Adjusting exposure limits for long and short exposure periods using a physiological pharmacokinetic model
Andersen, ME; Macnaughton, MG; Clewell HJ III; Paustenbach, DJ
HERO ID
4233
Reference Type
Journal Article
Year
1987
Language
English
PMID
| HERO ID | 4233 |
|---|---|
| In Press | No |
| Year | 1987 |
| Title | Adjusting exposure limits for long and short exposure periods using a physiological pharmacokinetic model |
| Authors | Andersen, ME; Macnaughton, MG; Clewell HJ III; Paustenbach, DJ |
| Journal | AIHA Journal |
| Volume | 48 |
| Issue | 4 |
| Page Numbers | 335-343 |
| Abstract | The rationale for adjusting occupational exposure limits for unusual work schedules is to assure, as much as possible, that persons on these schedules are placed at no greater risk of injury or discomfort than persons who work a standard 8 hr/day, 40 hr/week. For most systemic toxicants, the risk index upon which the adjustments are made will be either peak blood concentration or integrated tissue dose, depending on what chemical's presumed mechanism of toxicity. Over the past ten years, at least four different models have been proposed for adjusting exposure limits for unusually short and long work schedules. This paper advocates use of a physiologically-based pharmacokinetic (PB-PK) model for determining adjustment factors for unusual exposure schedules, an approach that should be more accurate than those proposed previously. The PB-PK model requires data on the blood:air and tissue:blood partition coefficients, the rate of metabolism of the chemical, organ volumes, organ blood flows and ventilation rates in humans. Laboratory data on two industrially important chemicals--styrene and methylene chloride--were used to illustrate the PB-PK approach. At inhaled concentrations near their respective 8-hr Threshold Limit Value-Time-weighted averages (TLV-TWAs), both of these chemicals are primarily eliminated from the body by metabolism. For these two chemicals, the appropriate risk indexing parameters are integrated tissue dose or total amount of parent chemical metabolized. Since methylene chloride is metabolized to carbon monoxide, the maximum blood carboxyhemoglobin concentrations also might be useful as an index of risk for this chemical.(ABSTRACT TRUNCATED AT 250 WORDS) |
| Doi | 10.1202/0002-8894(1987)048<0335:AELFLA>2.0.CO;2 |
| Pmid | 3591649 |
| Wosid | WOS:A1987G854800007 |
| Url | https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023259832&doi=10.1080%2f15298668791384850&partnerID=40&md5=4dc9b356ec4624b6fc935bec63d9967b |
| Is Certified Translation | No |
| Dupe Override | No |
| Comments | 1987b in 204,00.Am. Ind. Hyg. Assoc. J. 48: 335-343. |
| Is Public | Yes |
| Language Text | English |
| Keyword | Absorption; Distribution; Metabolism; Excretion; Protein binding; Pharmacokinetic/pharmacodynamic modeling; QSAR; QSPR; Molecular modeling |
| Is Qa | No |