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Annals of Occupational Hygiene Advance Access published online on May 26, 2006

Annals of Occupational Hygiene, doi:10.1093/annhyg/mel024
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© The Author 2006. Published by Oxford University Press on behalf of the British Occupational Hygiene Society
Received November 9, 2005
Accepted February 21, 2006

Article

Assessing Isocyanate Exposures in Polyurethane Industry Sectors Using Biological and Air Monitoring Methods

K. S. Creely 1 *, G. W. Hughson 1, J. Cocker 2, and K. Jones 2

1 Institute of Occupational Medicine, Research Avenue North, Riccarton, Edinburgh, UK
2 Health and Safety Laboratory, Harpur Hill, Buxton, UK

* To whom correspondence should be addressed.
K. S. Creely, E-mail: karen.creely{at}iom-world.org


   Abstract

Isocyanates, as a chemical group, are considered to be the biggest cause of occupational asthma in the UK. Monitoring of airborne exposures to total isocyanate is costly, requiring considerable expertise, both in terms of sample collection and chemical analysis and cannot be used to assess the effectiveness of protection from wearing respiratory protective equipment (RPE). Biological monitoring by analysis of metabolites in urine can be a relatively simple and inexpensive way to assess exposure to isocyanates. It may also be a useful way to evaluate the effectiveness of control measures in place. In this study biological and inhalation monitoring were undertaken to assess exposure in a variety of workplaces in the non-motor vehicle repair sector. Companies selected to participate in the survey included only those judged to be using good working practices when using isocyanate formulations. This included companies that used isocyanates to produce moulded polyurethane products, insulation material and those involved in industrial painting. Air samples were collected by personal monitoring and were analysed for total isocyanate content. Urine samples were collected soon after exposure and analysed for the metabolites of different isocyanate species, allowing calculation of the total metabolite concentration. Details of the control measures used and observed contamination of exposed skin were also recorded. A total of 21 companies agreed to participate in the study, with exposure measurements being collected from 22 sites. The airborne isocyanate concentrations were generally very low (range 0.0005-0.066 mg m-3). A total of 50 of the 70 samples were <0.001 mg m-3, the limit of quantification (LOQ), therefore samples below the LOQ were assigned a value of 1/2 LOQ (0.0005 mg m-3). Of the 70 samples, 67 were below the current workplace exposure limit of 0.02 mg m-3. The highest inhalation exposures occurred during spray painting activities in a truck manufacturing company (0.066 mg m-3) and also during spray application of polyurethane foam insulation (0.023 mg m-3). The most commonly detected isocyanate in the urine was hexamethylene diisocyanate, which was detected in 21 instances. The geometric mean total isocyanate metabolite concentration for the dataset was 0.29 µmol mol-1 creatinine (range 0.05-12.64 µmol mol-1 creatinine). A total of 23 samples collected were above the agreed biological monitoring guidance value of 1.0 µmol mol-1 creatinine. Activities that resulted in the highest biological monitoring results of the dataset included mixing and casting of polyurethane products (12.64 µmol mol-1 creatinine), semi-automatic moulding (4.80 µmol mol-1 creatinine) and resin application (3.91 µmol mol-1 creatinine). The biological monitoring results show that despite low airborne isocyanate concentrations, it was possible to demonstrate biological uptake. This tends to suggest high sensitivity of the biological monitoring method and/or that in some instances the RPE being used by operators was not effective or that absorption may have occurred via dermal or other routes of exposure. This study demonstrates that biological monitoring is a useful tool when assessing worker exposure to isocyanates, providing a more complete picture on the efficacy of control measures in place than is possible by air monitoring alone. The results also demonstrated that where control measures were judged to be adequate, most biological samples were close to or <1 µmol mol-1 creatinine, the agreed biological monitoring benchmark.


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