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PubMed2005

Pilot study of a breath test for volatile organic compounds associated with oral malodor: evidence for the role of oxidative stress.

BACKGROUND: We performed a pilot study of a new method to identify the volatile organic compounds (VOCs) in breath associated with oral malodor, using gas chromatography and mass spectroscopy (GC/MS). METHODS: Oral cavity breath was collected from seven patients with oral malodor. Breath samples (150 ml) were concentrated onto sorbent traps and analyzed by GC/MS. RESULTS: Organoleptic scores ranged from 3.0 to 4.0 (mean = 3.3) on a scale of 0-5. Twenty-four of 30 (80.0%) of the most abundant oral malodor volatile organic compounds (OMVOCs) were alkanes and methylated alkanes. These VOCs are products of oxidative stress, generated by lipid peroxidation of polyunsaturated fatty acids in cell membranes. CONCLUSIONS: Increased oxidative stress in the oral cavity of patients with oral malodor may account for the increased risk of atherosclerosis, coronary heart disease and stroke associated with periodontal disease. The breath test for OMVOCs could potentially provide an objective new test for the assessment of oral malodor.

Alkanes↗

PubMed1997

[Analysis of semi-volatile organic compounds in chemical waste by gas chromatography/mass spectrometry].

According to US EPA 8270 method the semi-volatile organic compounds in chemical waste were analysed by internal standard method which could eliminate the systematic and injection errors and increase the accuracy of the results. Through this experiment, ten prior pollutants of US EPA and eleven organic chlorinated compounds with concentrations between 0.4 microg/g and 80 microg/g in the waste were determined. It is concluded that the waste was hazardous and could not be disposed without proper treatment.

Gas Chromatography-Mass Spectrometry↗

PubMed2002

Soil-water partitioning and desorption hysteresis of volatile organic compounds from a Louisiana Superfund site soil.

The adsorption and desorption of three volatile organic compounds (1,2-dichloroethane, 1,1,2- trichloroethane and 1,1,2,2-tetrachloroethane) from a previously uncontaminated clayey soil sample from a Superfund site in North Baton Rouge, Louisiana was studied. In the linear range of the adsorption isotherm, the partition constants were not affected by the presence of the co-solutes. The adsorption isotherms over a wide concentration range on the soil followed the nonlinear Freundlich isotherm. The desorption of the compounds showed significant hysteresis at all concentrations studied. Approximately 20 to 70% of the adsorbed mass of organic compounds resisted the desorption even after five months of successive desorption steps. The desorption of four compounds (1,2-dichloroethane, 1,1,2-trichloroethane, 1,4-dichlorobenzene and hexachlorobutadiene) from a contaminated soil sample from the same site was also studied. The aqueous concentration declined as the successive desorption steps progressed. For hexachlorobutediene the desorption can be visualized as occurring in two stages. The first stage involved a 'loosely bound' or 'reversible' fraction and the second stage involved a 'tightly bound' or 'resistant' fraction.

Adsorption↗

PubMed1995

Evaluation of the allergic/irritant potential of air pollutants: detection of proteins modified by volatile organic compounds from oilseed rape (Brassica napus ssp. oleifera) using electrospray ionization-mass spectrometry.

BACKGROUND: Upward trends in allergy and asthma rates have been reported in most western societies, including the UK, where around 15-20% of the population now suffer from allergy or asthma. Scientific proof of the causes of these increases relies on accurate assessment of exposure and standardized diagnostic tests, such as for specific IgE in blood serum and skin testing. For many air pollutants it has proven difficult to assess an individual's exposure outside an occupational environment and reliable test development is hampered by not knowing whether an allergic or irritant mechanism is involved. These problems are particularly evident in the controversial issue of whether airborne releases from oilseed rape can cause health effects. OBJECTIVE: To develop a method for evaluating the allergic/irritant potential of air pollutants and to assess whether the volatile organic compounds emitted by oilseed rape have this potential. METHODS: Proteins were exposed in vitro to volatile organic compounds emitted by oilseed rape. Electrospray ionization-mass spectrometry was used to detect any resultant protein modifications. RESULTS: Dimethyl disulphide, thiocyanic acid methyl ester and 2-methyl-propanenitrile were able to modify human proteins. In addition, two isothiocyanates which can be emitted by damaged oilseed rape also have this ability. The major products emitted by undamaged oilseed rape, terpenes, a sesquiterpene and a terpene alcohol did not have this property, but the possible role of their oxidized products is discussed. CONCLUSION: Some of the volatile organic compounds emitted by oilseed rape have the potential to be allergens/irritants. Standardized modified proteins produced by this method should prove useful for biomonitoring human exposure in molecular epidemiological studies as well as in diagnostic tests. This method should find further application in investigations into the possible health effects of other environmental pollutants.

