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Pharmacokinetics of talniflumate, a prodrug of niflumic acid, following oral administration to man

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Abstract

Plasma profile of niflumic acid following oral administration of talniflumate tablets (Somalgen) was compared to that of niflumic acid tablets in man. Plasma niflumic acid was assayed by HPLC method. Plasma niflumic acid profile from the talniflumate tablets was similar to that from the niflumic acid tablets resulting in no differences in AUC,C max,t max and MRT. It demonstrates that talniflumate is a prodrug of niflumic acid, and undergoes extensive first-pass biotransformation to niflumic acid. However, plasma niflumic acid concentration at 30 min after talniflumate dosing was significantly (p<0.05) higher than that of niflumic acid dosing. The more potent analgesic activity of talniflumate than niflumic acid might be related to this higher plasma drug concentration at the earlier phase. Considering that talniflumate is less irritant to gastrointestinal mucosa than niflumic acid, talniflumate seems to be advantageous over niflumic acid in therms of activity and side effects.

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References Cited

  • Avgerinos, A. and Malamataris, S., High performance liquid chromatographic determination of niflumic acid in human plasma and urine.J. Chromatogr., 533, 271–274 (1990).

    Article  PubMed  CAS  Google Scholar 

  • Grossman, A. and Besser, G.M., Prolactinomas.Br. Med. J., 290, 182–184 (1985).

    Article  CAS  Google Scholar 

  • Kim, H. J., Pharmacokinetics of talniflumate, a prodrug of niflumic acid, following oral administration to human. MS theis, College of Pharmacy, Seoul National University, 1994.

  • Lan, S. J., Chando, T. J., Weliky, I. and Schreiber, E. C., Metabolism of niflumic acid-14C: absorption, excretion and biotransformation by human and dog.J. Pharmacol. Exp. Ther., 186, 323–330 (1973).

    PubMed  CAS  Google Scholar 

  • Lancranjan, I., The endocrine profile of bromocriptione: its application in endocrine diseases.J. Neural. Transm., 51, 61–82 (1981).

    Article  PubMed  CAS  Google Scholar 

  • Los, M., Boned, J. E. and Piccininali, C., Nuevos esteres de acidos anilinonicotinicos Y N-fenilantranilicos sustituidos (New esters of substituted anilinonicotinic and phenylanthranilic acids).Farmaco. Ed. Sci., 36, 372–385 (1981).

    CAS  Google Scholar 

  • Martindale,The Extra Pharmacopoeia. The Pharmaceutical Press, London, 29th ed., 1989, p. 31.

    Google Scholar 

  • Nightingale, C. H., French, M. A. and Quintiliani, R., Cephalosporin pharmacokinetics in beta-lactam antibiotics, ed. by Muranishi, S., Japan Scientific Societies Press, (1981). pp.259–298.

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Kim, HJ., Han, YH., Chung, SJ. et al. Pharmacokinetics of talniflumate, a prodrug of niflumic acid, following oral administration to man. Arch. Pharm. Res. 19, 297–301 (1996). https://doi.org/10.1007/BF02976244

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  • DOI: https://doi.org/10.1007/BF02976244

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