Novel formulations of dipyridamole with microenvironmental pH-modifiers for improved dissolution and bioavailability under hypochlorhydria

Int J Pharm. 2012 Sep 15;434(1-2):148-54. doi: 10.1016/j.ijpharm.2012.05.040. Epub 2012 May 27.

Abstract

This study was undertaken to develop new dipyridamole (DP) formulations with acidic microenvironmental pH-modifiers for improving dissolution and absorption under hypochlorhydric conditions. Dipyridamole granules (DPG) with ten acidic pH-modifiers were prepared with conventional wet granulation, and their manufacturability, stability and dissolution behavior were characterized. Pharmacokinetic profiling of the optimized DPG with acid was carried out in omeprazole-treated rats as a hypochlorhydric model. On the basis of the manufacturability, stability and dissolution behavior of new DPG formulations, p-toluenesulfonic acid (TS) was found to be a suitable acidic pH-modifier for DPG formulation. Although DPG showed pH-dependent dissolution behavior, DPG with TS exhibited a high rate and extent of dissolution in both acidic and neutral media. After oral administration of DPG (10mg DP/kg) in omeprazole-treated hypochlorhydric rats, there was ca. 40% reduction of the area under the curve of plasma concentration vs. time from zero to 3h (AUC(0-3)) for DPG compared with that in normal rats. However, AUC(0-3) for DPG/TS under hypochlorhydria was almost identical to that of DPG in normal rats. From these findings, the addition of TS as a microenvironmental pH-modifier in DP formulation might be beneficial in expanding the therapeutic potential of DP in hypochlorhydric patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Achlorhydria / metabolism*
  • Administration, Oral
  • Animals
  • Area Under Curve
  • Benzenesulfonates / chemistry*
  • Biological Availability
  • Dipyridamole / administration & dosage
  • Dipyridamole / chemistry
  • Dipyridamole / pharmacokinetics*
  • Disease Models, Animal
  • Drug Compounding
  • Drug Stability
  • Excipients / chemistry
  • Hydrogen-Ion Concentration
  • Male
  • Omeprazole / pharmacology
  • Platelet Aggregation Inhibitors / administration & dosage
  • Platelet Aggregation Inhibitors / chemistry
  • Platelet Aggregation Inhibitors / pharmacokinetics*
  • Rats
  • Rats, Sprague-Dawley
  • Solubility
  • Time Factors

Substances

  • Benzenesulfonates
  • Excipients
  • Platelet Aggregation Inhibitors
  • Dipyridamole
  • Omeprazole
  • 4-toluenesulfonic acid