Abstract

The purpose of this study was to investigate the influence of electrolyte type, pH, temperature and aging on the viscosity property of okra gum using paracetamol as model drug. Paracetamol (125 mg/ 5 mL) suspension containing okra gum particles of undersize 180 µm as suspending agent was formulated. Similar suspension of paracetamol was formulated using tragacanth gum as a suspending agent for comparison. Effect of electrolyte type, pH, temperature and aging on the viscosity property of okra gum in paracetamol suspension was evaluated using standard methods. Addition of electrolytes, changes in pH, increase in temperature and increase in storage time were shown to decrease the viscosity of the paracetamol suspension. The effect of temperature and aging on the viscosity of the suspension formulation containing okra gum was more pronounced than on the formulation containing tragacanth gum. Conversely, the effect of alkaline pH and type of electrolyte on the viscosity of the suspension formulation containing tragacanth gum was more pronounced than on the formulation containing okra gum. On the basis of these, formulators and caregivers may consider these factors when designing or using pharmaceutical suspensions containing natural gums such as okra and tragacanth as viscosity enhancing agents.

Highlights

  • IntroductionViscosity of a pharmaceutical suspension is of great importance because it affects stability, redispersibility, drug release and pourability of a suspension[2]

  • Viscosity is termed as resistance to flow[1]

  • The viscosity of the suspension containing tragacanth gum was more affected by alkaline pH than acidic pH; dropping by 4.90 % and 3.24 % respectively

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Summary

Introduction

Viscosity of a pharmaceutical suspension is of great importance because it affects stability, redispersibility, drug release and pourability of a suspension[2]. A good suspension should have adequate viscosity to ensure that the dispersed drug particles remain suspended long enough to maintain stability[3]. A good suspension should have reasonable viscosity to ensure that drug release process is not impeded. A study by Venkateswarlu, Chnadrasekhar and Ramachandra[4] found out that drug release from flucloxacillin suspension decreased as viscosity increased due to formation of high viscosity regions on the layer surrounding drug particles and in the bulk medium due to reduced diffusion process caused by hydrated polymer chains. Adequate viscosity ensures the caregiver is able to pour the suspension from the packaging container without difficult during administration

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