Air Pollutants↗

PubMed2000

[Determination of volatile organic compounds in blood by headspace solid-phase microextraction-gas chromatography].

The headspace solid-phase microextraction (HS-SPME) is a novel extraction technique and has been developed rapidly. It is a fast, simple, solventless and sensitive method for sampling, separating, extracting, injecting and analyzing volatile organic compounds. This paper presents the research work in detecting volatile organic compounds(including ten compounds) in blood. The extraction fiber is made by fused-silica fiber with 100 microns polydimethylsiloxane (PDMS). The extraction time of the method was 10 min. The thermal desorption time was 1 min. It was found that the optimized location of the extraction fiber in the injector of GC was to put the whole needle in the injector. The precision of the method was determined to be less 5% relative standard deviation (RSD). The linear range of the detection was rather wide. The lowest detectin limits (LODs) were all < or = 5 ng/ml.

Animals↗

PubMed2003

A screening assessment of emissions of volatile organic compounds and particles from heated indoor dust samples.

This paper characterizes and compares emissions during heating of different dust samples relevant to the indoor environment. Characterization includes emission of volatile organic compounds when dust samples were heated to 150 and 250 degrees C (gas chromatograph-mass spectrometer), weight loss during heating to 450 degrees C (thermogravimetric analysis), and the number of particles emitted during heating towards 200 degrees C (condensation nucleus counting). Element analyses were performed for non-heated dust (inductively coupled plasma discharge instrument). Emissions of volatile organic compounds from heated dust from different sources were surprisingly similar. However, the temperature at which the emission of volatiles started varied with the dust source. For most of the samples studied, the emissions were considerable already at 150 degrees C, and increased in number of peaks and peak area at 250 degrees C. Particle emissions started around 70 degrees C regardless of the dust source. Particle emissions seemed to be affected by the content of organic material.

Air Pollutants↗

PubMed2004

Determination of volatile organic compounds in workplace air by multisorbent adsorption/thermal desorption-GC/MS.

Investigation of volatile organic compounds (VOCs) was first conducted in the air of class-100 cleanrooms at liquid crystal display (LCD) fabrication facilities. Air samples were collected on multisorbent tubes (including Carbopack B, Carbopack C, and Carbosieve S-III) and analyzed using adsorption/thermal desorption coupled with gas chromatography-mass spectrometry (GC-MS). Optimal conditions lead to average recoveries in the range of 96.2-98.2%, and method detection limits between 0.38 and 0.78 ppb, under the condition of 1-l sampling volume and 80% relative humidity. The method appears to be accurate, sensitive, simple and well-suited for determining VOC distributions from various stages of LCD manufacturing process and temporal variations of the analyte concentrations. About 15 VOCs were identified in workplace air. The major pollutants such as propylene glycol methyl ether acetate (PGMEA), butyl acetate, and acetone that are commonly used in the opto-electronics industry were detected and accurately quantified with the established method.

Adsorption↗

PubMed2001

Detection of microbial volatile organic compounds (MVOCs) produced by moulds on various materials.

