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Biomedical subjects

M Novotny

Publications and source records attributed to M Novotny.

At least 91 records · Page 5Linked to original sources

Structural relationships between the endogenous volatile urinary metabolites of experimentally diabetic rats and certain neurotoxins (l).

High resolution glass capillary gas chromatography and GC/MS were utilized to examine qualitative and quantitative variations from normal of urinary volatile metabolites of long-term alloxan and streptozotocin diabetic rats. Volatile metabolites were structurally compared with known neurotoxins to examine any possible relationship between these metabolites and the development of the diabetic polyneuropathy.

Animals↗

Recent advances in capillary gas chromatography related to drug research.

Recent progress in capillary gas chromatography, with emphasis on the needs of drug research, has been briefly reviewed. The value of this method in studies of drug-induced changes in metabolic profiles has been emphasized. Recent improvements in technology of glass and fused-silica capillary columns and enhanced capabilities of detectors related to capillary techniques promise to increase their utilization in drug research and routine analyses.

Animals↗

Metabolic abnormalities associated with diabetes mellitus, as investigated by gas chromatography and pattern-recognition analysis of profiles of volatile metabolites.

Patterns of volatile metabolites in urine, as obtained by glass-capillary gas chromatography, were investigated by use of a nonparametric pattern-recognition method, in an effort to detect abnormalities associated with diabetes. We used threshold logic unit analysis on a data set consisting of normal subjects and those with diabetes mellitus, and could predict patterns for volatile metabolites as belonging to the proper class in 94.83% of the cases examined. In addition, a feature-extraction algorithm isolated those volatile constituents that are most useful in making the normal/diabetic classification. We used gas chromatography/mass spectrometry to identify important profile constituents. Finally, these same pattern-recognition methods indicated strong sex-related patterns in these volatiles.

Chromatography, Gas↗

Gas-chromatographic determination of polyol profiles in cerebrospinal fluid.

We describe a simple method for collectively determining polyols in the cerebrospinal fluid. The method consists of protein removal, sample derivatization, and gas chromatography of the trimethylsilylated polyols, with use of glass capillary columns. Nine major polyol constituents, the structures of which were verified by combined gas chromatography/mass spectrometry, can be simultaneously assayed. The presence of three polyols in the cerebrospinal fluid is reported here for the first time.

Chromatography, Gas↗

Use of a modified Tenax GC column packing for the direct gas chromatographic analysis of phenols in water at the ppm level.

Dilute solutions of phenols in water at the ppm level may be analysed gas chromatographically by direct injection onto a column with a packing similar to that used in the Viking 1975 spacecraft: Tenax GC (2,6-diphenyl-p-phenylene oxide polymer) modified with polymetaphenyl ether liquid phase to eradicate irreversible adsorption. Symmetrical peaks were observed for injections of less than 1 ng of phenol and some of its alkylated derivatives. Chromatographic properties of modified Tenax GC columns are reported along with their application to the analysis of some industrial effluents with previous work-up.

Chromatography, Gas↗

Time constant of thermistors and its role in thermodilution methods.

Thermolution serves for measuring either the cardiac output or the size of cardiac ventricles. In the former instance, an accurate determination of the area under the dilution curve, and in the latter, a true tracing of the thermal changes with time are of special importance. Because the size of the area is independent of the time constant, and a curve devoid of marked stroke waves is better suited for automatic integration, thermistors with time constants of 0.8 to 1.0 sec are chosen for this purpose. A reliable determination of the time constant is described. In measurements of the size of cardiac ventricles, a true course of thermal changes with time can be recorded with a thermistor possessing a very short time constant: 0.01 to 0.02 seconds. It is very difficult to make such thermistorized probes or catheters. It is easier to make thermistors with a time constant of 0.1 o 0.2 sec, well insulated, which may serve both requirements. By compensation, the time constant is reducible to 0.01 to 0.2 sec, making possible a true-shape recording of thermal changes for the measurement of the ventricular size, or the constant can be prolonged to 0.8 to 1.0 sec for instrumental integration. If both the shape and the time course of the thermal changes have to be truly recorded, then a non-insulated thermistor with a very short time constant has to be used.

Blood Volume↗