LC478, a Novel Di-Substituted Adamantyl Derivative, Enhances the Oral Bioavailability of Docetaxel in Rats

P-glycoprotein (P-gp)-mediated efflux of docetaxel in the gastrointestinal tract mainly impedes its oral chemotherapy. Recently, LC478, a novel di-substituted adamantyl derivative, was identified as a non-cytotoxic P-gp inhibitor in vitro. Here, we assessed whether LC478 enhances the oral bioavailab...

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Autores principales: Seung Yon Han (Autor), Qili Lu (Autor), Kyeong Lee (Autor), Young Hee Choi (Autor)
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Publicado: MDPI AG, 2019-03-01T00:00:00Z.
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