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. 2021 May 5;13:25158414211012797. doi: 10.1177/25158414211012797

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© The Author(s), 2021

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).

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Figure 2. — Pharmacokinetic parameters of loteprednol etabonate in New Zealand white rabbit cornea and conjunctiva.¹² The mean ± SEM loteprednol etabonate (a) C_max and (b) AUC_0–12h for rabbits receiving a single ocular dose of loteprednol etabonate ophthalmic suspension 0.5% or loteprednol etabonate MPP suspension 0.4% is depicted. AUC_0–12h, area under the concentration–time curve from time 0 to 12 hours; C_max, maximum concentration; MPP, mucus-penetrating particle; SEM, standard error of the mean.