Twelve fungal species were screened for microbial volatile organic compounds (MVOCs): Aspergillus fumigatus, A. versicolor, A. niger, A. ochraceus, Trichoderma harzianum, T. pseudokoningii, Penicillium brevicompactum, P. chrysogenum, P. claviforme, P. expansum, Fusarium solani and Mucor sp. More than 150 volatile substances derived from fungal cultures have been analysed by head-space solid-phase microextraction (HS-SPME). Each species had a defined MVOC profile which may be subjected to considerable modification in response to external factors such as cultivation on different substrata. The cultivation on different substrata changes the number and concentration of MVOCs. Species-specific volatiles may serve as marker compounds for the selective detection of fungal species in indoor environments. Examination of MVOCs from indoor air samples may become an important method in indoor air hygiene for the detection of type and intensity of masked contamination by moulds.

Air Pollution, Indoor↗

PubMed2006

Volatile organic compounds in the exhaled breath of young patients with cystic fibrosis.

Inflammatory mediators in the exhaled breath are receiving growing medical interest as noninvasive disease markers. Volatile organic compounds have been investigated in this context, but clinical information and methodological standards are limited. The levels of ethane, propane, n-pentane, methanol, ethanol, 2-propanol, acetone, isoprene, benzene, toluene, dimethyl sulphide (DMS) and limonene were measured in repeated breath samples from 20 cystic fibrosis patients and 20 healthy controls (aged 8-29 yrs). Three end-exhaled and one ambient air sample were collected per person and analysed on a customised gas chromatography system. Intra-subject coefficients of variation ranged between 9 and 34%, and hydrocarbon breath levels were influenced by their inspired concentrations. The alveolar gradient for pentane was higher in cystic fibrosis patients than in healthy controls (0.36 versus 0.21 ppb) and inversely proportional to forced expiratory volume in one second; highest values were observed in patients with pulmonary exacerbations (0.73 versus 0.24 ppb). Cystic fibrosis patients also exhibited a lower output of DMS (3.9 versus 7.6 ppb). Group differences were not significant for ethane and the remaining substances. It was concluded that chemical breath analysis for volatile organic compounds is feasible and may hold potential for the noninvasive diagnosis and follow-up of inflammatory processes in cystic fibrosis lung disease.

2-Propanol↗

PubMedDate not supplied

Interim method for determination of volatile organic compounds in hazardous wastes.

An analytical protocol is presented for the determination of volatile organic compounds in hazardous wastes that are amenable to the purge-and-trap method. The protocol features a tetraethylene glycol dimethyl ether (tetraglyme) extraction of the liquid or solid waste, addition of an aliquot of the tetraglyme waste to water, and purging of the tetraglyme-water mixture with subsequent gas chromatographic/mass spectrometric (GC/MS) analysis. The size of the tetraglyme aliquot is determined by gas chromatographic screening of a hexadecane waste extract. Quality assurance/quality control procedures are included within the analytical protocol. Spike extraction recoveries of industrial wastes obtained by following this protocol are given.

Carcinogens↗

PubMed1998

Role of kinetics in acute lethality of nonreactive volatile organic compounds (VOCs).

The role of kinetics in the acute inhalation toxicity of nonreactive, volatile organic compounds (VOCs), including lipophilic and hydrophilic compounds, was analyzed with a physiologically based pharmacokinetic (PB-PK) model for the rat. For 15 VOCs, a total of 23 LC50 values were retrieved from the literature. It was observed that the external exposure parameter (LC50.exposure length; in ppm.h), varied approximately 60-fold. Concentrations of compounds in the lipoid brain fraction were simulated using a kinetic model. This lead to a more than 10-fold reduction in the toxic range of the 15 VOCs. The average value for this simulated dose surrogate was 70 +/- 31 mM for all VOCs. These observations support the presumption that nonspecific, acute narcotic lethality is directly related to the extent of VOC distribution into lipoid brain constituents. The present results can be used for estimation of the acute lethality of nonreactive VOCs on the basis of kinetic simulations. In addition, the presently calculated dose surrogate for VOC lethality in rats is found to be very similar to the reported internal lethal concentrations of so-called "baseline toxicity compounds" in fish. This indicates a common mechanism of acute VOC toxicity among mammalian and aquatic species.

