Effect of acrylate chemistry on human health.

OBJECTIVES: The prospective cohort study of 1992-1999 describes the effect of occupational exposure to chemical substances in the production of acrylic acid, acrylic acid esters and acrylate dispersions at the various workplaces of one chemical plant. METHODS: Exposure to selected chemicals (acrylonitrile, n-butanol, butyl acrylate, ethyl acrylate, methyl acrylate, methyl methacrylate, toluene, and styrene) was determined by personal passive dosimetry (GC/MS method). The annual examinations included general health, by guided interview, a general medical examination, hematological and biochemical examinations, examination of the parameters of serum immunity and selected tumor markers, and spirometry. The authors also repeatedly performed cytogenetic analysis of human peripheral lymphocytes. RESULTS: The authors followed a group of 120 employees (60 exposed, 60 controls), mean age 40+/-8 years in both groups, with average period of exposure to chemicals (exposed group) 13+/-5 years. The measured concentrations of chemicals in the working atmosphere were generally low; maximum allowable concentrations (MAC) values or suggested limits of certain chemicals were occasionally exceeded (most frequently for butyl acrylate). The results of the examination of the workers over the 8 years have not revealed any marked differences between the exposed and control groups that could be attributable solely to the acrylate exposure. CONCLUSIONS: Exposure to chemical substances at the workplace was relatively low, the limits being exceeded only sporadically (each such case was investigated at the workplace), and the level of exposure continues to decrease gradually over the years. Considering the fact that the exposed individuals are expected to work for 23 additional years on average, we feel that long-term monitoring of selected health-related parameters, not including tumor markers, appears desirable. The examination of tumor markers has not contributed to the problem evaluation for a number of false-positive results.

A rapid and simple method for the analysis of 1-hydroxypyrene glucuronide: a potential biomarker for polycyclic aromatic hydrocarbon exposure.

The present study describes a simple method of analyzing metabolites of pyrene in urine. This method is capable of detecting the glucuronic acid and sulfate conjugates of pyrene as well as free 1-hydroxypyrene in a single analysis. In comparison to other analytical methods for detecting pyrene metabolites, this new method does not require an overnight enzymatic hydrolysis step and is much more rapid method of analysis. The newly developed procedure involves solid phase extraction of pyrene metabolites followed by separation using HPLC with a phenyl modified reverse phase column and an acidic buffer and acetonitrile gradient elution system. Metabolites were detected using a fluorescence detector with wavelength conditions optimized for each metabolite. This method resulted in baseline separation of the glucuronic acid (1-OH P-GlcUA) and sulfate conjugate (1-OH P-Sul) of 1-hydroxypyrene and free 1-hydroxypyrene (1-OH P). The potential of this method for use in monitoring human exposure to mixtures of PAHs was evaluated by analyzing urine obtained from five individuals working in a coal gasification plant. 1-OH P-GlcUA was detected as the major metabolite in the urine of all the five workers. This metabolite accounted for 80-100% of the total pyrene metabolites excreted in urine. 1-OH P-GlcUA levels ranged from 0.31-0.94 microgram/g creatinine. Low levels of the sulfate conjugate (0.002-0.06 microgram/g creatinine) were detected in four of the samples while free 1-hydroxypyrene (0.07-0.2 microgram/g creatinine) was detected in two of the five urine samples. Urine from occupationally exposed workers was also analyzed for 1-hydroxypyrene following enzymatic hydrolysis using the standard approach. Levels of 1-hydroxypyrene ranged from 0.51-1.17 micrograms/g creatinine. Comparison of the fluorescence intensities of 1-OH P-GlcUA and 1-OH P-Sul to 1-hydroxypyrene demonstrated that the glucuronide conjugate is 3-fold more fluorescent and the sulfate conjugate is 4-fold more fluorescent than 1-hydroxypyrene. These results indicate that conjugates of pyrene, specifically, 1-OH P-GlcUA can potentially be used as a more sensitive biomarker of exposure to PAHs.