Literature DB >> 6396052

Effects of biosolubility on pulmonary uptake and disposition of gases and vapors of lipophilic chemicals.

V Fiserova-Bergerova, M Tichy, F J Di Carlo.   

Abstract

Since statistical analysis proved the intercorrelation of tissue-gas partition coefficients of chemicals with similar chemical structures, bioavailability is controlled by one parameter dependent on the physicochemical properties of the chemicals and two constants distinguishing the tissues. Oil-gas partition coefficients are suggested to describe the biosolubility of volatile halogenated aliphatic chemicals. Tissue-gas partition coefficients derived from oil-gas partition coefficients were substituted in a pharmacokinetic model in order to study the effect of biosolubility on uptake, distribution, and elimination of inhaled chemicals. The simulation was focused on occupational exposures (8 h/day, 5 days/wk). Desaturation curves for all tissues show three exponential decays. The analysis of the simulation data indicates three patterns in behavior of inhaled vapors and gases in the body. Tissue uptake of poorly soluble chemicals (oil-gas partition coefficient less than 10) is flow limited at the beginning of exposure, but the partial pressures of such chemicals in the body equilibrate very rapidly with ambient air. Increased pulmonary uptake compensates for metabolic clearance. The rapid response of tissue concentrations to changes in exposure concentrations indicates that the toxic effect can easily be induced by short-term increase of exposure concentration, and that emergence from the reversible effect is rapid when exposure ceases. Tissue uptake of chemicals with oil-gas partition coefficients between 10 and 10(4) is flow limited during the entire 8-h exposure. Tissue concentrations increase slowly. Pulmonary uptake, being restricted by alveolar ventilation, compensates at steady state only for the amount of chemical removed by metabolic clearance. Therefore, tissue concentrations at steady state are lower than biosolubility. Accumulation during occupational exposure is obvious. Dumping of inhaled chemicals in adipose tissue protects the target organ from the occasional short-term increases in the exposure concentration. Tissue uptake of highly soluble chemicals (oil-gas partition coefficients greater than 10(4)) is limited by alveolar ventilation and exposure concentration. The rising and declining of tissue concentrations is very slow, half-times being in the magnitude of months and years. Metabolism reduces the half-time significantly. A lagging acute toxic effect can develop as the chemical accumulates in the body; the effect is most likely to persist long after the termination of the exposure.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1984        PMID: 6396052     DOI: 10.3109/03602538409033557

Source DB:  PubMed          Journal:  Drug Metab Rev        ISSN: 0360-2532            Impact factor:   4.518


  12 in total

1.  Prediction of in vivo tissue distribution from in vitro data. 3. Correlation between in vitro and in vivo tissue distribution of a homologous series of nine 5-n-alkyl-5-ethyl barbituric acids.

Authors:  Peter Ballard; David E Leahy; Malcolm Rowland
Journal:  Pharm Res       Date:  2003-06       Impact factor: 4.200

2.  Prediction of in vivo tissue distribution from in vitro data. 2. Influence of albumin diffusion from tissue pieces during an in vitro incubation on estimated tissue-to-unbound plasma partition coefficients (Kpu).

Authors:  Peter Ballard; Philip A Arundel; David E Leahy; Malcolm Rowland
Journal:  Pharm Res       Date:  2003-06       Impact factor: 4.200

3.  Use of linear free energy relationships in toxicology: prediction of partition coefficients of volatile lipophilic compounds.

Authors:  G A Csanády; R J Laib
Journal:  Arch Toxicol       Date:  1990       Impact factor: 5.153

Review 4.  Modeling kinetics of subcellular disposition of chemicals.

Authors:  Stefan Balaz
Journal:  Chem Rev       Date:  2009-05       Impact factor: 60.622

5.  Determination and prediction of tissue-gas partition coefficients.

Authors:  V Fiserova-Bergerova; M L Diaz
Journal:  Int Arch Occup Environ Health       Date:  1986       Impact factor: 3.015

6.  A Physiologically Based Pharmacokinetic Model for Naphthalene With Inhalation and Skin Routes of Exposure.

Authors:  Dustin F Kapraun; Paul M Schlosser; Leena A Nylander-French; David Kim; Erin E Yost; Ingrid L Druwe
Journal:  Toxicol Sci       Date:  2020-10-01       Impact factor: 4.849

7.  Effect of various exposure scenarios on the biological monitoring of organic solvents in alveolar air. I. Toluene and m-xylene.

Authors:  S Laparé; R Tardif; J Brodeur
Journal:  Int Arch Occup Environ Health       Date:  1993       Impact factor: 3.015

8.  Human physiologic factors in respiratory uptake of 1,3-butadiene.

Authors:  Y S Lin; T J Smith; K T Kelsey; D Wypij
Journal:  Environ Health Perspect       Date:  2001-09       Impact factor: 9.031

9.  Association of the blood/air partition coefficient of 1,3-butadiene with blood lipids and albumin.

Authors:  Yu-Sheng Lin; Thomas J Smith; David Wypij; Karl T Kelsey; Frank M Sacks
Journal:  Environ Health Perspect       Date:  2002-02       Impact factor: 9.031

10.  PBTK modeling demonstrates contribution of dermal and inhalation exposure components to end-exhaled breath concentrations of naphthalene.

Authors:  David Kim; Melvin E Andersen; Yi-Chun E Chao; Peter P Egeghy; Stephen M Rappaport; Leena A Nylander-French
Journal:  Environ Health Perspect       Date:  2007-02-14       Impact factor: 9.031

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