Literature DB >> 1195117

Enterohepatic circulation of tetracycline in rats.

J Adir.   

Abstract

The absorption of tetracycline hydrochloride excreted in the bile of rats was evaluated using the insitu intestinal preparation. For comparative purposes, the absorption of the drug from an aqueous solution having the same pH as that of the bile was also determined. After 4 hr, the amounts of tetracycline absorbed from the bile and aqueous solutions were 72.92 and 77.34%, respectively. There was no significant difference in the amount of drug accumulated in the gut tissue. The disappearance of the drug from the intestinal lumen was biexponential, and the kinetic parameters appeared to be similar. It was concluded that tetracycline excreted in the bile is readily absorbed from the rat intestine. Accordingly, biliary excretion does not seem to account for a significant elimination of this antibiotic from the body.

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Year:  1975        PMID: 1195117     DOI: 10.1002/jps.2600641121

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  3 in total

Review 1.  Multiple peaking phenomena in pharmacokinetic disposition.

Authors:  Neal M Davies; Jody K Takemoto; Dion R Brocks; Jaime A Yáñez
Journal:  Clin Pharmacokinet       Date:  2010-06       Impact factor: 6.447

2.  Controlled release of tetracycline--III: A physiological pharmacokinetic model of the pregnant rat.

Authors:  L S Olanoff; J M Anderson
Journal:  J Pharmacokinet Biopharm       Date:  1980-12

3.  Pharmacokinetics of a Long-Acting Formulation of Oxytetracycline in Freshwater Crocodiles (Crocodylus siamensis) after Intramuscular Administration at Three Different Dosages.

Authors:  Saranya Poapolathep; Narumol Klangkaew; Napasorn Phaochoosak; Tara Wongwaipairoj; Mario Giorgi; Narongsak Chaiyabutr; Darren J Trott; Amnart Poapolathep
Journal:  Animals (Basel)       Date:  2020-07-27       Impact factor: 2.752

  3 in total

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