Alkanes↗

PubMed2005

Priority volatile organic compounds in surface waters of the southern North Sea.

The occurrence of 25 volatile organic compounds (VOCs) was studied from April 1998 to October 2000 in the southern North Sea. Target VOCs were selected from lists of priority pollutants for the marine environment and included, e.g., chlorinated short-chain hydrocarbons (CHCs), monocyclic aromatic hydrocarbons (MAHs), and chlorinated monocyclic aromatic hydrocarbons (CMAHs). Water samples were taken from the Channel, the Belgian Continental Shelf, the mouth of the Scheldt estuary and the Southern Bight, and were analysed by purge-and-trap and high-resolution gas chromatography-mass spectrometry. All data were produced by analyses deemed 'in control' by a rigorous quality assurance/quality control program provided by QUASIMEME (Quality Assurance of Information for Marine Environmental Monitoring in Europe). Chloroform and trichloroethene were commonly detected at concentrations up to 1900 and 270 ng l(-1), respectively. The other CHCs were generally found below 5 ng l(-1), and rarely exceeded 10 ng l(-1). Concentrations of MAHs were at least one order of magnitude higher than those of the CHCs. The higher levels were attributed to anthropogenic emissions from oil-related activities in coastal areas. CMAHs, except chlorobenzene and 1,4-dichlorobenzene, were hardly detected in North Sea waters. The levels of several CHCs and MAHs were shown to decrease compared to previous investigations in 1994-1995, probably as a result of on-going emission reduction efforts. The occurrence of 1,1,1-trichloroethane, for instance, was substantially reduced since the Montreal Protocol was implemented in 1995.

Chloroform↗

PubMed2003

Analysis of volatile organic compounds in air with a micro ion trap mass analyzer.

Analysis of several volatile organic compounds in air has been demonstrated with a micro ion trap mass analyzer equipped with a semipermeable membrane sampling inlet. MS/MS of selected compounds was also shown to be feasible with the miniature ion trap and could be used to improve sensitivity by reducing background noise.

Journal Article↗

PubMedDate not supplied

A canister-based method for collection and GC/MS analysis of volatile organic compounds in human breath.

A method previously used for collection and analysis of volatile organic compounds (VOCs) in human whole breath was modified to encompass compounds with higher vapor pressures. A VOC spirometer was designed for field studies of environmentally exposed populations with breath concentrations in the microgram/m3 (ppb) range. The VOC spirometer was configured for sample collection and GC/MS analysis of breath samples using stainless steel canisters. Recoveries of 17 analytes in synthetic breath through the spirometer at 4 and 21 degrees C were generally above 80% except for n-dodecane which demonstrated poor recoveries at the lower temperature. The maximum sample volume available for analysis during recovery studies with natural breath was 100 mL because of copious quantities of CO2 present. Decay curves showing the breath elimination of 1,1,1-trichloroethane and benzene from a man after exposure to consumer products demonstrates the utility of the method.

Breath Tests↗

PubMed2005

An infrared evanescent wave sensing system coupled with a hollow fiber membrane for detection of volatile organic compounds in aqueous solutions.

We have developed an on-line sensing method for the detection of volatile organic compounds (VOCs) in contaminated aqueous solutions by combining a microporous hollow fiber membrane with an infrared (IR) sensing system. Polypropylene microporous hollow fibers were used to separate the VOCs from the aqueous solution into the hollow fibers, which were purged countercurrently for detection by the IR sensing systems. An evanescent-wave-type IR sensing system was used to detect the VOCs that were purged from the hollow fibers. The sensing element was coated with polyisobutylene (PIB) to concentrate the VOCs for their detection. To study the performance of this system, we examined a number of factors, such as the purging flow rate, the sample flow rate, and the volatilities of the VOCs. The results indicate that an increase in the purging flow rate reduces the analytical signal significantly, especially for purging flow rates >2 mL/min. The pumping flow rate for the aqueous sample also influenced the analytical signals, but far less sensitively. The volatilities of the examined compounds also affected the analytical signals: the higher the volatility of the compound, the lower the intensity of the analytical signals and the shorter the time required to reach the equilibrium signal. From an examination of the dynamic range of this proposed method, a regression coefficient >0.994 was obtained for concentrations below 250 mg/L, even under non-equilibrium conditions. The response time of the system was studied in an effort to examine the suitability of using this sensing method for automatic detection. The results indicate that new equilibrium conditions were established within 3 min for highly volatile compounds, which suggests that on-line monitoring of the levels of VOCs can be performed in the field.

