Literature DB >> 1487335

Human inhalation pharmacokinetics of chlorodifluoromethane (HCFC22).

B H Woollen1, J R Marsh, J D Mahler, T R Auton, D Makepeace, J Cocker, P G Blain.   

Abstract

Two groups of three male volunteers were exposed to atmospheric concentrations of either 327 or 1833 mg m-3 chlorodifluoromethane (HCFC22) for 4 h. Blood, urine and expired air samples were taken during and after the exposure period and analysed for HCFC22. Urine samples were also analysed for fluoride ion. During the exposure period, blood concentrations of HCFC22 approached a plateau, and the average peak blood concentrations of 0.25 and 1.36 micrograms cm-3 were proportional to dose. HCFC22 concentrations in expired air were similar to the exposure concentration during the exposure period. The ratio between venous blood and breath concentrations of HCFC22 towards the end of the exposure period was on average 0.77, which is consistent with in vitro estimates of the partition coefficient. In the post-exposure period, three phases for the elimination of HCFC22 were identified, with estimated half-lives of 0.005, 0.2 and 2.6h. HCFC22 was detected in urine samples taken in the post-exposure period, and the rate of decline was consistent with the terminal rate of elimination estimated from blood and breath measurements. On average 2.1% of the inhaled HCFC22 was recovered in breath within 26 h of exposure. This is consistent with the low solubility in blood and fat. Minimal changes in fluoride ion concentrations in urine following exposure indicate that HCFC22 is unlikely to be metabolised to a significant extent. Following inhalational exposure HCFC22 is poorly absorbed and is rapidly eliminated from the body. Possible biological monitoring strategies could be based on measurements of HCFC22 in urine or breath samples collected after the end of an exposure period.

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Year:  1992        PMID: 1487335     DOI: 10.1007/bf00379550

Source DB:  PubMed          Journal:  Int Arch Occup Environ Health        ISSN: 0340-0131            Impact factor:   3.015


  8 in total

1.  Human inhalation pharmacokinetics of 1,1,2-trichloro-1,2,2-trifluoroethane (FC113).

Authors:  B H Woollen; E A Guest; W Howe; J R Marsh; H K Wilson; T R Auton; P G Blain
Journal:  Int Arch Occup Environ Health       Date:  1990       Impact factor: 3.015

2.  Solubility of freon-22 in blood and lung tissue.

Authors:  P J Franks; R H Hooper; P R Jones
Journal:  Br J Anaesth       Date:  1989-04       Impact factor: 9.166

3.  Effect of alcohol on the kinetics of mandelic acid excretion in volunteers exposed to styrene vapour.

Authors:  H K Wilson; S M Robertson; H A Waldron; D Gompertz
Journal:  Br J Ind Med       Date:  1983-02

4.  A physiologically based mathematical model for the human inhalation pharmacokinetics of 1,1,2-trichloro-1,2,2-trifluoroethane.

Authors:  T R Auton; B H Woollen
Journal:  Int Arch Occup Environ Health       Date:  1991       Impact factor: 3.015

5.  Reference values of renal excretion of fluoride.

Authors:  W Massmann
Journal:  J Clin Chem Clin Biochem       Date:  1981-10

6.  Solubility of Freon 22 in human blood and lung tissue.

Authors:  N Varene; M L Choukroun; R Marthan; P Varene
Journal:  J Appl Physiol (1985)       Date:  1989-05

7.  Different pharmacokinetics of dichlorofluoromethane (CFC 21) and chlorodifluoromethane (CFC 22).

Authors:  H Peter; J G Filser; L von Szentpály; H J Wiegand
Journal:  Arch Toxicol       Date:  1986-04       Impact factor: 5.153

8.  Partition coefficients of some aromatic hydrocarbons and ketones in water, blood and oil.

Authors:  A Sato; T Nakajima
Journal:  Br J Ind Med       Date:  1979-08
  8 in total

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