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. 2021 Aug 2;28(1):1664–1672. doi: 10.1080/10717544.2021.1960928

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© 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 9. — Lymphatic absorption of TG-drug. (A) The volume of lymph collected per hour after intragastric administration in female rats; (B) Cumulative lymphatic transport of Scu-Me-C5-TG and Scu-Me-C5-βMe-TG following intragastric administration to anesthetized mesenteric lymphduct-cannulated female rats; (C) Plasma concentrations of free Scu vs. time following oral administration of Scu (25 mg/kg), Scu-Me-C5-TG (62.5 mg/kg equivalent dose of Scu), and Scu-Me-C5-βMe-TG (62.5 mg/kg equivalent dose of Scu) to female rats. *p < .05, **p < .01, ^###p < .001. (data are represented as mean ± SD, n ≥ 3).