Air to fat and blood to fat distribution of volatile organic compounds and drugs: linear free energy analyses

Partition coefficients, K(fat), from air to human fat and to rat fat have been collected for 129 volatile organic compounds, VOCs. A linear free energy relationship, LFER, correlates the 129 values of log K(fat) with R(2)=0.958 and a standard deviation, S.D., of 0.194 log units. Use of training and test sets gives a predictive assessment of around 0.20 log units. Combination of log K(fat) with our previously listed values of log K(blood) enables blood/plasma to fat partition coefficients, as log P(fat), to be obtained for 126 VOCs. These values can be correlated with R(2)=0.847, S.D.=0.304 log units; the latter is also our assessment of the predictive capability of the LFER. Values of log P(fat) have been collected for 46 drugs, and can be fitted to an LFER with R(2)=0.811 and S.D.=0.355 log units. Unlike partition into brain or muscle, the data for VOCs and drugs cannot be combined. There are marked discrepancies for PCBs for which partition from blood/plasma into fat is very much less than that calculated from the data on VOCs or from the data on drugs.     

Air to liver partition coefficients for volatile organic compounds and blood to liver partition coefficients for volatile organic compounds and drugs

Values of in vitro air to liver partition coefficients, K(liver), of VOCs have been collected from the literature. For 124 VOCs, application of the Abraham solvation equation to logK(liver) yielded a correlation equation with R(2)=0.927 and SD=0.26 log units. Combination of the logK(liver) values with logK(blood) values leads to in vitro blood to liver partition coefficients, as logP(liver) for VOCs; an Abraham solvation equation can correlate 125 such values with R(2)=0.583 and SD=0.23 log units. Values of in vivo logP(liver) for 85 drugs were collected, and were correlated with R(2)=0.522 and SD=0.42 log units. When the logP(liver) values for VOCs and drugs were combined, an Abraham solvation equation could correlate the 210 compounds with R(2)=0.544 and SD=0.32 log units. Division of the 210 compounds into a training set and a test set, each of 105 compounds, showed that the training equation could predict logP(liver) values with an average error of 0.05 and a standard deviation of 0.34 log units.     

Air to lung partition coefficients for volatile organic compounds and blood to lung partition coefficients for volatile organic compounds and drugs

Values of in vitro gas to lung partition coefficients, K(lung), of VOCs have been collected from the literature. For 44 VOCs, application of the Abraham solvation equation to log K(lung) yielded a correlation with R(2)=0.968 and S.D.=0.25 log units. Combination of the log K(lung) values with log K(blood) values leads to in vitro blood to lung partition coefficients, log P(lung) for 43 VOCs; an Abraham solvation equation correlated these values with a very poor R(2)=0.262 but with a very good S.D.=0.190 log units. Values of in vivo log P(lung) for 80 drugs were collected, and were correlated with R(2)=0.647 and S.D.=0.51 log units. When the log P(lung) values for VOCs and drugs were combined, an Abraham solvation equation could correlate the 123 compounds with R(2)=0.676 and S.D.=0.43 log units. Division of the 123 compounds into a training set and a test set, showed that the training equation could predict log P(lung) values with an average error of 0.001 and a standard deviation of 0.44 log units; for drugs in the combined test set the average error was 0.02 and the standard deviation 0.43 log units.     

低温等离子体对几种常见挥发性有机物的净化性能研究

目的 以低温等离子体净化器为依托,研究低温等离子体对甲苯、丙酮、乙酸乙酯和四氯化碳四种挥发性有机物的净化性能。
方法 通过单一组分挥发性有机物体系和双组分挥发性有机物体系进行净化率和净化动力学的研究。
结果 在单一组分挥发性有机物体系中,四种物质的净化率在300 min时均达到90%以上,各物质的净化动力学曲线符合指数方程C_t=C₀·e-kt,净化速率呈现出四氯化碳>甲苯>丙酮=乙酸乙酯的规律。在双组分挥发性有机物混合体系（丙酮、乙酸乙酯）中,相同条件下低温等离子体净化器对任一组分的净化率均低于单一组分,且各组分的净化存在竞争关系,相比于乙酸乙酯,净化器对丙酮的净化显示出更高的速率。
结论 低温等离子体对几种挥发性有机物的净化效果明显,净化速率快,该技术可为工作场所空气中挥发性有机物的高效净化提供依据。
     