Membranes, Artificial↗

PubMed2004

A simple model for estimating emissions of volatile organic compounds from grass and cut grass in urban airsheds and its application to two Australian cities.

Grass, and particularly cut grass, recently has been shown to emit significant amounts of volatile organic compounds (VOCs) into the atmosphere. Some components of these emissions are highly reactive and may contribute to photochemical smog in urban areas. A simple model for estimating the VOC emissions from grass and for grass cutting that allows these processes to be included in urban/regional emissions inventories is presented here. Using previous work and recent literature values, estimates are made of these biogenic volatile organic compound (BVOC) emissions for two typical urban airsheds, those including the cities of Sydney and Melbourne in Australia. Grass and cut grass could contribute approximately 2% for Sydney and 3% for Melbourne of the total VOCs emitted into these urban atmospheres annually. These contributions could rise to 4 and 5%, respectively, during the weekends of the summer growing season and, thus, could contribute to weekday/weekend ozone differences. It is recommended that the emissions of BVOCs from grass and cut grass be included in urban and global emissions inventories so that more accurate predictions of smog chemistry can be determined.

Australia↗

PubMed2000

Analysis of volatile organic compounds, using the purge and trap injector coupled to a gas chromatograph/ion-trap mass spectrometer: review of the results in Dutch surface water of the Rhine, Meuse, Northern Delta Area and Westerscheldt, over the period 1992-1997.

Volatile organic compounds are widely introduced into the Dutch aquatic environment. Liquid-liquid extraction and isolation by means of resins give poor recoveries for volatiles. In this study, a method has been developed to analyse these compounds with a purge and trap injection (PTI) coupled to a chromatograph/ion trap mass spectrometer. Volatile compounds are "purged" from the sample by carrier gas flow and transported through a condenser to a cooled trap. The bulk of liquid matrix is condensed in the condenser, while volatile compounds are left unaffected. The compounds of interest are trapped at a low temperature, by liquid nitrogen in the cooled trap of fused silica. Injection takes place by flash heating of the trap. The detection limits of the volatile compounds are in the range of 0.001-0.04 microgram l-1, in full spectrum mode. In this paper a review of the results in Dutch surface water of the Rhine, Meuse, Northern Delta Area and Westerscheldt, over the period 1992-1997, is presented. For calamities causing high levels of volatiles, the method is very useful. The compounds can be monitored over a certain period. In the Meuse, high levels of volatile organic compounds are observed. Diisopropyl ether at a maximum of 592 micrograms l-1.

Chlorobenzenes↗

PubMed2004

Screening processed milk for volatile organic compounds using vacuum distillation/gas chromatography/mass spectrometry.

An adaptation is presented of method 8261--from the Office of Solid Waste and Emergency Response Test Methods for Evaluating Solid Waste Physical/Chemical Methods (SW-846)-to analyze milk for an expanded list of volatile organic compounds is presented. The milk matrix exhibits a strong affinity for organic compounds and the surrogate based matrix normalization described in method 8261 provided accurate results. This method had the sensitivity necessary to detect volatile organic analytes at or below maximum contaminant levels (MCLs) set by EPA for drinking water. In a survey of milk samples available in Las Vegas, Nevada, 32 of 88 targeted volatile organic compounds (VOCs) were detected. Many of the detected VOCs have not previously been reported and a rationale for their presence in milk is presented.

Animals↗