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Biomedical subjects

R M Barkley

Publications and source records attributed to R M Barkley.

10 recordsLinked to original sources
PubMed1998

Solid-phase microextraction with temperature-programmed desorption for the analysis of iodination disinfection byproducts.

An analytical approach for the determination of chlorination and iodination disinfection byproducts based on solid-phase microextraction (SPME) was developed. Solid-phase microextraction presents a simple, rapid, sensitive, and solvent-free approach to sample preparation in which analytes in either air or water matrixes are extracted into the polymeric coating of an optical fiber. Analytes are subsequently thermally desorbed in the injection port of a gas chromatograph for separation, detection, and quantitation. Thermal degradation of iodoform was observed during desorption from a polyacrylate fiber in initial GC/MS and GC/ECD experiments. Experiments were designed to determine SPME conditions that would allow quantification without significant degradation of analytes. Isothermal and temperature-programmed thermal desorptions were evaluated for efficacy in transferring analytes with wide-ranging volatilities and thermal stabilities into chromatographic analysis columns. A temperature-programmed desorption (TPD) (120-200 degrees C at 5 degrees C/min with an on-column injection port or 150-200 degrees C at 25 degrees C/min with a split/splitless injection port) was able to efficiently remove analytes with wide-ranging volatilities without causing thermal degradation. The SPME-TPD method was linear over 2-3 orders of magnitude with an electron capture detector and detection limits were in the submicrogram per liter range. Precision and detection limits for selected trihalomethanes were comparable to those of EPA method 551. Extraction efficiencies were not affected by the presence of 10 mg/L soap, 15 mg/L sodium iodide, and 6000 mg/L sodium thiosulfate. The SPME-TPD technique was applied to the determination of iodination disinfection byproducts from individual precursor compounds using GC/MS and to the quantitation of iodoform at trace levels in a water recycle system using GC/ECD.

Disinfectants↗
PubMed1995

Aqueous nitrite ion determination by selective reduction and gas phase nitric oxide chemiluminescence.

An improved method of flow injection analysis for aqueous nitrite ion exploits the sensitivity and selectivity of the nitric oxide (NO) chemilluminescence detector. Trace analysis of nitrite ion in a small sample (5-160 microL) is accomplished by conversion of nitrite ion to NO by aqueous iodide in acid. The resulting NO is transported to the gas phase through a semipermeable membrane and subsequently detected by monitoring the photoemission of the reaction between NO and ozone (O3). Chemiluminescence detection is selective for measurement of NO, and, since the detection occurs in the gas-phase, neither sample coloration nor turbidity interfere. The detection limit for a 100-microL sample is 0.04 ppb of nitrite ion. The precision at the 10 ppb level is 2% relative standard deviation, and 60-180 samples can be analyzed per hour. Samples of human saliva and food extracts were analyzed; the results from a standard colorimetric measurement are compared with those from the new chemiluminescence method in order to further validate the latter method. A high degree of selectivity is obtained due to the three discriminating steps in the process: (1) the nitrite ion to NO conversion conditions are virtually specific for nitrite ion, (2) only volatile products of the conversion will be swept to the gas phase (avoiding turbidity or color in spectrophotometric methods), and (3) the NO chemiluminescence detector selectively detects the emission from the NO + O3 reaction. The method is free of interferences, offers detection limits of low parts per billion of nitrite ion, and allows the analysis of up to 180 microL-sized samples per hour, with little sample preparation and no chromatographic separation. Much smaller samples can be analyzed by this method than in previously reported batch analysis methods, which typically require 5 mL or more of sample and often need chromatographic separations as well.

Colorimetry↗
PubMed1987

Gas chromatographic measurement of carbon monoxide in hydrocarbon matrices with a redox chemiluminescence detector.

The rapid measurement of trace levels of carbon monoxide in ethylene by gas chromatography with redox chemiluminescence detection is described. Linear response for carbon monoxide over three decades and a detection limit in the sub-parts per million by volume (ppmv) concentration range were observed without methanation or preconcentration of the sample. Samples containing 0.2 ppmv of carbon monoxide in ethylene were readily quantitated.

Carbon Monoxide↗
PubMed1984

Chromatographic analysis of organic compounds in the atmosphere.

Fused silica capillary columns with thick films of cross-linked coatings have been used to separate many of the organic compounds that are present in the volatile fraction of automobile exhaust and in ambient air. Techniques have been developed that allow reversible collection and pre-concentration of organic compounds in ambient air on polymeric sorbents with minimal artifacts. The exhaust samples, which are directly injected without pre-concentration on sorbents, contain many of the same organic compounds that are found in sorbent-collected samples of urban ambient air. Similar anthropogenic organic compounds are not, in general, detected (less than 0.02 ppbV) in air samples from remote, rural areas in Colorado.

