January 2005 LABORATORY Health Guidance Values (HGVs) are set at a level at which there is no indication from the scientific evidence available that the Method for Polycyclic Aromatic Hydrocarbons substance being monitored is likely to be injurious to health. Values not greatly in excess of a HGV are unlikely to produce serious short Hazardous Substance: or long term effects on health. However, Polycyclic Aromatic Hydrocarbons regularly exceeding the HGV does indicate that control of exposure may not be adequate Maximum exposure limit withdrawn controlled. Under these circumstances employers will need to look at current work practices to see how they can be improved to reduce exposure.
Biological Monitoring Guidance Value:
Benchmark value - 4 mol 1-hydroxypyrene /mol creatintine in urine For further advice contact: Conversion: 1 mol/mol = 1.93 g/g
Group Support Unit
Room L.2.51 Health and Safety Laboratory Harpur Hill Buxton SK17 9JN
Telephone: 01298 218099 Fax: 01298 218172
Website: www.hsl.gov.uk The Health and Safety Laboratory is an Agency of the Health and Safety Executive Sample Collection Other Information
Time: Urine samples collected at the end of shift Elimination half-time
Equipment: Polystyrene universal container (30ml) 1-hydroxypyrene in urine has half lives of about 5.5 hours, 23h and over 300h. Description of Suggested Method Confounding Factors Urine (200l) is incubated at 37OC for 4h with glucurase before None known although use of coal tar products (such as injection onto a C18 HPLC column. Detection is by fluorescence shampoos) can increase 1-hydroxypyrene levels significantly with an excitation wavelength of 242 nm and an emission and any use should be noted. wavelength of 398 nm. Unexposed Levels Sample Transport to Laboratory < 2 mol hydroxypyrene/mol creatine
At ambient temperature, samples should arrive within 48h of Creatinine Correction
collection. If delay anticipated store for up to 7 days in Advised refrigerator, longer term storage at -20OC. Samples sent through postal system must comply with Post Office regulations. Quality Assurance
Analytical Evaluation Internal QC - must be established
External QA - G-EQUAS (www.g-equas.de) Precision - within day <8% RSD at 40 nmol/l - day to day <7% RSD at 250 nmol/l Detection Limit - 3x background - 5 nmol/l Calibration Range - typically 5-100 nmol/l Sample Stability - 2 days at ambient, >3 months at -20oC Analytical Interferences - None known