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. 2019 Oct 28;20(21):5368. doi: 10.3390/ijms20215368

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© 2019 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

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Confocal images of (a) MDCK and (b) MDA-MB-231 treated with PTX loaded L-PD at different incubation times (0 h, 0.5 h, 1 h, 3 h, and 5 h) stained with a Lysotracker (green) and SYTO 61 (red). (c) Flow cytometric (FACS) analysis of in vitro quantitative fluorescence behavior of MDCK and MDA-MB-231 after treatment without (control) and with PTX loaded L-PD. (Scale Bar: 40 µm).

Confocal images of (a) MDCK and (b) MDA-MB-231 treated with PTX loaded L-PD at different incubation times (0 h, 0.5 h, 1 h, 3 h, and 5 h) stained with a Lysotracker (green) and SYTO 61 (red). (c) Flow cytometric (FACS) analysis of in vitro quantitative fluorescence behavior of MDCK and MDA-MB-231 after treatment without (control) and with PTX loaded L-PD. (Scale Bar: 40 µm).