Air↗
PubMed1984

Aminomalonic acid: identification in Escherichia coli and atherosclerotic plaque.

Aminomalonic acid (Ama) has been isolated from proteins of Escherichia coli and human atherosclerotic plaque. The presence of Ama has important biological implications because the malonic acid moiety potentially imparts calcium binding properties to protein. Ama was obtained by anaerobic alkaline hydrolysis and identified by chromatographic behavior, quantitative acid-mediated decarboxylation to glycine, and unambiguous gas chromatographic/mass spectral detection. The chromatographic, chemical, and mass spectral properties of naturally occurring Ama were identical to those of the synthetic compound. Amino acid analysis and GC/mass spectrometry also revealed the presence of beta-carboxyaspartic acid and gamma-carboxyglutamic acid in the base hydrolysate of human atherosclerotic plaque. The ratio of Ama to beta-carboxyaspartic acid to gamma-carboxyglutamic acid was 20:1:10, and the quantity of Ama per 1,000 glycine residues was 0.2. Ama is a relatively unstable, minor amino acid in complex structures such as bacteria or tissues. This may explain why it has escaped detection previously, despite intensive investigation.

Amino Acids↗
PubMed1979

Spontaneous secretion from the dog small intestine in vivo.

Forty loops of small intestine in the dog were perfused under control conditions with a balanced electrolyte solution. Most of the loops absorbed sodium and water, but 10 loops were in a state of spontaneous intestinal secretion. Compared to absorbing loops, spontaneously secreting loops exhibited reduced values for lumen-to-plasma fluxes of sodium and chloride and increased values for the plasma-to-lumen fluxes of these ions. Analysis of flux ratios suggested that sodium and chloride were actively scecreted during spontaneous intestinal secretion in the dog. Spontaneous secretion was similar to the secretion induced by CT or VIP, except that the latter were associated with a change in PD whereas the PD in the spontaneously secreting loops was the same as in the spontaneously absorbing loops.

Animals↗
PubMed1978

Intestinal secretion induced by vasoactive intestinal polypeptide. A comparison with cholera toxin in the canine jejunum in vivo.

The effect of vasoactive intestinal polypeptide (VIP) on intestinal water and electrolyte transport and transmucosal potential difference was investigated in the dog jejunum in vivo and compared to secretion induced by cholera toxin. Isolated jejunal loops were perfused with a plasma-like electrolyte solution. VIP (0.08 mug/kg per min) was administered directly into the superior mesenteric artery by continuous infusion over 1 h. From a dye dilution method, it was estimated that a mean plasma VIP concentration of 12,460 pg/ml reached the loops. VIP caused secretion of water and electrolytes; for example, chloride: control, 8 mueq/cm per h absorption; VIP, 92 mueq/cm per h secretion. A marked increase in transmucosal potential difference (control, -1.0 mV; VIP, -5.9 mV, lumen negative) occurred within 1 min after starting VIP infusion. Analysis of unidirectional fluxes showed increased plasma-to-lumen flux of sodium and chloride and decreased lumen-to-plasma flux of sodium. Chloride and bicarbonate were actively secreted against an electrochemical gradient. Although sodium secretion occurred down an electrochemical gradient, flux ratio analysis suggested a component of active sodium secretion. VIP caused a slight increase in protein output into the loops; light microscopy revealed capillary dilatation and closed intercellular spaces. The effect of VIP was readily reversible. Except for the delayed onset of secretion, the effect of cholera toxin was qualitatively similar to VIP; however, capillary dilatation and increased protein output were not noted with cholera toxin.

Animals↗
PubMed1977

Environmental trace analysis of organics in water by glass capillary column chromatography and ancillary techniques. Products of ozonolysis.

A method employing a polymeric sorbent has been used for analysis of volatile organic components in water. Trace level organics are sparged from water with nitrogen gas and are concentrated on Tenax GC prior to analysis with either flame ionization gas chromatography or gas chromatography-mass spectrometry. Glass capillary columns were used to obtain maximum resolution of chromatographic peaks. Specifically, the method has been applied to a qualitative and quantitative study of the products which result from ozonization of secondary treated domestic wastewater. The principal volatile products of ozonolysis are n-hexanal, n-heptanal, n-octanal and n-nonanal. Representative samples contained 0.7 ppb** of n-heptanal and less than 1 ppb of any of the volatile compounds.

Chromatography, Gas↗