Human exposure to volatile organic compounds: a comparison of organic vapor monitoring badge levels with blood levels

We undertook a study in Albany, New York, to investigate whether volatile organic compounds (VOCs) were measurable in the blood and in the breathing-zone air of people exposed to gasoline fumes and automotive exhaust. We sampled blood of 40 subjects, placed organic vapor badges on 40 subjects, and obtained personal breathing-zone samples from 24 subjects. We limited this analysis to 19 subjects who wore the organic vapor badges for at least 5 h. VOC levels, as determined by the organic vapor badges, were highly correlated with blood levels of these same compounds. Using detection in blood as the gold standard, we found the badges to be more sensitive than conventional charcoal tube samples in detecting low levels of methyl tert-butyl ether (0.60 vs 0.08), toluene (0.95 vs 0.64), and o-xylene (0.85 vs 0.64). In this study, organic vapor badges provided data on VOC exposure that correlated with blood assay results. These organic vapor badges might provide a convenient means of determining human exposure to VOCs in epidemiologic studies.     

Children's exposure to volatile organic compounds as determined by longitudinal measurements in blood

Blood concentrations of 11 volatile organic compounds (VOCs) were measured up to four times over 2 years in a probability sample of more than 150 children from two poor, minority neighborhoods in Minneapolis, Minnesota. Blood levels of benzene, carbon tetrachloride, trichloroethene, and m-/p-xylene were comparable with those measured in selected adults from the Third National Health and Nutrition Examination Survey (NHANES III), whereas concentrations of ethylbenzene, tetrachloroethylene, toluene, 1,1,1-trichloroethane, and o-xylene were two or more times lower in the children. Blood levels of styrene were more than twice as high, and for about 10% of the children 1,4-dichlorobenzene levels were greater than or equal to 10 times higher compared with NHANES III subjects. We observed strong statistical associations between numerous pairwise combinations of individual VOCs in blood (e.g., benzene and m-/p-xylene, m-/p-xylene and o-xylene, 1,1,1-trichloroethane and m-/p-xylene, and 1,1,1-trichloroethane and trichloroethene). Between-child variability was higher than within-child variability for 1,4-dichlorobenzene and tetrachloroethylene. Between- and within-child variability were approximately the same for ethylbenzene and 1,1,1-trichloroethane, and between-child was lower than within-child variability for the other seven compounds. Two-day, integrated personal air measurements explained almost 79% of the variance in blood levels for 1,4-dichlorobenzene and approximately 20% for tetrachloroethylene, toluene, m-/p-xylene, and o-xylene. Personal air measurements explained much less of the variance (between 0.5 and 8%) for trichloroethene, styrene, benzene, and ethylbenzene. We observed no significant statistical associations between total urinary cotinine (a biomarker for exposure to environmental tobacco smoke) and blood VOC concentrations. For siblings living in the same household, we found strong statistical associations between measured blood VOC concentrations.     

