Preparation and Evaluation of Ketoprofen Nanosuspension Using Solvent Evaporation Technique

  • Hayder K . Abbas
  • Fatimah M. Hussein Wais
  • Ahmed N. Abood

Abstract

 


 


The effective surface area of drug particle is increased by a reduction in the particle size. Since dissolution takes place at the surface of the solute, the larger the surface area, the further rapid is the rate of drug dissolution. Ketoprofen     is class II type drug according to (Biopharmaceutics Classification System BCS) with low solubility and high permeability. The aim of this investigation was to increase the solubility and hence the dissolution rate by the preparation of ketoprofen     nanosuspension using solvent evaporation method. Materials like PVP K30, poloxamer 188, HPMC E5, HPMC E15, HPMC E50, Tween 80 were used as stabilizers in perpetration of different formulas of Ketoprofen     nanosuspensions. These formulas were evaluated for particle size, entrapment efficiency of drug (EE), effect of stabilizer type, effect of stabilizer concentration and in-vitro dissolution studies. All of the prepared Ketoprofen     nanosuspensions formulas showed a particle size result within Nano range. The average particle size of Ketoprofen     nanosuspensions formulas was observed from 9.4 nm to 997 nm. Entrapment efficiency was ranged from 79.23% to 95.41 %. The in vitro dissolution studies showed a significant (p<0.01) enhancement in dissolution rate of nanosuspension formulas compared to pure drug (drug alone) and physical mixture (drug and stabilizer). The results indicate the suitability of solvent evaporation method for Ketoprofen with improved in vitro dissolution rate and thus perhaps enhance fast onset of action for drug.

Published
Dec 25, 2017
How to Cite
K . ABBAS, Hayder; M. HUSSEIN WAIS, Fatimah; N. ABOOD, Ahmed. Preparation and Evaluation of Ketoprofen Nanosuspension Using Solvent Evaporation Technique. Iraqi Journal of Pharmaceutical Sciences ( ISSN: 1683 - 3597 , ESSN : 2521 - 3512), [S.l.], v. 26, n. 2, p. 41-55, dec. 2017. ISSN 1683-3597. Available at: <http://www.bijps.com/index.php/bijps/article/view/727>. Date accessed: 18 jan. 2018. doi: http://dx.doi.org/10.1234/ijps.v26i2.727.