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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    International archives of occupational and environmental health 63 (1991), S. 77-79 
    ISSN: 1432-1246
    Keywords: Epoxy resin ; Hexahydrophthalic anhydride ; Hexahydrophthalic acid ; Urinary excretion ; Biological monitoring
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Post-shift and next-morning urine was sampled from workers exposed to hexahydrophtalic anhydride (HHPA), an epoxy hardener, sensitising at low exposure levels. Exposure levels of HHPA in air gas chromatography, GC) in the range of 30–270 μg/m3 corresponded to urinary concentrations of 0.9–2.8 μmol hexahydrophthalic acid (HHP acid; GC-mass spectrometry)/mmol creatinine. In the morning samples the concentrations were 〈0.04-0.3 μmol HHP acid/mmol creatinine. In unexposed controls, the level was 〈0.1 μmol/mmol creatinine. A correlation was found between the time-weighted levels of HHPA in air and HHP acid in the post-shift urine (r s = 0.93; P 〈 0.023), indicating that the determination of HHP acid in urine is suitable for biologic monitoring of HHPA exposure.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    International archives of occupational and environmental health 73 (2000), S. 228-234 
    ISSN: 1432-1246
    Keywords: Key words Acid anhydrides ; Occupational asthma ; Exposure assessment ; Allergy ; Biological monitoring ; Specific IgE ; Specific IgG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Objectives: To clarify whether the intensity of exposure to organic acid anhydrides (OAAs) is associated with the risk of sensitisation to these allergens. Methods: The investigations were carried out in three different manufacturing plants (A, B, and C) where OAAs were used in the production of epoxy resins. Methyltetrahydrophthalic acid anhydride (MTHPA) was used in all three plants. The exposure assessment included stationary and ambient air monitoring (OAAs in the air) and biological monitoring (metabolites in urine). In plant A 20, in plant B 86 and in plant C 113 employees were examined by a physician (anamnesis, skin-prick test, specific IgE, spirometry). In plants B and C, the exposure areas were classified as high, medium, and low, without the results of the exposure assessment being known. Results: The ambient air concentrations (in μg/m3) of MTHPA were 37.2 and 58.5 in plant A (number of samples n=2), ranged from 〈0.5–26.2 in plant B (n=5) and from 2.1–57.9 in plant C (n=3) with stationary air collecting, and from 8–45 (n=6), from 〈4.7–35.7 (n=3) and from 2–37.8 (n=3) with personal air collection. The metabolites of OAAs in urine (in nmol/mmol creatinine) ranged from 5.7–645 (median of MTHPA: 346) in plant A, from 〈1–213 (median of MTHPA: 10.1) in plant B and from 0.1–830 (median of the sum of the OOA metabolites: 108.6) in plant C. The prevalence of sensitisation was 35% in plant A, 21% in plant B and 29% in plant C. A higher prevalence in the highly exposed areas, however, could not be seen. Levels of IgE specific for conjugates of MTHPA were not associated with the metabolites in the end of shift urine. Levels of IgG specific for conjugates of MTHPA, however, were associated with the metabolites in the end of shift urine. Conclusions: The data showed that biological monitoring is a useful tool in the exposure assessment of OAAs. Comparing the prevalence of sensitisation and the results of biological monitoring, between the three plants, we found that sensitisation increased with increasing exposure. Within a plant a higher risk of sensitisation in persons working in highly exposed areas at the time of the examination could not be seen, possibly due to frequent job rotation.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    International archives of occupational and environmental health 65 (1993), S. 43-47 
    ISSN: 1432-1246
    Keywords: Hexahydrophthalic anhydride ; Hexahydrophthalic acid ; Urine ; Skin absorption ; Biological monitoring
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Urinary hexahydrophthalic acid (HHP acid) levels were determined in 20 workers occupationally exposed to hexahydrophthalic anhydride (HHPA) air levels of 11–220μg/m3. The levels of HHP acid in urine increased rapidly during exposure and the decreases were also rapid after the end of exposure. The elimination half-time of HHP acid was 5h, which was significantly longer than in experimentally exposed volunteers, possibly indicating distribution to more than one compartment. There was a close correlation between time-weighted average levels of HHPA in air and creatinine-adjusted levels of HHP acid in urine collected during the last 4 h of exposure (r = 0.90), indicating that determination of urinary HHP acid levels is suitable as a method for biological monitoring of HHPA exposure. An air level of 100 μg/m3 corresponded to a postshift urinary HHP acid level of ca. 900 nmol/mmol creatinine in subjects performing light work for 8h. Percutaneous absorption of HHPA was studied by application of HHPA in petrolatum to the back skin of three volunteers. The excreted amounts of HHP acid in urine, as a fraction of the totally applied amount of HHPA, were within intervals of 1.4%–4.5%, 0.2%–1.3%, and 0%–0.4% respectively, indicating that the contribution from percutaneous absorption is of minor importance in a method for biological monitoring.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1612-1112
    Keywords: Gas chromatography-mass spectrometry ; Hexahydrophthalic and methylhexahydrophthalic acid ; Pentafluorobenzyl derivatives ; Biological monitoring ; Industrial hygiene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A method for determining hexahydrophthalic (HHP acid) and methylhexahydrophthalic acids (MHHP acid) from human urine was developed. These acids are metabolites of the highly sensitising hexahydrophthalic anhydride and methylhexahydrophthalic anhydride. The acids were purified from urine by liquid-solid extraction and derivatised with pentafluorobenzyl bromide to the corresponding esters. These were analysed by GC-MS in the negative-ion chemical-ionisation mode with ammonia moderating gas. Deuterium labelled HHP acid and MHHP acid were internal standards. The precision for HHP acid was 3–6% in the range 70–620 ng mL−1 and that for MHHP acid was 2–8% in the range 60–680 ng mL−1. Overall recovery of HHP acid from urine was 74–88% and that for MHHP acid 98–101%. Detection limits were 11 ng HHP acid mL−1 urine and 17 ng MHHP acid mL−1 urine. There were no significant differences between determinations of HHP acid by a previous method and the present method. Some instability of the acids in urine were found after extended storage at −20°C. The method was applicable for determination of HHP acid and MHHP acid from exposed workers.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 43 (1996), S. 668-670 
    ISSN: 1612-1112
    Keywords: Gas chromatography-mass spectrometry ; Methylhexahydrophthalic acid ; Biological monitoring ; Industrial hygiene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A method for analysis of urinary methylhexahydrophthalic acid (MHHP acid), a metabolite of the highly sensitising methylhexahydrophthalic anhydride, is described. The method is based on a double liquid-solid extraction of the MHHP acid from urine, esterification with methanol and boron trifluoride catalysis, and analysis with gas chromatography-mass spectrometry in the electron impact mode. The detection limit was 3 ng mL−1 and the precision between 2 and 5% in the range 34 to 340 ng mL−1. The method gave similar results compared to another method. Urine stored for five years at −20°C lost between 38 and 86% of the MHHP acid (range 16–85 ng mL−1).
    Type of Medium: Electronic Resource
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