Variability of environmental exposures to volatile organic compounds

Although studies of occupational exposure to volatile organic compounds (VOCs) often partition variability across groups, and between and within persons, those of environmental exposure to VOCs have not involved such partitioning. Using data from the Environmental Protection Agency's total exposure assessment methodology (TEAM) studies, we partitioned exposure variability across cities, and between and within persons for nine VOCs. The estimated variance components decreased in the order: within-person > between-person > across city. Despite their smaller magnitudes, estimates of between-person and across-city variance components were sufficiently large to provide reasonable contrast for informative epidemiology studies of most VOCs. Estimates of between-person variance components for environmental VOCs were similar to those published for occupational VOCs (groups defined by job and factory). However, estimates of within-person variance components were much greater for environmental VOCs, probably due to the greater diversity of locations (including the workplace) visited by the general public over time. For benzene and perchloroethylene, we used a simple model to calculate numbers of personal measurements required to relate the exposure level to health outcome statistically. About 10 times more personal measurements would be required to investigate perchloroethylene exposure as compared to benzene exposure; this disparity reflects the greater within-subject variability of perchloroethylene data compared to benzene data. We conclude that variability should be partitioned for environmental VOC exposures in much the same manner as for occupational exposures. There should be sufficient variability in the levels of most VOCs across cities and between subjects to provide reasonable contrast for informative epidemiology studies, as we illustrate for exposures to benzene. Yet, epidemiologists should be wary of investigating environmental VOCs without preliminary data with which to estimate the variance structure of exposure variables.     

挥发性有机物对小鼠脑组织形态学和氨基酸类递质的影响

目的通过挥发性有机物(VOCs)对小鼠脑组织中递质类氨基酸含量的影响,探讨VOCs对小鼠神经系统的毒性。方法采用静式吸入染毒,小鼠亚急性暴露于挥发性有机物,设置对照、低(甲醛1.5mg/m3;VOCs20mg/m3)、中(甲醛4.5mg/m3;VOCs60mg/m3)、高浓度暴露组(甲醛13.5mg/m3;VOCs180mg/m3),染毒结束后,做脑组织常规病理,采用高效液相色谱法测定小鼠脑组织(皮质和海马)氨基酸类递质[包括兴奋性氨基酸类递质谷氨酸(Glu)、门冬氨酸(ASP);抑制性氨基酸类递质氨基丁酸(GABA)、甘氨酸(Gly)]含量。结果暴露组小鼠脑组织皮质和海马兴奋性氨基酸类递质含量随染毒浓度增加而降低,而抑制性氨基酸类递质含量随染毒浓度增加而增加。脑组织病理表现为VOCs暴露组神经元变性坏死。结论挥发性有机物引起小鼠学习记忆能力下降和麻醉作用。     

固相微萃取气相色谱法测定血中挥发性有机化合物

采用100μm 聚二甲基硅氧烷(PDMS)作为固相微萃取技术(SPME)装置的固相涂层,通过顶空固相微萃取气相色谱(HS-SPME-GC)法测定了血中10种挥发性有机化合物(VOCs)。实验确定的萃取时间为10分钟,解吸时间为1分钟。经研究证明,将萃取器针头完全插入气化室时解吸效果较佳,本法的重现性好(RSD< 5% ),线性范围较宽,其中四氯乙烯为25～10 000ng/m l,苯甲基环己烷10～1 000ng/m l,苯乙烯和异丙苯为1～1 000ng/m l,其他6种化合物为5～1 000ng/m l。血中10种VOCs的最低检出限均低于5ng/m l     

Relationships between levels of volatile organic compounds in air and blood from the general population

The relationships between levels of volatile organic compounds (VOCs) in blood and air have not been well characterized in the general population where exposure concentrations are generally at parts per billion levels. This study investigates relationships between the levels of nine VOCs, namely, benzene, chloroform, 1,4-dichlorobenzene, ethylbenzene, methyl tert-butyl ether (MTBE), tetrachloroethene, toluene, and m-/p- and o-xylene, in blood and air from a stratified random sample of the general US population. We used data collected from 354 participants, including 89 smokers and 265 nonsmokers, aged 20-59 years, who provided samples of blood and air in the National Health and Nutrition Examination Survey (NHANES) 1999-2000. Demographic and physiological characteristics were obtained from self-reported information; smoking status was determined from levels of serum cotinine. Multiple linear regression models were used to investigate the relationships between VOC levels in air and blood, while adjusting for effects of smoking and demographic factors. Although levels of VOCs in blood were positively correlated with the corresponding air levels, the strength of association (R(2)) varied from 0.02 (ethylbenzene) to 0.68 (1,4-DCB). Also the blood-air relationships of benzene, toluene, ethylbenzene, and the xylenes (BTEX) were influenced by smoking, exposure-smoking interactions, and by gender, age, and BMI, whereas those of the other VOCs were not. Interestingly, the particular exposure-smoking interaction for benzene was different from those for toluene, ethylbenzene, and the xylenes. Whereas smokers retained more benzene in their blood at increasing exposure levels, they retained less toluene, ethylbenzene, and xylenes at increasing exposure levels. Investigators should consider interaction effects of exposure levels and smoking when exploring the blood-air relationships of the BTEX compounds in the general population.     

