacoustic spectroscopy methods

The hypothesis that blood, urine and other body fluids and tissues can be sampled and analyzed to produce clinical information for disease diagnosis or therapy monitoring is the basis of modern clinical diagnosis and medical practice. The analysis of breath air has major advantages because it is a non-invasive method, represents minimal risk to personnel collecting the samples and can be often sampled. Breath air samples from the human subjects were collected using aluminized bags from QuinTron and analyzed using the laser photoacoustic spectroscopy (LPAS) technique. LPAS is used to detect traces of ethylene in breath air resulting from lipid peroxidation in lung epithelium following the radiotherapy and also traces of ammonia from patients subjected to hemodialysis for treatment of renal failure. In the case of patients affected by cancer and treated by external radiotherapy, all measurements were done at 10P(14) CO₂ laser line, where the ethylene absorption coefficient has the largest value (30.4 cm⁻¹ atm⁻¹), whereas for patients affected by renal failure and treated by standard dialysis, all measurements were performed at 9R(30) CO₂ laser line, where the ammonia absorption coefficient has the maximum value of 57 cm⁻¹ atm⁻¹. The levels of ethylene and ammonia in exhaled air, from patients with cancer and renal failure, respectively, were measured and compared with breath air contents from healthy humans. Human gas biomarkers were measured at sub-ppb (parts per billion) concentration sensitivities. It has been demonstrated that LPAS technique will play an important role in the future of exhaled breath air analysis. The key attributes of this technique are sensitivity, selectivity, fast and real time response, as well as its simplicity.     

Ethylene and ammonia traces measurements from the patients’ breath with renal failure via LPAS method

The application of laser photoacoustic spectroscopy (LPAS) for fast and precise measurements of breath biomarkers has opened up new promises for monitoring and diagnostics in recent years, especially because breath test is a non-invasive method, safe, rapid and acceptable to patients. Our study involved assessment of breath ethylene and breath ammonia levels in patients with renal failure receiving haemodialysis (HD) treatment. Breath samples from healthy subjects and from patients with renal failure were collected using chemically inert aluminized bags and were subsequently analyzed using the LPAS technique. We have found out that the composition of exhaled breath in patients with renal failure contains not only ethylene, but also ammonia and gives valuable information for determining efficacy and endpoint of HD.     

Evaluation of ammonia absorption coefficients by photoacoustic spectroscopy for detection of ammonia levels in human breath

Photoacoustic spectroscopy represents a powerful technique for measuring extremely low absorptions independent of the path length and offers a degree of parameter control that cannot be attained by other methods. We report precise measurements of the ammonia absorption coefficients at the CO₂ laser wavelengths by using a photoacoustic (PA) cell in an extracavity configuration and we compare our results with other values reported in the literature. Ammonia presents a clear fingerprint spectrum and high absorption strengths in the CO₂ wavelengths region. Because more than 250 molecular gases of environmental concern for atmospheric, industrial, medical, military, and scientific spheres exhibit strong absorption bands in the region 9.2–10.8 μm, we have chosen a frequency tunable CO₂ laser. In the present work, ammonia absorption coefficients were measured at both branches of the CO₂ laser lines by using a calibrated mixture of 10 ppm NH₃ in N₂. We found the maximum absorption in the 9 μm region, at 9R(30) line of the CO₂ laser. One of the applications based on the ammonia absorption coefficients is used to measure the ammonia levels in exhaled human breath. This can be used to determine the exact time necessary at every session for an optimal degree of dialysis at patients with end-stage renal disease.     

DKDP Crystals for Electrooptic Devices

The deuterated homologue of potassium dihydrogen phosphate crystals (DKDP) was grown by a modified transport method. Experimental results concerning electrooptic characteristics of these single crystals used in construction of a Q-switch and a four-crystals modulator are presented. An infrared extension of KURTZ -ROBINSON model electrooptic effect is also given.     

Validation of an LC-MS/MS method for the quantitative determination of mavoglurant (AFQ056) in human plasma

A simple, sensitive, and selective liquid chromatography/tandem mass spectrometry method was validated for the identification and quantification of mavoglurant (AFQ056) in human plasma. The chromatographic separation was performed using a Cosmosil 5 C18 (150?×?4.6 mm, 5 μm) column at 40?±?0.5 °C with a mobile phase consisting of acetic acid in water (0.1 %, v/v)/methanol (10:90, v/v) with a flow rate of 1.0 mL/min followed by quantification with tandem mass spectrometry, operating with electrospray ionization in positive ion mode and applying multiple reaction monitoring. The validated method described in this paper presents high absolute recovery with precision and accuracy meeting the acceptance criteria. The method was precise and accurate for 2- and 10-fold dilution of samples. The method was validated using sodium heparin as specific anticoagulant, and the anticoagulant effect was tested by lithium heparin and K₃EDTA. The method was successfully cross-validated between two bioanalytical sites. The method was specific for mavoglurant within the given criteria for acceptance (apparent peak area at the retention time of mavoglurant in zero samples was less than 20 % compared with the mean peak area at LLOQ) in human plasma. The method was fully validated for the quantitative determination of mavoglurant in human plasma between the range of 2.00 and 2,500 ng/mL.