Design Features of a High Resolution Microcalorimeter EDX System

 High resolution, superconducting detectors allow energy dispersive X-ray spectrometry (EDX) with energy resolution and energy threshold far beyond the levels obtained with semiconductor detectors. These cryogenic detectors are run at temperatures of less than 100 mK and combine the excellent energy resolution of wavelength dispersive X-ray spectrometry (WDX) with the fast, energy dispersive analysis of EDX. CSP cryogenic spectrometer’s microcalorimeter type EDX cryodetectors are equipped with a mechanical cooling system that runs vibration free and allows completely automated operations on scanning electron microscopes (SEMs), field emission guns (FEGs) and transmission electron microscopes (TEMs). This detector type offers new opportunities in material analysis, especially when low excitation energies are applied or light elements are to be determined.     

General collective model and its application to 92 238 U

A general collective model is presented that includes all possible cases, like vibrational, rotational andγ-unstable nuclei. Collective properties are illustrated by the Potential-Energy-Surface (PES), describing all deformation effects of the nucleus. The model is applied to the case of ₉₂ ²³⁸ U, where very high-spin states are known from experiment.     

High-throughput analysis of telomerase by capillary electrophoresis

The enzyme telomerase is expressed in (85-90)% of all human cancers, but not in normal, non-stem cell somatic tissues. Clinical assays for telomerase in easily obtained body fluids would have great utility as noninvasive, cost-effective methods for the early detection of cancer. The most commonly used method for the detection and quantification of telomerase enzyme activity is the polymerase chain reaction (PCR)-based assay known as the telomerase repeat amplification protocol or TRAP assay. Most of the TRAP assay systems use a slab-gel based electrophoresis system to size and quantify the PCR-amplified extension products. We are developing high-throughput capillary electrophoresis (CE) methods for the analysis of TRAP/PCR products. The TRAP assay was conducted on lysates of the human lung cancer cell line A-549 in reactions containing 5-100 cells. TRAP/PCR products were generated using a fluorescent 4,7,2'4'5'7',-hexachloro-6-carboxyfluorescein(HEX)-labeled TS primer and analyzed on the Applied Biosystems Model 310 CE system using POP4 polymer. After analysis with GeneScan and Genotyper software, the total peak areas of the TRAP ladder extension products were computed using Microsoft Excel. Results were compared with unlabeled TRAP/PCR products analyzed on the Bio-Rad BioFocus 3000 CE system using 6% high molecular weight polyvinylpyrrolidone (HMW PVP) polymer and SYBR Green I dye. Both CE systems were able to resolve the TRAP ladder products with high reproducibility and sensitivity (5-15 cells). With the appropriate robotic sample handling system, these CE methods would enable performing the telomerase TRAP assay with increased sensitivity, reproducibility and automation over slab-gel methods.     

Die polarographische Bestimmung von l-Ascorbins?ure im Wein

Zusammenfassung Unter Berücksichtigung des Einflusses von Sauerstoff, freier schwefliger Säure und Äthanol wird eine geeignete Methode zur polarographischen Bestimmung von Ascorbinsäure in Wein angegeben.Für die Untersuchungen wurden Mittel des Bundesernährungs-Ministeriums zur Verfügung gestellt, wofür auch an dieser Stelle bestens gedankt sei.Die Arbeit stellt einen Ausschnitt dar aus der Dissertation von D. Hess: Über den Einfluß von schwefliger Säure und l-Ascorbinsäure bei der Weinbereitung (Universität Frankfurt am Main 1960).     

Excimer laser spectroscopy: influence of tissue ablation on vessel wall fluorescence

Limited steerability and injury to the normal vessel wall are major drawbacks of laser coronary angioplasty. To overcome these limitations a new generation of laser systems has been developed which allows not only to eliminate the atherosclerotic plaque but to guide the laser beam by analyzing the laser induced tissue fluorescence (= spectroscopy) for the treatment of the atherosclerotic vessel. An excimer laser (MAX 10 LP, 308 nm, Technolas, Munich, Germany) was used with an emitting (phi 1070 microns) and a detecting (phi 130 microns) optical fiber to induce tissue fluorescence which was analyzed quantitatively by a computerized system. Specimens from the descending (thoracic) aorta were obtained from 24 patients (mean age 68.1 years, range 44-92). Tissue fluorescence was induced with ablating (26-30 mJ/mm2) and nonablating (3 mJ/cm2) laser activations. The emitted fluorescence (range 380-575 nm) was normalized to a wavelength of 380 nm; as a measure of tissue fluorescence the intensity ratio at 500 nm divided by 400 nm was calculated in normal (n = 78), mildly atherosclerotic (n = 40), and severely atherosclerotic (n = 48) tissue samples. Repeated laser activations were carried out and tissue fluorescence was checked until the fluorescence spectrum was normalized. All tissue samples were analyzed histologically by a semiquantitative score. Normal tissue samples showed the highest intensity ratios (5.9 +/- 3.4), whereas mildly (2.9 +/- 1.3) and severely atherosclerotic (2.1 +/- 1.0) samples elicited a significantly reduced fluorescence. Repeated tissue ablations were associated with a normalization of fluorescence intensity ratios in the mildly (7.0) as well as in the severely diseased (4.9) vessels. A curvilinear relationship between intensity ratio and the semiquantitative score was observed (r = 0.66) as well as between intensity ratio and intimal wall thickness (r = 0.62). No gender related differences were found but there was an inverse relationship between fluorescence intensity ratio and age (r = 0.56) as well as between intimal thickness and age (r = 0.41). Excimer laser spectroscopy allows reliable detection of atherosclerotic vessel alterations. Fluorescence intensity ratio is inversely proportional to the intimal wall thickness and the severity of the histologic alterations. There is an age dependency of fluorescence intensity ratio which can be explained by an increase in intimal wall thickness. Successful tissue ablation can be obtained by laser angioplasty and allows determination of the optimal point where complete tissue ablation is achieved by laser activation. Thus, excimer laser spectroscopy is an effective method for selective tissue ablation by laser angioplasty.