Modification of the dissolution behaviour of a water-insoluble drug, naftazone, for zero-order release matrix preparation

J Pharm Pharmacol. 1994 Jun;46(6):476-80. doi: 10.1111/j.2042-7158.1994.tb03830.x.

Abstract

The preparation of hydrophilic matrix tablets able to release naftazone, a water-insoluble drug, into an aqueous medium at a constant rate (zero-order dissolution) is described. Enhancement of dissolution rate of the drug was achieved using cross-linked carmellose sodium, beta-cyclodextrin or hydroxypropyl-beta-cyclodextrin. Hypromellose was used as a water-gelling polymer. Tablets could be prepared that released naftazone at a constant rate over 16 h.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calorimetry, Differential Scanning
  • Delayed-Action Preparations / chemistry*
  • Drug Carriers
  • Naphthoquinones / chemistry*
  • Photomicrography
  • Solubility
  • Tablets*
  • Water

Substances

  • Delayed-Action Preparations
  • Drug Carriers
  • Naphthoquinones
  • Tablets
  • Water
  • naftazone