Solubility Enhancement of Budesonide and Statistical Optimization of Coating Variables for Targeted Drug Delivery

<table class="table-group" width="800px"><tr class="fig-image" id="a"><td><img alt="262194.fig.003a" src="https://static.hindawi.com/articles/jphar/volume-2014/262194/figures/262194.fig.003a.jpg"/></td></tr><tr class="fig-caption"><td align="center"><table><tr><td><b>(a) </b>BUD</td></tr></table></td></tr><tr class="fig-image" id="b"><td><img alt="262194.fig.003b" src="https://static.hindawi.com/articles/jphar/volume-2014/262194/figures/262194.fig.003b.jpg"/></td></tr><tr class="fig-caption"><td align="center"><table><tr><td><b>(b) </b>PXM</td></tr></table></td></tr><tr class="fig-image" id="c"><td><img alt="262194.fig.003c" src="https://static.hindawi.com/articles/jphar/volume-2014/262194/figures/262194.fig.003c.jpg"/></td></tr><tr class="fig-caption"><td align="center"><table><tr><td><b>(c) </b>Optimized SD (1 : 3)</td></tr></table></td></tr></table>

<table>X-Ray diffractograms of (a) BUD, (b) PXM, and (c) optimized SD (1 : 3).</table>

Journal of Pharmaceutics

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Figure 3

Figure 3: Solubility Enhancement of Budesonide and Statistical Optimization of Coating Variables for Targeted Drug Delivery 