Phosphodiester Conjugation of Metronidazole and Dexamethasone as Possible Mutual Prodrug

Authors

  • Muthana D. Saud
  • Suhair M. Ghani

DOI:

https://doi.org/10.31351/vol15iss1pp80-85

Abstract

As possible mutual prodrug had been synthesized that contain metronidazole and dexamethazone conjugated through phosphodiester linkage. The rationale for this type of conjugate is to get a prodrug with possible site – specific delivery of its active constituents into the lower parts of the G.I.T.

This compound was synthesized by the reaction of dexamethzone – 21 – phosphate with metronidazole to form:(1 – (dexamethazone – 21 – phosphoryl) – metronidazole)

   This conjugate was performed using dicyclohexylcarbodiimide (DCC) as a condensing agent. The identity of the prepared compound had been confirmed using T.L.C., U.V. spectroscopy, IR spectroscopy and elemental analysis.

The partition coefficient for it had also been determined through n – Octanol / water partitioning system.

How to Cite

1.
D. Saud M, M. Ghani S. Phosphodiester Conjugation of Metronidazole and Dexamethasone as Possible Mutual Prodrug. Iraqi Journal of Pharmaceutical Sciences [Internet]. 2017 Apr. 2 [cited 2024 Dec. 19];15(1):80-5. Available from: https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/631

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Published

2017-04-02