Inversion of optical configuration of alpha-methylfluorene-2-acetic acid (cicloprofen) in rats and monkeys
- PMID: 8287
Inversion of optical configuration of alpha-methylfluorene-2-acetic acid (cicloprofen) in rats and monkeys
Abstract
A simple and sensitive radiometric method to determine the individual enantiomers of cicloprofen has been developed. 14C-Cicloprofen was converted to its L-leucine diastereoisomers, which were separated by thin-layer chromatography and quantified by measuring the radioactivity in the area corresponding to each individual diastereoisomer. This technique has also been used to measure the enantiomers of unlabeled cicloprofen by condensing with 14C-labeled L-leucine. By using the radiometric method, a unique biotransformation process, the inversion of the (-)-enantiomer of alpha-methylfluorene-2-acetic acid to its (+)-enantiomer, has been demonstrated in the rat and monkey. The rate of (-)- to (+)-inversion was found to be faster in the rat than in the monkey. After single or repeated oral adminstration of the racemic modification or the (-)-enantiomer of cicloprofen to both species, the ratio of (+)- to (-)-enantiomers of cicloprofen in plasma, urine, or bile increased with time. At 5, 22, and 48 hr after oral administration of a single 50-mg/kg dose of the (-)-enantiomer, 14C-cicloprofen in rat plasma contained 20, 50, and 79%, respectively, of the (+)-enantiomer. After receiving the same dose of (-)-enantiomer, monkey plasma contained 16.5% and 32% of (+)-enantiomer at 8 and 24 hr, respectively. After oral administration of a single 50-mg/kg dose of the (+)-enantiomer of 14C-cicloprofen to rats and monkeys, the percentage of (-)-enantiomer in plasma varied from 2 to 15%. Since the administered (+)-enantiomer contained 4% of (-)-enantiomer and the (+)-enantiomer was excreted at a faster rate than its (-)-antipode by rats or monkeys, it is not known whether an occasional small percentage increase of (-)-enantiomer in plasma resulted from the (+)-to-(-) inversion, or from faster elimination of the (+)-enantiomer. Nevertheless, if (+)-to-(-) inversion does occur in these two species, the rate is much slower than for the (-)-to-(+) inversion.
Similar articles
-
Metabolism of the (+)-, (+/-)-, and (-)-enantiomers of alpha-methylfluorene-2-acetic acid (cicloprofen) in rats.Xenobiotica. 1977 Sep;7(9):549-60. doi: 10.3109/00498257709038690. Xenobiotica. 1977. PMID: 602253
-
Stereospecific inversion of l-alpha-methylfluorene-2-acetic acid to its d-enantiomer in the dog.Xenobiotica. 1976 Mar;6(3):159-69. doi: 10.3109/00498257609151626. Xenobiotica. 1976. PMID: 1274380
-
Metabolism of alpha-methylfluorene-2-acetic acid (cicloprofen): isolation and identification of metabolites from rat urine.Xenobiotica. 1978 Feb;8(2):121-31. doi: 10.3109/00498257809060391. Xenobiotica. 1978. PMID: 626004
-
Metabolism of p-(cyclopropylcarbonyl)phenylacetic acid (SQ 20,650). Species Differences.Drug Metab Dispos. 1975 May-Jun;3(3):171-9. Drug Metab Dispos. 1975. PMID: 238816
-
Chiral inversion of drugs: coincidence or principle?Curr Drug Metab. 2004 Dec;5(6):517-33. doi: 10.2174/1389200043335360. Curr Drug Metab. 2004. PMID: 15578945 Review.
Cited by
-
Stereospecific inversion of (R)-(-)-benoxaprofen in rat and man.Eur J Drug Metab Pharmacokinet. 1980;5(3):169-72. doi: 10.1007/BF03189461. Eur J Drug Metab Pharmacokinet. 1980. PMID: 7202435
-
High-performance liquid chromatography-tandem mass spectrometry in the identification and determination of phase I and phase II drug metabolites.Anal Bioanal Chem. 2008 May;391(1):59-78. doi: 10.1007/s00216-008-1962-7. Epub 2008 Mar 15. Anal Bioanal Chem. 2008. PMID: 18345532 Free PMC article. Review.
-
Pharmacokinetics of enantiomers of chiral non-steroidal anti-inflammatory drugs.Eur J Drug Metab Pharmacokinet. 1988 Jan-Mar;13(1):1-9. doi: 10.1007/BF03189920. Eur J Drug Metab Pharmacokinet. 1988. PMID: 3294019 Review. No abstract available.
-
Stereoselectivity in clinical pharmacokinetics and drug development.Eur J Drug Metab Pharmacokinet. 1990 Apr-Jun;15(2):109-25. doi: 10.1007/BF03190194. Eur J Drug Metab Pharmacokinet. 1990. PMID: 2200681 Review. No abstract available.
-
Stereoselective disposition of ibuprofen enantiomers in man.Br J Clin Pharmacol. 1985 May;19(5):669-74. doi: 10.1111/j.1365-2125.1985.tb02694.x. Br J Clin Pharmacol. 1985. PMID: 4005104 Free PMC article.