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Controlled release of isonicontinic acid hydrazide from the membrane-coated tablet

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Abstract

Membrane-coated tablet of isonicotinic acid hydrazide (INAH) which releases INAH at the zero-order kinetics was developed. It consisted of a soluble tablet core surrounded by a porous membrane which controls the diffusion rate. Tablet cores were prepared by compressing granules of INAH and polyvinyl pyrrolidone (PVP). The cores were coated by polyvinyl chloride (PVC) dissolved in methyl ethyl ketone in which micronized sucrose were suspended. Diffusion rate of INAH from the tablet through the membrane was constant until the loaded INAH in the core was almost released. The rate was independent of pH of the dissolution medium. Watersoluble sucrose particles behaved as a poreproducing material in the water-insoluble PVC film coat. The pH independency of the rate was probably due to the high solubility of INAH in the water of wide pH range. The diffusion rate of INAH could be controlled by changing the composition of the membrane or the coat weight. This membrane-coated INAH tablet seemed to be a powerful candidate for the controlled release drug delivery system (DDS) of INAH or other highly watersoluble drugs.

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Literature Cited

  1. Flynn, G.L., Yalkowsky, S.H., and Roseman, T.J.: Mass transport phenomena and model, theoretical concepts.J. Pharm. Sci. 63, 479 (1974).

    Article  PubMed  CAS  Google Scholar 

  2. Borodkin, S., and Tucker, F.E.: Linear drug release from laminate hydroxypropyl cellulose-polyvinyl acetate films.ibid. 64, 1289 (1975).

    Article  PubMed  CAS  Google Scholar 

  3. Lipper, R.A., and Higuchi, W.I.: Analysis of theoretical behavior of a proposed zero-order drug delivery system.ibid. 66, 163 (1977).

    Article  PubMed  CAS  Google Scholar 

  4. Brooke, D., and Washkhun, R.J.: Zero-order drug delivery system, theory and preliminary testing.ibid. 66, 159 (1977).

    Article  PubMed  CAS  Google Scholar 

  5. Källstrand, G., and Ekman, B.: Membrane-coated tablets, a system for the controlled release of drugs.ibid. 72, 772 (1983).

    Article  PubMed  Google Scholar 

  6. Des Prez, R., and Boone, I.V.: Metabolism of14C-isoniazid in humans.Am. Rev. Res. Dis. 84, 42 (1951).

    Google Scholar 

  7. Elemdorf, D.F., Cawthon, W.V., Muschenheim, C., and McDermott, W.: The absorption, distribution, excretion and short time toxicity of isonicotinic acid hydrazide (Nydrazide) in man.Am. Rev. Tuber. 65, 429 (1952).

    Google Scholar 

  8. Barley, J.F., Evered, D.F., and Tromon, S.M.: Transport of isoniazid across small intestine in vitro.Biochem. Pharmacol. 21, 2660, (1972).

    Article  PubMed  CAS  Google Scholar 

  9. Harold, G.B., Ihor, B., Vincent, M., and Stanley, A.K.: Plasma and salivary concentration of isonizid in man, preliminary findings in two slow acetylator subjects.J. Pharmacokin. Biopharm. 3, 443 (1975).

    Article  Google Scholar 

  10. Wendell, W.W., and Dabid, W.H.: Clinical pharmacokinetics of isoniazid.Clin. Pharmackin. 4, 401 (1979).

    Article  Google Scholar 

  11. Jenne, J.W.: Studies of human pattern of isoniazid metabolism using an intravenous fall-off technique with a chemical method.Am. Rev. Res. Dis. 81, 1 (1960).

    CAS  Google Scholar 

  12. Evans, D.A.P., Manley, K.A., and Mckusic, V.A.: Genetic control of isoniazid metabolism in man.Br. Med. J. 13, 485 (1960).

    Article  Google Scholar 

  13. Evans, D.A.P.: Individual variations of drug metabolism as a factor in drug toxicity.Ann. N. Y. Aca. Sci. 123, 178 (1965).

    Article  CAS  Google Scholar 

  14. Peters, J.H., Miller, K.S., and Brown, P.: Studies on the metabolic basis for the genetically determined capacities for isoniazid inactivation in man.J. Pharm. Exp. Ther. 150, 298 (1965).

    CAS  Google Scholar 

  15. Scott, E.M., Wright, R.C., and Weaver, D.D.: The discrimination of phentypes for rates of disapperance of isonicotinoyl hydrazide from serum.J. Clin. Invest. 48, 1173 (1969).

    Article  PubMed  CAS  Google Scholar 

  16. Hearse, D.J., and Weber, W.W.: Multiple N-acetyltransferases and drug metabolism.Biochem. J. 132, 519 (1973).

    PubMed  CAS  Google Scholar 

  17. Ellard, G.A., and Gammon, P.T.: Pharmacokinetics of INAH metabolism in man.J. Pharmacokin. Biopharm. 4, 83 (1976).

    Article  CAS  Google Scholar 

  18. Trimbell, J.A., Wright, J.M., and Baille T.A.: Monoacetyl hydrazine as a metabolite of isonizid in man.Clin. Pharm. Ther. 22, 602 (1977).

    Google Scholar 

  19. Iselius, L., and Evans, D.A.P.: Formal genetics of isoniazid metabolism in man.Clin. Pharmacokin. 8, 541 (1983).

    CAS  Google Scholar 

  20. Ellard, G.A., Gammon, P.T., Lakshminarayan, S., Fox, W., Aber, V.R., Mitchison, D.A., Citron, K.M., and Tall, R.: Pharmacology of some slow-release preparations of potential use in intermittent treatment of tuberculosis.Lancet. 1, 340 (1972).

    Article  PubMed  CAS  Google Scholar 

  21. Jeanes, C.W.L., Schaefer, O., and Edius, L.: Comparative blood levels and metabolism of INAH and an INAH-matrix preparation in fast and slow inactivations.Can. Med. Ass. J. 106, 331 (1972).

    PubMed  CAS  Google Scholar 

  22. Edius, L., Hodkin, M.M., Hsu, A.H.E., and Schaefer, O.: Pharmacokinetic studies with an isoniazid slow-releasing matrix preparation.Am. Rev. Res. 110, 34 (1974).

    Google Scholar 

  23. Chiellini, E., and Giust, P.:Polymers in Medicine, Biomedical and Pharmacological Applications. Plenum Press, New York, N.Y., p. 201 (1983).

    Google Scholar 

  24. idem., p. 375 (1983).

    Google Scholar 

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Kim, K.M., Kim, S.K. Controlled release of isonicontinic acid hydrazide from the membrane-coated tablet. Arch. Pharm. Res. 8, 7–14 (1985). https://doi.org/10.1007/BF02897560

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