A novel approach to zero-order constant-rate drug delivery from contact lenses is presented. Quasi-Case II non-Fickian transport is achieved by non-uniform drug and diffusivity distributions within three-layer bimodal amphiphilic conetworks (beta-APCNs). The center layer is a highly oxygen permeable beta-APCN matrix, which contains the drug and exhibits a high drug diffusivity. The outer beta-APCN layers contain no-drug and are loaded with vitamin E, which slows diffusion. In contrast to single-layer neat-polymer and vitamin E-loaded films that display first-order burst kinetics, it is demonstrated experimentally and by modeling that the combined effect of nonuniform distribution of drug loading and diffusion constants within the three-layer lens maintains low local drug concentration at the lens-fluid interface and yields zero-order drug delivery. The release rates of topical antibiotics provide constant-rate therapeutic-level delivery with appropriate oxygen permeability for at least 30 h, at which time approximate to 25% of the drug was released.
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