Disposition of propargyl alcohol in rat and mouse after intravenous, oral, dermal and inhalation exposure

• Published in: Xenobiotica Vol. 31; no. 6; pp. 357 - 375
• Main Authors: Dix, K. J., Coleman, D. P., Fossett, J. E., Gaudette, N. F., Stanley, A. P., Thomas, B. F., Jeffcoat, A. R.
• Format: Journal Article
• Language: English
• Published: London Informa UK Ltd 01.06.2001; Taylor & Francis
• Subjects: Administration, Cutaneous; Administration, Inhalation; Administration, Oral; Alkynes - administration & dosage; Alkynes - pharmacokinetics; Alkynes - urine; Animals; Bile - metabolism; Biological and medical sciences; Breath Tests; Carbon Radioisotopes; Chemical and industrial products toxicology. Toxic occupational diseases; Chromatography, High Pressure Liquid; Feces; Injections, Intravenous; Kinetics; Male; Mass Spectrometry; Medical sciences; Mice; Propanols - administration & dosage; Propanols - pharmacokinetics; Propanols - urine; propargyl alcohol; Rats; Rats, Inbred F344; Tissue Distribution; Toxicology; Various organic compounds; Intravenous administration; Rat; Rodentia; Oral administration; Metabolism; Inhalation; Percutaneous route; Toxicokinetics; Vertebrata; Mammalia; Mouse; Animal; Distribution; Pharmacokinetics
• ISSN: 0049-8254; 1366-5928
• DOI: 10.1080/00498250110053228

1. The disposition of propargyl alcohol (PAL) radiolabelled with carbon-14 ([2,3- 14C]PAL) was determined in the F344 rat and B6C3F1 mouse following intravenous (i.v.), oral, inhalation and dermal exposure. 2. By 72 h following an i.v. (1 mg kg -1) or oral (50 mg kg-1) dose, 76-90% of the dose was excreted. Major routes of excretion by rat were urine (50-62%), CO2 (19-26%) and faeces (6-14%). Major routes of excretion by mouse were urine (30-40%), CO2 (22-26%) and faeces (10-20%). Less than 6% of the dose remained in tissues at 72 h. Biliary excretion of radioactivity by rat (62% in 4 h) was much greater than elimination in faeces (6% in 72 h), indicating that PAL metabolites underwent extensive enterohepatic recycling. 3. Dermal exposure studies demonstrated that dermal absorption of PAL was minimal due to its inherent volatility. 4. In the inhalation studies (1, 10 or 100 ppm for 6 h), 23-68% of the radioactivity to which animals were exposed was absorbed. The primary route of excretion was urine (23- 53%), and a significant portion was exhaled as volatile organics (15-30%). 5. PAL was extensively metabolized by both species. One metabolite was identified as 3,3-bis[(2-(acetylamino)-2-carboxyethyl)thio]-1-propanol, which is consistent with Banijamali et al. (1999).