Enhancement of dissolution behavior of aceclofenac by complexation with β-cyclodextrin-choline dichloride coprecipitate
- Publication Type:
- Journal Article
- Journal of Dispersion Science and Technology, 2011, 32 (10), pp. 1477 - 1484
- Issue Date:
|Enhancement of Dissolution Behavior of Aceclofenac by Complexation with Cyclodextrin Choline Dichloride Coprecipitate.pdf||Published Version||797.88 kB|
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The objective of the present investigation was to study the effect of presence of choline dichloride (CDC) in β-cyclodextrin (β-CD) on in vitro dissolution of aceclofenac (AF) from molecular inclusion complexes. The molecular inclusion complexes of AF with β-CD coprecipitated with CDC in 1:1 and 1:2 M ratio were prepared using kneading method. In vitro dissolution of pure drug, physical mixtures, and cyclodextrin inclusion complexes (AF-β-CD-CDC) were carried out. Molecular inclusion complexes of aceclofenac with coprecipitated β-CD showed considerable increase in the dissolution rate in comparison with physical mixture and pure drug in 0.1 N HCl, pH 1.2 and phosphate buffer, pH, 7.4. Inclusion complexes with 1:2 M ratio showed maximum dissolution rate in comparison to other ratios. FTIR spectroscopy and differential scanning calorimetry studies indicated no interaction between AF and β-CD-CDC in complexes in solid state. Dissolution enhancement was attributed to the formation of water soluble inclusion complexes with the precipitated form of b-CD. The in vitro release from all the formulations was best described by first order kinetics (R2 =1/4 0.9354 and 0.9268 in 0.1 N HCl and phosphate buffer, respectively) followed by Higuchi release model (R2 =1/4 0.9029 and 0.9578 in 0.1 N HCl and phosphate buffer, respectively). In conclusion, dissolution of aceclofenac can be enhanced by using the β-CD-CDC coprecipitate as a host molecule. © Taylor & Francis Group, LLC.
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