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. 2021 Apr 17;21(2):169–178. doi: 10.1007/s40268-021-00340-9

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© The Author(s) 2021

Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

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Fig. 2 — Schematic of pharmacokinetic model. One-compartment pharmacokinetic model with absorption for oral administration of selenite. Following absorption (k_a), the exogenous dose is distributed into the systemic circulation (central compartment) from where it is eliminated (CL/V). Baseline comprises endogenous selenium levels