Elimination of volatile organic compounds by biofiltration: a review

Volatile organic compounds (VOCs) are pollutants that are responsible for the formation of the tropospheric ozone, one of the precursors of smog. VOCs are emitted by various industries including chemical plants, pulp and paper mills, pharmaceuticals, cosmetics, electronics and agri-food industries. Some VOCs cause odor pollution while many of them are harmful to environment and human or animal health. For the removal of VOCs, biofiltration, a biological process, has proved to be reliable when properly operated. This process has therefore been widely applied in Europe and North America. The main advantages associated with the use of biofiltration are related to its set-up, maintenance, and operating costs which are usually lower than those related to other VOCs control technologies and because it is less harmful for the environment than conventional processes like incineration. In the present paper, the main parameters (type, moisture, pH, and temperature of filter bed, microbial population, nutrients concentrations, and VOCs' inlet load) to be controlled during the biofiltration are identified and described in detail. The main phenomena involved in biofiltration are also discussed. For improving the efficiency of VOC control biotechnology, new techniques are now proposed that include the use of membranes, biphasic reactors, UV photolysis, and many others.     

室内挥发性有机物的来源及其健康效应

挥发性有机物 (VOCs)作为一大类空气污染物 ,是近几年来室内空气污染的热点问题 ,现代人一天之中有 90 %的时间在室内度过 ,所以VOCs对人体健康有着极大的危害 ,本文主要综述了VOCs的来源、种类及其对人体健康的影响。     

The influence of personal activities on exposure to volatile organic compounds

Seven persons volunteered to perform 25 common activities thought to increase personal exposure to volatile organic chemicals (VOCs) during a 3-day monitoring period. Personal, indoor, and outdoor air samples were collected on Tenax cartridges three times per day (evening, overnight, and daytime) and analyzed by GC-MS for 17 target VOCs. Samples of exhaled breath were also collected before and after each monitoring period. About 20 activities resulted in increasing exposure to one or more of the target VOCs, often by factors of 10, sometimes by factors of 100, compared to exposures during the sleep period. These concentrations were far above the highest observed outdoor concentrations during the length of the study. Breath levels were often significantly correlated with previous personal exposures. Major exposures were associated with use of deodorizers (p-dichlorobenzene); washing clothes and dishes (chloroform); visiting a dry cleaners (1,1,1-trichloroethane, tetrachloroethylene); smoking (benzene, styrene); cleaning a car engine (xylenes, ethylbenzene, tetrachloroethylene); painting and using paint remover (n-decane, n-undecane); and working in a scientific laboratory (many VOCs). Continuously elevated indoor air levels of p-dichlorobenzene, trichloroethylene, 1,1,1-trichloroethane, carbon tetrachloride, decane, and undecane were noted in several homes and attributed to unknown indoor sources. Measurements of exhaled breath suggested biological residence times in tissue of 12-18 hr and 20-30 hr for 1,1,1-trichloroethane and p-dichlorobenzene, respectively.     

