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Table 1.

Summary of case studies.

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Fig 1.

3D geometry of the human eye with anatomical regions and boundary conditions (B.C) (a) Partially liquefied (PL) VH and (b) VH without PL.

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Fig 2.

Vitreous concentration–time profiles for ranibizumab under four studies, compared with computational data from Zhang et al. (2018) [20].

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Table 2.

Calculated ranibizumab vitreous half-lives in days.

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Table 3.

Predicted intravitreal half-life of ranibizumab for different intravitreal injection locations.

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Fig 3.

Drug concentration in the human macula and VEGF-suppression threshold.

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Fig 4.

Pressure distribution and Darcy flow streamlines in the vitreous humor.

The liquefied region is a sphere for (a) radius mm located at mm, (b) radius mm located at mm, and (c) radius mm located at mm.

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Fig 5.

Sensitivity of drug concentration to diffusion coefficient () (a) Drug concentration-time profile in vitreous humor (b) Drug concentration-time profile in macula using domain vs point probe.

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Fig 5 Expand

Fig 6.

Sensitivity of drug concentration for varying hydraulic conductivity (K) values (a) Drug concentration-time profile in vitreous humor(VH) (b) Drug concentration-time profile in macula using domain vs point probe.

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