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J Pharm Pharmacol ; 45(7): 614-7, 1993 Jul.
Article in English | MEDLINE | ID: mdl-8105055

ABSTRACT

To investigate whether dogs are able to excrete acetylated drugs by active transport, the plasma kinetics and renal excretion of the N4-acetyl metabolites of sulphasomidine and sulphadimethoxine were studied in the beagle dog after a rapid intravenous bolus injection. Two doses of N4-acetylsulphasomidine (1050 and 105 mg) and one dose of N4-acetylsulphadimethoxine (472 mg) were administered on separate occasions. The renal clearance (CLR) was as follows: N4-acetylsulphasomidine (1050 mg) 34 mL min-1; N4-acetylsulphasomidine (105 mg) 28 mL min-1; and N4-acetylsulphadimethoxine (472 mg) 24 mL min-1. CLR was higher than expected on the basis of the measured glomerular filtration rate, indicating that the N4-acetyl metabolites may be excreted by the renal tubules by active tubular transport. Saturation of the excretion process of N4-acetylsulphasomidine occurred with a transport maximum of 930 +/- 190 micrograms min-1 and a Michaelis-Menten constant of 37 +/- 10 micrograms mL-1. It may be concluded that the dog renal organic anion transport system is able to secrete acetylated sulphonamides.


Subject(s)
Kidney Tubules/metabolism , Sulfadimethoxine/analogs & derivatives , Sulfisomidine/analogs & derivatives , Acetylation , Animals , Chromatography, High Pressure Liquid , Dogs , Glomerular Filtration Rate , Injections, Intravenous , Male , Protein Binding , Regression Analysis , Sulfadimethoxine/blood , Sulfadimethoxine/pharmacokinetics , Sulfadimethoxine/urine , Sulfisomidine/blood , Sulfisomidine/pharmacokinetics , Sulfisomidine/urine
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