Determinants of exposure to volatile organic compounds in four Oklahoma cities

To begin to develop generalized models for estimating personal exposure to ambient air pollutants within diverse populations, the design of the Oklahoma Urban Air Toxics Study incorporated eight dichotomous macroenvironmental and household factors that were hypothesized to be potential determinants of exposure. Personal, indoor, and outdoor samples of volatile organic compounds (VOCs) were collected over 24-h monitoring periods in 42 households, together with activity diaries and data on the participants' residences. The distributions of the VOC concentrations were moderately to highly left-censored, and were mostly bimodal. The ATSDR minimal risk level (MRL) was exceeded in a small number of the samples. Personal and indoor concentrations tended to be higher than outdoor concentrations, indicating that indoor exposures were dominated by indoor sources. However, indoor concentrations were not correlated with the permeability of the residence, suggesting that the observed indoor concentrations reflected mostly localized, short-term emissions. The influence of the eight dichotomous factors and of the presence of an attached garage was evaluated using the Wilcoxon rank-sum test and by comparison of "excursion fractions", that is, the fractions of each distributions exceeding 10% of the MRL. Dry weather and absence of children in the household were found to be associated with higher exposures in personal or indoor exposures. Given the small sample size, it is possible that these factors were confounded with unidentified household characteristics or activities that were the true determinants of exposure.     

Levels of volatile organic compounds in homes in Dalian,China

This paper measured selected individual volatile organic compounds (VOCs), including formaldehyde, in residences in Dalian, evaluated the association between the apartment characteristics and VOC concentrations, and explored the associations between chemicals and sick building syndrome (SBS). Higher VOC concentrations were measured indoors than outdoors in summer (August to September) and winter (January to March) in Dalian, and there were no strong correlations between the indoor and outdoor concentrations of most VOCs. This indicates the dominance of indoor sources as compared to outdoor sources. Formaldehyde was the most abundant compound in this study, followed by toluene, benzene, xylene, and styrene. These pollutants increase the occurrence of SBS. Thus, the VOC levels in dwellings in Dalian should be regulated, in view of SBS risks.     

Exposure to wood dust, resin acids, and volatile organic compounds during production of wood pellets

The main aim of this study was to investigate exposure to airborne substances that are potentially harmful to health during the production of wood pellets, including wood dust, monoterpenes, and resin acids, and as an indicator of diesel exhaust nitrogen dioxide. In addition, area measurements were taken to assess background exposure levels of these substances, volatile organic compounds (VOCs), and carbon monoxide. Measurements were taken at four wood pellet production plants from May 2004 to April 2005. Forty-four workers participated in the study, and a total of 68 personal measurements were taken to determine personal exposure to wood dust (inhalable and total dust), resin acids, monoterpenes, and nitrogen dioxide. In addition, 42 measurements of nitrogen dioxide and 71 measurements of total dust, resin acids, monoterpenes, VOCs, and carbon monoxide were taken to quantify their indoor area concentrations. Personal exposure levels to wood dust were high, and a third of the measured levels of inhalable dust exceeded the Swedish occupational exposure limit (OEL) of 2 mg/m3. Parallel measurements of inhalable and total dust indicated that the former were, on average, 3.2 times higher than the latter. The data indicate that workers at the plants are exposed to significant amounts of the resin acid 7-oxodehydroabietic acid in the air, an observation that has not been recorded previously at wood processing and handling plants. The study also found evidence of exposure to dehydroabietic acid, and exposure levels for resin acids approached 74% of the British OEL for colophony, set at 50 microg/m3. Personal exposure levels to monoterpenes and nitrogen dioxide were low. Area sampling measurements indicated that aldehydes and terpenes were the most abundant VOCs, suggesting that measuring personal exposure to aldehydes might be of interest. Carbon monoxide levels were under the detection limit in all area measurements. High wood dust exposure levels are likely to have implications for worker health; therefore, it is important to reduce exposure to wood dust in this industry.     

