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. Author manuscript; available in PMC: 2019 Aug 28.
Published in final edited form as: J Control Release. 2018 Jun 12;284:112–121. doi: 10.1016/j.jconrel.2018.05.037

Figure 1.

Figure 1.

Predicted strength of binding affinities of different cyclodextrins and dextrans to the different corticosteroids performed with Autodock Vina. Lower values represent a stronger binding affinity between the cyclodextrin and the respective corticosteroid. A cyclodextrin diameter dependant increase in affinity is predicted from the docking simulations. Triamcinolone is predicted to bind the strongest with all polymer types.