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• W2770378584 abstract "A novel quasi-3D (Q3D) modeling approach was developed to model networks of one dimensional structures like tubes and vessels common in human anatomy such as vascular and lymphatic systems, neural networks, and respiratory airways. Instead of a branching network of the same tissue type, this approach was extended to model an interconnected stack of different corneal tissue layers with membrane junction conditions assigned between the tissues. The multi-laminate structure of the cornea presents a unique barrier design and opportunity for investigation using Q3D modeling. A Q3D model of an in vitro rabbit cornea was created to simulate the drug transport across the cornea, accounting for transcellular and paracellular pathways of passive and convective drug transport as well as physicochemistry of lipophilic partitioning and protein binding. Lipophilic Rhodamine B and hydrophilic fluorescein were used as drug analogs. The model predictions for both hydrophilic and lipophilic tracers were able to match the experimental measurements along with the sharp discontinuities at the epithelium-stroma and stroma-endothelium interfaces. This new modeling approach was successfully applied towards pharmacokinetic modeling for use in topical ophthalmic drug design." @default.
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• W2770378584 date "2018-01-01" @default.
• W2770378584 modified "2023-09-26" @default.
• W2770378584 title "Computational modeling of drug transport across the in vitro cornea" @default.
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• W2770378584 doi "https://doi.org/10.1016/j.compbiomed.2017.11.009" @default.
• W2770378584 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5766268" @default.
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