Solubility and Dissolution Improvement of Aceclofenac using Different Nanocarriers

Journal of Bioequivalence & Bioavailability 01/2009; 01(02). DOI: 10.4172/jbb.1000007
Source: DOAJ

ABSTRACT The aim of the present investigation was to improve solubility and dissolution of the lipophilic drug aceclofenac using three nanocarriers namely nanoemulsion, solid lipid nanosuspension and polymeric nanosuspension. The solubility of aceclofenac in distilled water and different nanocarriers was determined using the UV spectrophotometer method at the wavelength of 274 nm. Dissolution studies of pure aceclofenac suspension and its nanocarriers were performed using USP dissolution apparatus in distilled water. The highest solubility (198.53 mg/ml) as well as % dissolution (99.5) of aceclofenac was obtained with nanoemulsion formulation as comparedto lipid and polymeric nanosuspension. The results of solubility and dissolution were highly significant in nanoemulsion as compared to lipid and polymeric nanosuspension (P<0.01). Dissolution profile of aceclofenac in lipid and polymeric nanosuspension was significant as compared to pure aceclofenac suspension (P<0.05). These results indicated that nanoemulsion is a promising nanocarrier as compared to lipid and polymeric nanosuspension for solubility and dissolution enhancement of aceclofenac.

Download full-text


Available from: Sheikh Shafiq, Sep 26, 2015
363 Reads
  • Source
    [Show abstract] [Hide abstract]
    ABSTRACT: Purpose: To measure the extent of solubility of the lipophilic drug, aceclofenac, in 13 oils as well as its in vitro permeability from these oils in order to develop optimized topical microemulsion and microemulsion-based gel for improved bioavailability. Methods: UV spectrophotometeric method was used at the wavelength of 276 nm to measure the dissolved quantity of aceclofenac in each of the oils (almond oil, oleic acid, castor oil, paraffin oil, cinnamon oil, clove oil, canola oil, sesame oil, isopropyl myristate (ipm), sunflower oil, corn oil, coconuts oil and eucalyptus oil) at 25 °C. The in-vitro permeability of aceclofenac in each of these oils was determined at 32 ± 0.5 °C using Franz diffusion cell with phosphate buffer (pH 7.4) as medium with 0.45 μ cellulose acetate membrane. The solubility and permeability of aceclofenac were compared with the hydroalcoholic solution of aceclofenac. Results: The highest solubility values of 9.153 and 8.560 mg/ml for aceclofenac were obtained with almond oil and oleic acid, respectively (p < 0.05). However the solubility and permeability of aceclofenac in hydro-alcoholic solution were 150.65 mg/ml and 14.91± 0.05 μg/cm2/h, respectively. Aceclofenac also showed higher permeability values (1.45± 0.04 and 1.21 ± 0.06) in almond oil and oleic acid, respectively, than in the other oils (p < 0.05). Conclusion: These findings show that almond oil and oleic acid are promising vehicles for aceclofenac as its enhanced solubility and permeability in these vehicles are suggestive of improved bioavailability. Keywords: Aceclofenac, Almond oil, Solubility; Permeability, Oleic acid, Bioavailability.
    Tropical Journal of Pharmaceutical Research 03/2014; 13(3):327-330. DOI:10.4314/tjpr.v13i3.2 · 0.50 Impact Factor
  • Source