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Biomedical subjects

R A Hites

Publications and source records attributed to R A Hites.

34 records · Page 2Linked to original sources

Organic compounds near dumpsites in Niagara Falls, New York.

Water and sediment samples were taken from sites adjacent to hazardous waste disposal areas in Niagara Falls, New York. The samples were analyzed by gas chromatographic mass spectrometry. The following compounds were identified: chlorobenzenes, chlorotoluenes, polycyclic aromatic hydrocarbon derivatives, cyclohexane derivatives, polychlorinated biphenyls, trichlorophenol and other phenols, benzotrifluorides, mirex and phenothiazine. A large number of benzyl derivatives and unusual fluorinated compounds were also found; they were probably waste by-products of industrial chemical production. The hazardous waste disposal sites were probably the major sources for most of the compounds.

Gas Chromatography-Mass Spectrometry↗

Mutation of human cells by kerosene soot.

The polycyclic aromatic hydrocarbon fraction of a kerosene soot induced forward mutation in human diploid lymphoblasts when coincubated with Sprague-Dawley rat liver postmitochondrial supernatant. Two components of the kerosene soot extract, benzo[a]pyrene (BP) and cyclopenta[cd]pyrene (CP), were also tested. TP was not mutagenic at the concentration found in the soot extract, although it was active at higher concentrations. The amount of CP present could account for approximately 8% of the total mutation observed with the soot. The results were compared to data obtained previously in a similar mutation assay in Salmonella typhimurium. The protocol described permits the facile assay of mutation at the hgprt locus in human lymphoblasts; such mutation is induced by compounds of complex mixtures requiring mixed-function oxygenase activity for metabolism to genetically active derivatives.

Animals↗

Source identification of urban airborne polycyclic aromatic hydrocarbons by gas chromatographic mass spectrometry and high resolution mass spectrometry.

Polycyclic aromatic hydrocarbons formed during the combustion of three common fuels (coal, wood and kerosene) were separated and identified by capillary-column gas chromatographic mass spectrometry and were compared to airborne polycyclic aromatic hydrocarbons from Indianapolis, a high coal consuming area, and Boston, a low coal consuming area. High resolution mass spectral data were utilized in the construction of alkyl homolog plots for the comparison of alkyl distribution within each sample.

Air Pollution↗

The analysis of organic water pollutants by gas chromatography and gas chromatography-mass spectrometry.

Four methods for the analysis of trace levels or organic compounds in water have been discussed: direct aqueous injection, vapor stripping, solvent extraction, and lipophilic adsorption. Table 6 presents a comparison of these techniques. Direct injection is applicable to compounds having a wide range of polarities and volatilities, but it is not a very sensitive technique. For applications in which low sensitivity is acceptable, direct injection offers a very rapid and potentially accurate means of measuring organics in water. Vapor stripping is a factor of 10(6) more sensitive than direct injection, but this is achieved at the expense of simplicity. This method is applicable to compounds of volatilities less than that of eicosane. A subtle operational problem with most vapor stripping techniques is that the contents of the trap are consumed with one analysis; if anything goes awry, the analysis of that trapped sample cannot be repeated. Solvent extraction has a respectable sensitivity (about 0.5 ppb) and operationally it is very simple. Furthermore, aliquots of the resulting extract can be analyzed many times with different techniques if necessary. Because of the evaporation step, very volatile compounds (greater than that of decane) cannot be measured effectively with solvent extraction. The introduction of a solvent into the water carries with it the potential for contamination. Thus, ultrapure solvents must be used and all glassware should be carefully cleaned [96]. Lipophilic adsorption has the unique property of sampling many hundreds of liters of water. Thus, the method is quite sensitive (potentially in the ppt range) and, in addition, it can provide several milligrams of an isolated component. This latter feature is of considerable advantage if one wants to complement GC-MS analyses with infrared or NMR for difficult structural identifications. As a solvent extraction, the evaporation of the final solvent limits the applicability of adsorption methods to compounds with volatilities greater than that of decane. Finally, the importance of avoiding contamination should be emphasized. Many of the compounds encountered in environmental samples are also common laboratory artifacts, for example plasticizers and antioxidants. When one finds such compounds in a water sample, it is absolutely essential to demonstrate that they are indeed present in the water and are not the result of laboratory contamination. The best such demonstration is procedural blank analyses that are indeed blank.

Chromatography, Gas↗

Water pollution: organic compounds in the Charles River, Boston.

The major lipophilic organic compounds present in water collected during November and December 1971 from the Charles River Basin (Boston) are as follows: normal alkanes (C(15) to C(31)), alkyl naphthalenes, alkyl anthracenes or phenanthrenes, pyrene, fluoranthene, dibutyl phthalate, and di(2-ethylhexyl) phthalate. The concentration of the naphthalenes (determined by liquid chromatography) correlates with the effective storm-water runoff content of the river. These data suggest a multiplicity of sources ranging from indigenous biological materials to automobile exhaust condensate.

Alkanes↗