Public bus and taxicab drivers' work-time exposure to aromatic volatile organic compounds

Information on the work-time exposure of public bus and taxicab drivers to volatile organic compounds (VOCs) may be a critical factor in exploring the association between occupational exposure and health effects. Accordingly, this study evaluated the work-time VOC exposure of public bus and taxicab drivers by measurement of six selected aromatic VOC concentrations in the personal air of public bus and taxicab drivers during winter and summer. Two groups of five public bus drivers (smokers and nonsmokers) and two groups of five taxicab drivers (smokers and nonsmokers) were recruited for the study. The taxicab drivers were found to be exposed to higher aromatic compound levels than the bus drivers during their daily work time. The personal exposure of the bus and taxicab drivers was influenced by whether or not they smoked plus the season. It was also established that the potential exposure of bus drivers to aromatic VOCs did not exceed that of an unemployed reference group, whereas the potential exposure of taxicab drivers did. Meanwhile, based on comparison of the calculated in-vehicle concentrations with those from a previous study, the VOC levels inside public buses and taxicabs were found to be lower than those inside automobiles.     

Ozone and volatile organic compounds in the metropolitan area of Lima-Callao,Peru

This study analyzes ozone formation in the metropolitan area of Lima-Callao as a function of meteorological patterns and the concentrations of nitrogen oxides and reactive organic gases. The study area is located on the west coast of South America (12°S) in an upwelling region that is markedly affected by the Southeast Pacific anticyclone. The vertical stability and diurnal evolution of the mixing layer were analyzed from radiosondes launched daily during 1992–2014 and from two intensive campaigns in 2009. Vertical profiles show that during June–November, the subsidence inversion base ranges from 0.6 to 0.9 km above sea level (asl). In contrast, during December–May, subsidence inversion dissipates, leading to weak surface inversions from 0.1 to 0.6 km asl. At the surface level, compliance with the ozone standard of 51 parts per billion by volume (ppbv) is explained by the marine boundary layer effect and by strong inhibition of ozone formation due to titration with nitric oxide. Day-of-the-week variations in ozone and nitrogen oxides suggest a VOC-limited ozone-formation regime in the atmosphere of Lima. Furthermore, the pattern of C₆–C₁₂ species indicates that gasoline-powered vehicles are the main source of volatile organic compounds (VOCs), whereas the species with the greatest ozone-forming potential corresponded to the sum of the isomers m- and p-xylene. Mean benzene concentrations exceeded the standard of 0.63 ppbv, reaching 1.2 ppbv east of Lima. Nevertheless, the cancer risk associated with the inhalation of benzene was deemed acceptable, according to USEPA and WHO criteria.     

Risk assessment of exposure to volatile organic compounds in different indoor environments

The lifetime cancer risks of exposure of cooks and food service workers, office workers, housewives, and schoolchildren in Hong Kong to volatile organic compounds (VOCs) in their respective indoor premises during normal indoor activities were assessed. The estimated cancer risk for housewives was the highest, and the second-highest lifetime cancer risk to VOC exposure was for the groups of food service and office workers. Within a certain group of the population, the lifetime cancer risk of the home living room was one to two orders of magnitude higher than that in other indoor environments. The estimated lifetime risks of food service workers were about two times that of office workers. Furthermore, the cancer risks of working in kitchen environments were approximately two times higher than the risks arising from studying in air-conditioned classrooms. The bus riders had higher average lifetime cancer risks than those travelling by Mass Transit Railway. For all target groups of people, the findings of this study show that the exposures to VOCs may lead to lifetime risks higher than 1 x 10(-6). Seven indoor environments were selected for the measurement of human exposure and the estimation of the corresponding lifetime cancer risks. The lifetime risks with 8-h average daily exposures to individual VOCs in individual environments were compared. People in a smoking home had the highest cancer risk, while students in an air-conditioned classroom had the lowest risk of cancer. Benzene accounted for about or more than 40% of the lifetime cancer risks for each category of indoor environment. Nonsmoking and smoking residences in Hong Kong had cancer risks associated with 8-h exposures of benzene above 1.8 x 10(-5) and 8.0 x 10(-5), respectively. The cancer risks associated with 1,1-dichloroethene, chloroform, methylene chloride, trichloroethene, and tetrachloroethene became more significant at selected homes and restaurants. Higher lifetime cancer risks due to exposure to styrene were only observed in the administrative and printing offices and air-conditioned classrooms. Higher lifetime cancer risks related to chloroform exposures were observed at the restaurant and the canteen.